Recent Advances Towards Syntheses of Diterpenoid Alkaloids

Abstract The diterpenoid alkaloids serve as a rich source of synthetic targets for organic chemists, due to the intriguing structure of the overlapping ring systems, along with biological activities commonly associated with compounds of this group. Fifteen total syntheses and numerous synthetic studies towards construction of ring fragments have been reported since 2010. This review article gives a brief overview of diterpenoid alkaloids and summarizes the recent synthetic efforts. 1 Introduction 1.1 Structural Classification and Biosynthetic Origin 1.2 Structure Elucidation of the Aconitum Alkaloids 2 Total Syntheses 2.1 C18-Diterpenoid Alkaloids 2.2 C19-Diterpenoid Alkaloids 2.3 C20-Diterpenoid Alkaloids 3 Strategies To Synthesize Ring Systems 3.1 Radical-Based Cyclizations 3.2 Ruthenium-Mediated Enyne Cycloisomerization 3.3 Reductive Coupling 3.4 Diels–Alder Reactions 3.5 Oxidative Dearomatization/Diels–Alder Sequence 3.6 Transannular Aziridation 3.7 Intramolecular [5+2] Cycloaddition 3.8 Miscellaneous 4 Conclusion

Key words diterpenoids, alkaloids, total synthesis, aconitine, natural products 1 Introduction The diterpenoid alkaloids (C 18 , C 19 , and C 20 ) are a group of chemically and structurally complex natural products that possess a long list of pharmaceutical properties. 1 This list includes, but is not limited to, anti-inflammatory, analgesic, and antiarrhythmic properties. 2 Most of these properties are reported to be derived from interactions between the natural products and voltage-gated ion channels, particularly potassium and sodium channels. 3 While researchers worldwide are still discovering new compounds within this class from numerous plant species, these pseudoalkaloids have been traditionally linked to the Aconitum, Consolidum, and Delphinium genus of plants, from which they were extracted and used in traditional medicine. However, research into broader applications still continues. 4 The most common uses included the treatment of cardiovascular diseases and as an analgesic.

Structural Classification and Biosynthetic Origin
The diterpenoid alkaloids family is generally grouped by key conserved structural features and size of the carbon scaffolds. The smallest of the three main groups are the C 18diterpenoid alkaloids, with over 50 discrete compounds already known. 2b These C 18 -diterpenoid alkaloids can be further subdivided into two distinct types; the lappaconitinetype 1, and the ranaconitine-type 2 (Figure 1) with the major difference being the presence of the additional oxygenation at the C7 position in the ranaconitine core. The C 19 -diterpenoid alkaloids are the largest of the three groups and represent over 600 fully characterized molecules. 1c They are structurally closer to the C 18 -diterpenoid core, with the variation being an additional carbon at the piperidine ring junction. This group is divided into 6 unique types, with the aconitine-3 and lycoctonine-type 4 seemingly the most prevalent in Nature (Figure 2). The other Ken-Loon Choo (leftmost) received his B.Sc. degree with honors from the University of Toronto. He then ventured into the oleochemical industry as a research chemist developing a process to synthesize high purity sulfonated fatty acid esters. In 2016, he returned to pursue a graduate degree in the laboratories of Prof. Mark Lautens at the University of Toronto with interest in catalytic asymmetric reactions and total synthesis.
Despite this vast structural diversity amongst the three groups, these natural products are all derived through biosynthetic insertion of the nitrogen into the mature diterpene scaffolds, which then undergoes further elaborations leading to the final product, as shown in Scheme 1. 5 An enzyme-catalyzed cyclization of geranyl-geranyl pyrophosphate affords the ent-copalyl pyrophosphate, which then undergoes a series of transformations, including a critical Wagner-Meerwein rearrangement, affording the ent-kaurane 23 and ent-atisane 24 diterpene skeletons. These scaffolds then undergo amination to form the two main branching points, the veatchines 14 and the atisines 7, notably these can interconvert through a [1,2]-sigmatropic rearrangement. 1,2b,5 Through a series of elegant manipulations by Nature, these cores are later transformed into the numerous natural products observed. Some examples of these are the napellines 15 and denudatines 8, which are accessed through C7-C20 bond formation from the veatchines 14 and atisines 7, respectively. In other cases, after the requisite transformations, the scaffold may fragment to access the smaller core, as seen with the denudatines en route to the C 19  The C 18 -and C 19 -diterpenoid alkaloids have been of great interest to civilizations since antiquity. Preparations from members of the genera Aconitum and Delphinium have been used for such diverse applications as traditional Chinese medicine to surreptitious homicide, aconitine (27) being the most toxic; LD 50 in mice (mg/kg: 0.166, i.v., 0.328 i.p.). 6 However, due to the complexity of these molecules, very little progress beyond isolation was achieved for almost a century. The first published studies into the chemistry of aconitine did not appear until 1894 7 with additional data published in 1895. 8 Following a 29 year hiatus, three additional papers were published in the German literature . 9 British researchers were also immersed in the aconitine problem, between 1894-1937, twelve papers related to structure determination were published by the Royal Society of Chemistry. 10 In this time period, only one paper was published in the North American literature. 11 Despite much information being obtained about occurrence and activities, little was known about the detailed structure due to the limited capabilities of the classical methods of analysis.
This situation changed with the introduction of UV and IR spectroscopy 12 and later, NMR. 13 Due to their less complex structure, the C 20 alkaloids were the initial focus of at-tention. S. W. Pelletier and W. A. Jacobs made many contributions to the structural elucidation, both by chemical and spectroscopic means. 14 A partial synthesis of atisine (28), isoatisine (29), and dihydroatisine (30) was achieved in 1956. 15 The pioneer in the field of detailed structure determination and total synthesis of the Delphinium alkaloids was Karel Wiesner (1919Wiesner ( -1986. He arrived at the University of New Brunswick in 1948 determined to clear up the 'hopeless confusion' surrounding the structure. However, a review indicated that this had been tried many times in the past to no avail. He thus concluded that the best way to approach the problem would be to solve the structure of the more straightforward C 20 members of the class. 16 In the period 1948-1975, several total syntheses were achieved, employing 1 st through 4 th generation methods (Table 1, Figure  4). Some more recent syntheses are included in Table 1. Wiesner published two reviews of his work. 17 Notably, even today, the total synthesis of the fully oxygenated, most complex members of the family, aconitine (27), and beiwutine (31) remain elusive. This article covers advances in total synthesis towards diterpenoid alkaloids from 2010 onwards after excellent coverage of the field by other review articles. 5,18 Figure 5 depicts structurally unique diterpenoid alkaloids that have been synthesized since 2010, such as salviamine E (32) and F (33); 19

Total Synthesis of Neofinaconitine
This convergent total synthesis of neofinaconitine (47) by Shi, Tan, and co-workers in 2013 was designed to begin with an intermolecular Diels-Alder cycloaddition between the in situ generated diene from enone 69 and cyclopropene 70 (Scheme 2). 27 To allow for this strategy, the cyclopentenone intermediate 69 was prepared from commercially available furfuryl alcohol, 58 while the cyclo-

Review Syn thesis
propene starting material 70 was prepared in 6 steps from methyl acrylate. 59 Notably, due to the rapid Alder-ene dimerization of the cyclopropene intermediate, this compound was isolated and was used immediately in the cycloaddition reaction. The Diels-Alder cycloaddition was conducted by addition of intermediate 70 directly to the in situ prepared diene from intermediate 69. Importantly, it was reported that attempts at isolating the enolization-silylation 60 product of 69 led to a difficult-to-control mixture of dimerized cyclopentadiene. Nonetheless, this direct addition to the in situ prepared diene allowed access to the desired product 71 as an inseparable mixture of diastereo-mers (1:1.6). Given that the major diastereomer was the desired product, this mixture was taken through the next four steps to access intermediate 73 (39% over 6 steps). A series of functional group manipulations on intermediate 73 afforded access to diene 75 and set up the second intermolecular Diels-Alder cycloaddition between 75 and 76 catalyzed by SnCl 4 . 27 This is notably an essential step as it afforded a key intermediate 77 as a single diastereomer in excellent yield (87%). This was then converted into the precursor for the Mannich-type N-acyliminium cyclization by the selective oxidation of the exocyclic olefin to afford a carbonyl and followed by elimination of the -bromide to form the

Review
Syn thesis enone 78. The Mannich-type N-acyliminium cyclization was achieved by treatment of intermediate 78 with Tf 2 NH, thereby forming the C11-C17 bond, but was unfortunately also followed by the formation of the cyclic enol ether to form 79 (75%). To overcome this undesired, but unavoidable, formation of the enol ether, a rather nifty trick was employed, a leaving group was introduced at the C3 position by treatment of 79 with CAN, followed by MsCl/Et 3 N in two steps, which was fortunately accompanied by the elimination to afford the dienone 80 (66%, two steps). 27 The last of the keys steps was completed by an intramolecular radical cyclization of dienone 80 in excellent yield to afford the completed neofinacotine scaffold 81 (99%). Finally, installation of the C8 hydroxyl functionality was achieved via a highly strained enone, allowing for a spontaneous nucleophilic attack by water to give 82 and complete the structural requirements. Over an additional 8 steps, the remaining modifications and tailoring were accomplished to afford the total synthesis of racemic neofinaconitine (47). 27 This divergent approach by Shi, Tan, and co-workers was achieved in 30 longest linear steps and afforded racemic neofinaconitine (47) from readily available materials. 27 It should be noted that this strategy offers numerous opportunities to access other types of the diterpenoid alkaloids and as such should be exploited for the preparation of derivatives of such natural products.

Total Synthesis of Weisaconitine D
The Sarpong group completed the total synthesis of weisaconitine D (48), a ranaconitine-type diterpenoid alkaloid, in 2015 in 30 steps overall (Scheme 3). 28 Starting with a Diels-Alder cycloaddition of diene 85 61 and a cyclopentenone derivative 86, 62 the resulting alkene was reduced to give the basic bicyclic ketone intermediate 87. Preparation of the vinyl triflate by treatment of 87 with LHMDS and phenyl triflimide, followed by Pd(0)-catalyzed cross-coupling with cyanide 63 afforded the ,-unsaturated nitrile 88. This approach allowed the assembly of the A and F rings, and serves as the substrate for their Rh-catalyzed conjugate addition with the lithium boronate 89 to access 90 in 60% yield. Notably, this guaiacol derivative was installed with high diastereoselectivity. This transformation should be well noted as the aryl ring of 90 after several transformations will eventually be fashioned into the C/D ring and, as such, this is an excellent point to diverge/modify the oxidation patterns around these rings in the final diterpenoid alkaloid simply by use of the appropriately substituted arene. The ester group of 90 was selectively reduced over the nitrile functionality, followed by Dess-Martin oxidation of the resulting primary alcohol to give aldehyde 91. The newly formed aldehyde 91 underwent a Wittig olefination, followed by hydration of the nitrile group 64 to provide the carboxamide 92. This carboxamide 92 was then rearranged via a Hofmann rearrangement using (diacetoxyiodo)benzene [PhI(OAc) 2 , PIDA], and the

Review Syn thesis
intermediate isocyanate was trapped with methanol, followed by deprotection to the tert-butyldimethylsilyl group with TBAF to give 93. The primary hydroxyl group was then activated by mesylation and treated with KOt-Bu to form the C19-N bond, thereby fashioning the piperidinyl ring of 94. This key step allowed completion of the A, E, and F rings for the C 18 -diterpenoid alkaloids. In order to set construction of the B, C, and D rings, the MOM protecting group of 94 was cleaved, and the phenol was then subjected to an oxidative dearomatization to afford the dienone 95. By merely heating intermediate 95, it underwent an intramolecular Diels-Alder cycloaddition forming 96. This step effectively allowed access to the C 20 core framework of the denudatine-type diterpenoid alkaloids. As such, this pathway can be viewed as an equally effective route to the denudatine-type diterpenoid alkaloids.
To effect the transformation of the bicyclo[2.2.2] structural motif to the bicyclo[3.2.1] core, the ketone functionality of 96 was stereoselectively reduced. It was postulated that this selectivity is as a result of torsional strain from the -disposed methoxy group of the dimethyl ketal. The ketal protecting group was then hydrolyzed to afford 97. Intermediate 97 was then treated with MOMCl to protect the free secondary hydroxyl group, followed by the diastereoselective reduction of the ketone group to provide alcohol 98. The triflation of alcohol 98, followed by treatment with DBU and DMSO at 120 °C led to a Wagner-Meerwein-type rearrangement and thus completed the B, C, and D rings in 99. 6 While several strategies were explored for a formal hydro-methoxylation of the C15-C16 double bond of 99, it was found that this was best achieved via an epoxide intermediate. They employed a hydroxyl-directed epoxidation from the -face using m-CPBA, followed by alkylation of the tertiary hydroxyl to provide 100. 28 The epoxide was regioselectively opened 65 to give a -disposed secondary alcohol group that was methylated to furnish 101 and thus this completed the D-ring of weisaconitine D. The methoxycarbonyl protecting group was removed, the nitrogen was acylated, and the acetamide was reduced using LiAlH 4 . Finally, removal of the MOM protecting by acid treatment of afforded the final product weisaconitine D (48) in a total of 30 steps. 28 This successful total synthesis of weisaconitine D (48) by the Sarpong group 28 should be viewed as a direct opening to other members of the C 18 -ranaconitine class of diterpenoid alkaloids as well as the C 20 -denudatine types. Importantly, their synthetic plan shows great promise in allowing for the preparation of any number of unnatural analogues of this natural product.

C 19 -Diterpenoid Alkaloids
In contrast to the numerous reports of total syntheses of C 20 -diterpenoid alkaloids, there are only a handful of recent total syntheses of C 19 norditerpenoid alkaloids. The total syntheses of liljestrandinine (52) 28 and (-)-cardiopetaline (53) 67 have been reported by the Sarpong group and Fukuyama, Yokoshima, and co-workers, respectively. The total synthesis of aconitine (27) can be considered a holy grail in organic synthesis due to its intricate, highly oxygenated caged framework. The synthesis of this molecule has remained elusive, and the most recent attempt was reported by Qin, Zhang, and co-workers. 66 Several groups have made strategic efforts towards the construction of the C 19 cores and the reported methodologies will be covered here.

Total Synthesis of Liljestrandinine
The synthesis of liljestrandinine (52) 28 starting from synthon 93 is shown in Scheme 4; dienone 104 was prepared in 7 steps in a similar fashion to the synthesis of weisaconitine D (48). At this point, the stage is set for an intramolecular Diels-Alder reaction. The ketone moiety of the Diels-Alder adduct was then reduced to give the hexacyclic alcohol 105, which was converted into the C 19 -diterpenoid alkaloid liljestrandinine (52) in 9 steps.

Total Synthesis of (-)-Cardiopetaline
Fukuyama, Yokoshima, and co-workers disclosed a novel Wagner-Meerwein rearrangement of a sulfonyloxirane to construct the aconitine skeleton (Scheme 5). 67 Sulfonyloxirane 114 was synthesized from synthetic intermediate 108 en route to their previous reported total synthesis of lepenine. 51 Protection of the hydroxy group of 108 followed by removal of the methoxy groups under reductive conditions with SmI 2 furnished ketone 109. Hydrogenation of the olefin was achieved using Pd(OH) 2 on carbon to afford ketone 110, which was then converted into -phenylsulfanyl ketone 111 via a silyl enolate intermediate. Stereoselective reduction gave a secondary alcohol, which was subsequently acylated to yield 112. The sulfide group was oxidized into a sulfone using Oxone and then base-mediated elimination of the acetate group furnished the vinyl sulfone 113. Stereoselective epoxidation was then carried out with tert-butyl hydroperoxide (TBHP) to give sulfonyloxirane 114 with the appropriate stereoconfiguration for a Wagner-Meerwein rearrangement.

Review Syn thesis
Scheme 5 Total synthesis of (-)-cardiopetaline via the Wagner-Meerwein rearrangement of a sulfonyloxirane Surprising stability was observed with the sulfonyloxirane 114 where the intended rearrangement was not observed even under harsh acidic or thermal conditions. The desired rearrangement was finally realized by applying microwave irradiation at 150 °C in methanol. An alkyl shift first occurred to cleave the oxirane to give alcohol 116. The resulting carbocation was trapped by methanol followed by the extrusion of benzenesulfinic acid to form hexacyclic ketone 117. Reduction of the ketone was carried out immediately due to its instability to give alcohol 118. The total synthesis of (-)-cardiopetaline (53) was completed with heating in aqueous sulfuric acid to unmask the alcohol groups.

Review Syn thesis
In 2017, Fukuyama, Yokoshima, and co-workers published another variant (shown in Scheme 6) of the (-)-cardiopetaline (53) synthesis, which does not require pre-activation of the pivotal hydroxy group. 34 The requisite diol 120 was also synthesized from intermediate 108. 51 The ketone in TBS-protected 119 was stereoselectively reduced to alcohol 120 using alane with pyridine as an additive to prevent damage to the ketal moiety; hydrolysis of the ketal followed by exhaustive hydrogenation afforded diol 120, which was the target for the Wagner-Meerwein rearrangement. A number of reaction conditions were tested to initiate the rearrangement, but it was finally found that p-toluenesulfonic acid produced the desired rearranged product mixture 123. Pivalic acid was crucial for the suppression of the undesired acylation of the diol substrate. Hydrolysis was then carried out to liberate the alcohol groups to give (-)-cardiopetaline (53).

Attempted Total Synthesis of Aconitine
The most recent attempt at the total synthesis of aconitine (27) in 2019 was reported by Qin, Zhang, and co-workers (Scheme 7). 66 The synthesis commenced with the decoration of (-)-(R)-carvone (124) to install the desired substituents on the A ring. Nitrone 126 was generated in situ from Scheme 6 Total synthesis of (-)-cardiopetaline via the Wagner-Meerwein rearrangement of a diol without pre-activation

Review Syn thesis
glyoxylate 125 when treated with N-PMB-hydroxylamine, which then induced an intramolecular [3+2] cycloaddition to give isoxazolidine 127 as a single diastereomer.
Deprotection of the N-PMB group followed by oxidation was achieved using DDQ to give imine 128. Hydrolysis, followed by Krapcho decarboxylation, and selective methylation afforded -hydroxynitrile 129. Subsequent steps, including functional group manipulations and an intramolecular Mannich reaction, were carried out to build the E ring giving aldehyde 130. Addition of the alkyne fragment 131 provided propargyl alcohol 132. Further manipulations provided xanthate 133, which was the substrate required to carry out the key radical cascade for the formation of the BD ring systems. The planned cascade first generates a radical at C11 that subsequently cyclizes on to the C10 acceptor and is finally trapped by the alkyne moiety. Various radical initiating conditions were tested, but only decomposition of the substrate was observed without the formation of the desired cyclized product 135. The success of the cascade may be hampered by the premature interference of the alkyne moiety, the acceptor at C10 may be too distant, as well as the possibility of the formation of nitrogen-centered radicals on the tertiary amine. The final key transformation in the proposed route utilized an aza-Prins cascade to furnish the F ring of aconitine (27). Overall, the reported route achieved the synthesis of the fully functionalized AE ring systems of aconitine (27) in 27 steps with an overall yield of 1.64% from (-)-(R)-carvone (124).

Total Synthesis of Septedine
The first and asymmetric total synthesis of septedine (68) was reported in 2018 by Li and co-workers. 57 Septedine (68)

Review Syn thesis
amide 136, aryldiene 141 was accessible in 5 steps. Iridiumcatalyzed polyene cyclization using the conditions of Carreira gave tricyclic intermediate 143.
Intermediate 146 was prepared in order to perform a Diels-Alder reaction. Surprisingly, treatment of 146 with LHMDS gave cyclized product 147. In a sequence of five steps, the protected secondary alcohol was transformed into a ketone, and several manipulations on C-15 and C-16 led to intermediate 149.
C-H activation of C-7 via Sanford's oxidation conditions and conversion of the vinyl group, via an epoxide, into an aldehyde gave 151. The natural product septedine (68) was obtained through a methylation, ester hydrolysis, and reductive amination which occurred under concomitant condensation. In order to investigate the final steps (reductive amination and N,O-ketalization), 7-deoxyseptedine was prepared from a model substrate (not shown).

Total Synthesis of Azitine
A unified approach to assemble atisine-and hetidinetype diterpenoid alkaloids was presented by Liu and Ma. 55 The total syntheses of azitine (66) and the reported structure of navirine C (156) are shown in Scheme 9. Both syntheses contain a common sequence from nitrile 157 to tetracyclic dinitrile 152 in 10 steps (Scheme 10). Reduction of 152 with LiAlH 4 and Li/NH 3 (liq.) led to the formation of imine 153. The final steps towards natural product azitine (66) were a deprotection, olefination, and subsequent allylic oxidation. The other synthesis accomplished from tetracyclic dinitrile 152 started with the formation of the bond between C-20 and C-14 under Shenvi's conditions to give cyclized product 154. A further six steps were required to obtain a structure that was reported to be the natural product navirine C (156), but the spectroscopic data differed from the reported data after isolation.
Scheme 10 Synthesis of the common intermediate for the total syntheses of azitine and the proposed structure of navirine C

Review Syn thesis
168, which was transformed into phenol 169 in five steps. Oxidative dearomatization and intramolecular Diels-Alder cycloaddition was followed by hydrogenation, olefination, and cleavage of an acetal group to give enone 170. This intermediate was previously used by Pelletier and coworkers, and therefore this constitutes a formal synthesis of (±)-atisine (28). 15,68 Scheme 11 Oxidative dearomatization/intramolecular Diels-Alder cycloaddition cascade for the synthesis of (±)-atisine

Synthesis of the Hetidine Scaffold and Total Synthesis of Dihydroajaconine and Gymnandine
A bioinspired synthetic approach to the skeleton of the C 20 -diterpenoid alkaloid type hetidine was presented by Qin, Liu, and co-workers; 53,69 Scheme 12 outlines the synthetic path. Starting from 172, 39,40 alkene 174 was obtained in 5 steps. Then, a Corey-Seebach reaction followed by the well-established oxidative dearomatization and intramolecular Diels-Alder cascade were performed to obtain intermediate 176. The synthesis of this intermediate also concluded the synthesis of the pentacyclic atisine skeleton.
Intermediate 177 was treated with MeMgBr, the dithiane moiety was removed by reaction with Dess-Martin periodinane, and the resulting ketone was reduced to give diol 178. Deacetylation and subsequent amide formation gave intermediate 179, featuring the requisite C-7 hydroxy group and an o-aminobenzamide moiety. Aminal 181 was obtained after reaction with NaNO 2 , CuCl, and HCl/Et 2 O reported by Weinreb and co-workers. 70 A radical mechanism was postulated that proceeds via diazotization and a 1,5-H shift to form intermediate 181, which has the ajaconine skeleton. Cyclization to give the desired hetidine-type product 183 was achieved by an aza-Prins reaction. Throughout the investigations, additional unwanted heptacyclic products were prepared (not shown).

Review Syn thesis
Pentacyclic intermediate 177 was also used by Qin, Liu, and co-workers as starting point for the syntheses of dihydroajaconine (60) and gymnandine (62) (Scheme 13). 53 Precursor 186 was subjected to the method developed by Weinreb and co-workers. 70 Hemiaminal 187 was then successfully transformed into the atisine-type alkaloid diterpenoid dihydroajaconine (60) in 4 steps.
Simultaneous cleavage of the amide C-N bond and the aminal C-O bond of aminal 188 gave cyclic imine 191 in excellent yield. Oxidation of the secondary alcohol, as described by Iwabuchi and co-workers, 71 and cyclization promoted by SmI 2 and subsequent N-acetylation gave the hexacyclic intermediate 192 featuring the denudatine core. After construction of the carbon skeleton, natural product gymnandine (62) was obtained after six additional synthetic steps.

Total Synthesis of Cossonidine
The Sarpong group chose the hydrindanone 87 4a,28,52 as the entry point to their synthetic strategy (Scheme 14). They had previously enjoyed success towards the C 18 -diterpenoid alkaloids scaffold, as well as the preparation of the 6-7-6 fused tricyclic core 72 of the hetidine-and hetisinetypes using this compound as a starting point. 56 In order to convert the ester into an aldehyde, 87 was treated with LiAlH 4 , which led to the reduction of both the ester and ketone functionalities; Ley oxidation 73 75 to afford the -keto ester 197, which was followed by an aryne insertion assisted by CsF to provide intermediate 199. So as to later functionalize the C6 position, a deallylation reaction was performed 76 using catalytic Pd(PPh 3 ) 4 and PhSiH 3 to afford the carboxylic acid 200, which was then treated with 1,3-diiodo-5,5-dimethylhydantoin (DIH, 201) under photochemical conditions to achieve oxidative decarboxylation, 77 and thus leave the C6 carbon as an internal olefin. The methyl group at C4 was installed by deprotection of the primary alcohol, followed by oxidation, then direct conversion into nitrile 203, which then directed the diastereoselective methylation of 203 leading to intermediate 204.
This key intermediate bearing handles at C6 and C20 was now set up for formation of the piperidinyl ring. Treatment of 204 with a cobalt boride (Co 2 B) and borane-tert-butylamine complex, 78 80 to give the structural core 208. The selective cleavage of the C1 methyl ether was carried out using HBr/AcOH, followed by treatment with K 2 CO 3 in methanol to yield the free alcohol 209. Next, a standard Wittig methylenation was carried out to convert the ketone of 209 into an exocyclic methylene 210, and thus completing the C 20 carbon scaffold for the hetisine-type skeleton. A sequence of oxidation/reduction was then utilized to invert the stereochemistry at the C1 position affording 212, which simply left a selenium dioxide oxidation to furnish the allylic alcohol and the final product cossonidine (67). 56

Total Synthesis of Lepenine
The strategy employed by Fukuyama and co-workers in 2014 focused on expanding from the scaffold of tetralone 218, which was accessed over 8 steps starting from L-lactic acid methyl ester and guaiacol (213) in excellent yields (Scheme 15). 51 Having established a successful route to the tetralone, the ketone was then transformed into the diene 219 through a Grignard addition to the ketone followed by silver triflate mediated dehydration. Deprotection of the pivaloyl group in 219 was then followed by coupling to a methacrylic group to afford a key intermediate, triene 220. This intermediate is now set up for the intramolecular Diels-Alder cycloaddition reaction, and upon heating in the presence of a radical scavenger (BHT), it afforded the tetracyclic lactone 221. Hydroboration-oxygenation of the internal alkene in 221 followed by a half reduction of the lactone 222 with DIBAL-H allowed access to the aldehyde 223, which was then converted into a secondary amine by reductive amination and protected with AllocCl to yield 224. This intermediate was then treated with DMP to afford a ketoaldehyde that was treated with Pd(PPh 3 ) 4 catalyst and acetic acid to remove the Alloc group and resulted in an intramolecular Mannich reaction. This sequence of manipulations provided the polycyclic system 225 and sets up the framework for the formation of the bicyclo[2.2.2] structural core. Two steps of functional group transformations accessed the ortho-quinone monoketal 226 that was treated with ethylene at 70 °C resulting in an intermolecular Diels-

Review Syn thesis
Alder reaction to give the bicyclo[2.2.2] 227; functional group manipulations and final deprotection of protecting groups gave lepenine (58). 51

Total Syntheses of Cochlearenine, N-Ethyl-1hydroxy-17-veratroyldictyzine, and Paniculamine
The Sarpong group embarked on the mammoth task to design a route that was suitably amenable to modifications at the latest possible stage and yet still access 59, 63, and 61/241; three denudatine-type diterpenoid alkaloids (Scheme 16). 52 This was achieved by designing a route to intermediate cochlearenine (59); from 59, following a few late-stage manipulations of the functional groups on the bicyclo[2.2.2] structural element, each of the intended targets was successfully accessed. Starting from 93, which the Sarpong group had previously designed and accessed in 10 steps (25% overall yield), 28 the primary alcohol was converted into the corresponding aldehyde 230 via a Swern oxidation. An aldol-Cannizzaro sequence on 230 afforded the diol 231, which was then converted into the dimesylate 102 (76%). Intermediate 102 was treated with KH to effect the cyclization yielding 232 as the sole product. Next, the methylene O-mesylate group of 232 was transformed into a methyl group via reduction with the combination of NaI/Zn. This was a key step in the strategy, as stereoselective installation of the methyl group, which is present in all the C 20 alkaloids, was achieved. Following the removal of the MOM protecting group, oxidative dearomatization of the resulting phenol afforded the dienone 233. This dienone was then heated to 150 °C to allow formation of the intramolecular Diels-Alder cycloaddition product 234, thus forming

Review Syn thesis
Scheme 17 Total synthesis of atisine-type diterpenoid alkaloids spiramilactone B, spiraminol, dihydroajaconine, spiramine C, and spiramine D The alkynyl-substituted ester 249 was desilylated and acylated, and then subjected to Ru-catalyzed cycloisomerization to give tetracyclic ketone 250 as a single diastereomeric product. To set up for the bridged core structure, intermediate 250 was treated with LiBEt 3 H, the C6-C7 olefin was epoxidized using m-CPBA, and the free hydroxyl group was protected; regioselective epoxide opening catalyzed by [Ti(Oi-Pr) 2 Cl 2 ] afforded the formation of hydroxy -lactone 251, thereby completing the pentacyclic core structure. This -lactone 251 was rearranged to the -lactone 252 over a few synthetic manipulations. Treatment of 252 with ozone gave the ketone which was converted into a terminal olefin by Takai olefination; 85 this lactone was then partially reduced to the aldolactol, followed by condensation with MeOH to afford 253. A hydroboration-oxidation reaction on the olefin of 253 allowed access to the primary alcohol, which was converted into the aldehyde, thus allowing for selective alkylation on treatment with potassium tert-butoxide and methyl iodide. The lactone 255 was directly accessed by a Pinnick oxidation 86

Review Syn thesis
core skeleton of spiramilactone B (259). At this point only a few tailoring steps were required to access the specific diterpenoids of the atisine type. 54

Radical-Based Cyclizations
In 2016, Inoue and co-workers disclosed the use of a radical-based cyclization/translocation/cyclization process followed by an aldol cyclization for the synthesis of the fused hexacycle of puberuline C (278) (Scheme 19). 88 Treatment of tricycle 272 with n-Bu 3 SnH and 273 (V-40) under refluxed conditions initiated a 7-endo cyclization from C11 to C10, followed by a 1,5-hydrogen abstraction from C7 to C17, and finally resulting in a transannular 6-exo cyclization from C17 to C8. The efficiency of this cascade is remarkable as five stereocenters (C8, C9, C10, C11, and C17) are introduced with the desired stereoconfiguration despite the moderate yield of 274 (54%). After treatment of 274

Review Syn thesis
with TBSOTf to give the silyl enol ether 275, variety of Lewis acids were screen for the intramolecular Mukaiyama aldol reaction of 275; this reaction was realized using SnCl 4 to activate the acetal moiety for the formation of the D ring in 277. The stereoconfiguration of C16 can be explained by the binding of SnCl 4 between the oxygen and nitrogen atoms in 276 which dictates the nucleophilic attack of the silyl enol ether on to the si-face of the oxocarbenium ion. Subsequent steps installed the stereocenter at C14 of the hexacyclic core of puberuline C.
In 2016, Inoue and co-workers detailed the formation of the pentacyclic core of talatisamine (49) via radical and cationic cyclizations (Scheme 20). 89 Treating 279 with n-Bu 3 SnH and 280 (V-70) resulted in the formation of a stereochemi-cally fixed C11 bridgehead radical 283 that underwent stereo-and regioselective 7-endo cyclization on to C10 to form the B ring in 284. Steric repulsion between the C5-TMS ether and C14-acetal moieties favored the transition state 283 over 281.
Purification of 284 with silica gel caused C14-oxygen elimination and C9 epimerization to form enone 285 and trans-fused 286 from the initial cis-fused 284, respectively. Treatment of 285 with NaH yields 286 in a 79% combined yield from 279. Pentacycle 286 was then converted into 287 in ten steps which were required to carry out a 6-endo cationic cyclization to install the D ring. The C15-C16 double bond was activated with PhSeCl, allowing attack by the TBS Scheme 19 Radical-based cyclization/translocation/cyclization process followed by an aldol reaction for the synthesis of the fused hexacycle of puberuline C

Review Syn thesis
enol ether to afford pentacycle 289. Finally, oxidation of selenide 289 triggers a selenoxide elimination to give the pentacyclic core 290 of talatisamine (49).
In 2017, Inoue and co-workers disclosed a three-component coupling approach to append the AE ring systems to the C ring of C 19 -diterpenoid alkaloids in an expedient manner (Scheme 21). 90 The strategy utilized a radical-polar crossover cascade initiated with Et 3 B/O 2 and iodide 291 to form a bridgehead radical that first underwent conjugate addition with enone 292 on the opposite side of the OTBS substituent. The boron enolate intermediate 293 then underwent an aldol addition with alkynal 294 via the sixmembered transition state 295 to form the coupled product 296. High chemoselectivity was demonstrated as no addition to the alkyne was observed. The simultaneous generation of three new stereocenters in a single step under mild reaction conditions proved to be an efficient method to provide the advanced intermediate for the synthesis of C 19 -diterpenoid alkaloids.
Scheme 21 Three-component radical-polar crossover cascade for the formation of the ACE ring systems of C 19 -diterpenoid alkaloids Wang, Xu, and co-workers utilized, in 2018, a 1,7-enyne reductive radical cyclization and double condensation for the synthesis of lycoctonine-type C 19 -norditerpenoid alkaloid (Scheme 22). 91 1,7-Enyne 297, which was prepared from a previously reported intermediate, 92 underwent a reductive cyclization to form the A ring of pentacyclic intermediate 298 when treated with n-Bu 3 SnH and AIBN. Double reductive amination of 299 with ethylamine followed by an acetonide removal furnished the hexacycle 300 which was the precursor to the pentacyclic core of methyllycaconitine (301).

Scheme 22 1,7-enyne reductive radical cyclization and double condensation for the synthesis of lycoctonine-type C 19 norditerpenoids
Another radical-based cyclization was adopted by Xu and co-workers in the synthesis of the BCD ring systems of 7,17-seco-type C 19 -norditerpenoid alkaloids (Scheme 23). 93 It was shown that similar ring systems can be accessed via a [3+2] cycloaddition of a nitrile oxide. Bicyclic iodide 304 participated in a radical cyclization when treated with n-Bu 3 SnH and AIBN to form tricyclic lactone 305 which can then be transformed into 306, a key intermediate to the ABEF ring system of C 19 -norditerpenoids. The alternative approach utilized an intramolecular [3+2] nitrile oxide cycloaddition to form the tricyclic system. Oxime 307 was oxidized into the nitrile oxide upon treatment with NCS, and this nitrile oxide underwent an intramolecular cycloaddition to form tricycle 308. Cleavage of the N-O bond was achieved under hydrogenolysis conditions with Raney nickel to afford -hydroxy ketone 309, which can then be transformed into the key tricyclic core 310.

Ruthenium-Mediated Enyne Cycloisomerization
Song, Qin, and co-workers drew inspiration from Trost's ruthenium-mediated enyne cycloisomerization 94 for the synthesis of the CD ring systems of aconitine (27) (Scheme 24). 95 Chiral enyne 311 was treated with 50 mol% Cp-Ru(MeCN) 3 PF 6 to give the five-membered ruthenacycle 312 which then underwent -hydride elimination followed by reductive elimination to give stereoisomers 313 and 314 in 2:3 ratio. Initial attempts were made with palladium catalysts, but they did not give cyclized products.

Review Syn thesis
Scheme 24 Ruthenium-mediated enyne cycloisomerization for the construction of CD ring systems of aconitine

Reductive Coupling
In 2014, Xu and co-workers reported the synthesis of ABEF ring systems of lycoctonine-type and 7,17-seco-type C 19 -norditerpenoid alkaloids starting from the trans-fused 6,7-bicycle 318 formed from a ruthenium-catalyzed diastereoselective enyne cycloisomerization protocol developed by Trost 94 (Scheme 25). 96 Treatment of bicycle 318 with m-CPBA in the presence of catalytic TsOH resulted in the stereoselective epoxidation of the olefin with concurrent ring-opening by the ester group to give tricyclic lactone 319. A series of transformations on 319 afforded tetracycle 320. Finally, reductive coupling between the ketone and N,O-acetal in 320 was accomplished using SmI 2 to form tetracycle 321 bearing the ABEF ring systems of Lycoctoninetype and 7,17-seco-type C 19 -norditerpenoid alkaloids.

Scheme 25
Construction of the ABEF ring system with rutheniumcatalyzed enyne cycloisomerization and SmI 2 -induced reductive coupling Sugita and co-workers reported a reductive cyclization strategy of ,-epoxy ketone 322 to synthesize the CD ring system of aconitine (27) (Scheme 26). 97 SmI 2 initiates the formation of samarium enolate 323 that subsequently underwent an intramolecular aldol cyclization with the pendant aldehyde. The reaction was expected to proceed through cyclic transition state 324. Initial reaction conditions either gave low yields of bicyclic ketone 325 or side products from premature protonation of 324 or with observed TES group migration. Optimized conditions with SmI 2 (6 equiv) and HMPA (24 equiv) furnished the desired product 327 in 71% yield.

Review Syn thesis
Scheme 26 Reductive cyclization of ,-epoxy ketone for the synthesis of CD ring systems of aconitine

Diels-Alder Reactions
Brimble and co-workers reported the enantioselective synthesis of the ABEF ring systems of methyllycaconitine analogues (Scheme 27). 98 The elegant approached utilized sequential Diels-Alder reaction, aldol, Mannich, and Wacker-type cyclizations to furnish the tetracyclic scaffold 337. The enantioselective synthesis commenced with a cobalt(III)-salen complex 331 catalyzed Diels-Alder reaction between enal 329 and diene 330 to give the endoadduct 332 in excellent yield and enantioselectivity; the benzyl group on the amine was necessary to affect high enantioselectivity. The endo-adduct 332 was then treated with LDA to promote intramolecular aldol cyclization between the ester and the aldehyde to give -hydroxy ester 333. A three-step sequence ending with an intramolecular Mannich reaction was used to construct the ABE tricyclic ring system 334. Reduction of the ketone in 334 gave alcohol 335, which underwent an intramolecular Wacker-type oxidative cyclization to install the F ring of the tetracycle 336. Subsequent transformations provided alcohol 337, representing the ABEF scaffold of methyllycaconitine analogues.
Xu, Wang, and co-workers initiated the synthesis of the AEF ring systems of C 19 -norditerpenoid alkaloids with a stereoselective intramolecular Diels-Alder reaction (Scheme 28). 99 The cycloadduct furnished the bicyclic lactone 341 with 5:1 endo selectivity thus establishing the A ring of the target. Subsequent transformations provided the N-protected aminoaldehyde 342. Deprotection of the Boc group in 342 under acidic conditions was followed by intramolecular Mannich reaction to furnish the tricyclic ketone 343, thus completing the synthesis of the AEF ring systems.

Scheme 28 Stereoselective Diels-Alder reaction and intramolecular
Mannich reaction for the synthesis of the AEF ring systems of C 19 -norditerpenoid alkaloids Barker and co-workers drew inspiration from the work of Yang and co-workers 100 by applying a tandem Diels-Alder/Mannich reaction for the construction of the AE and ABE ring systems of Delphinium alkaloids (Scheme 29). 101

Review Syn thesis
systems of Delphinium alkaloids. Similarly, using the dienecontaining a cyclohexene moiety 349 resulted in the formation of tricyclic ketone 350, which maps on to the ABE ring systems. Installation of the succinimide-bearing benzoyl group furnished the methyllycaconitine analogue 351. It was also shown that various derivatizations of the bicyclic core 347 could be used to give a wide variety of possible precursors of Delphinium and Aconitum alkaloids analogues

Oxidative Dearomatization/Diels-Alder Sequence
One of the extensively used strategies in syntheses of diterpenoid alkaloids and related diterpenes is the oxidative dearomatization/Diels-Alder cycloaddition cascade. 102 Xu, Wang, and co-workers also demonstrated the synthetic versatility of the Diels-Alder reaction by applying it to the synthesis of the BCD ring systems of C 19 -norditer-penoid alkaloids (Scheme 31). 92 An intramolecular Diels-Alder reaction of a masked o-benzoquinone 243 developed by Liao and co-workers was applied to synthesize the tetracyclic ketone 245. 82 PIDA-mediated oxidative dearomatization of phenol 242 in the presence of methanol gave diene 243 that underwent an intramolecular [4+2] cycloaddition to give 245. Subsequent transformations of 245 formed triflate 369, which underwent Wagner-Meerwein rearrangement, an alkyl shift with extrusion of the triflate group, in the presence of DBU and DMSO to form carbocation 370 that was trapped by DMSO giving 371. Elimination of dimethyl sulfide from 371 gave enone 372 thus constructing the BCD ring systems of C 19 -norditerpenoid alkaloids.
A similar PIDA-promoted oxidative cyclization strategy was applied by Xu, Wang, and co-workers to furnish the BCD ring systems of aconitine (27)

Review Syn thesis
Scheme 32 PIDA-promoted oxidative cyclization and a Wagner-Meerwein rearrangement to furnish the BCD rings systems of aconitine The Sarpong group presented studies in 2014 on C 20 -diterpenoid alkaloids, showing the synthesis of hetidine framework and its conversion into the atisine core structure. 104

Review Syn thesis
The versatile synthon 385 was used to synthesize compound 386 having the atisine carbon skeleton in 2 steps (Scheme 34). The same synthon was also used to synthesize dihydronavirine (387), which unfortunately could not be converted into the natural product navirine.
In a methodological study, Chen and Wang presented an efficient synthesis of the C/D rings (Scheme 35) of atisinetype C 20 -diterpenoid alkaloids. 105 The synthesis also relies on the oxidative dearomatization/intramolecular Diels-Alder strategy.

Scheme 35
Synthesis of the C/D rings of atisine-type C 20 -diterpenoid alkaloids Xu and co-workers accessed the core ring systems of Spiraea atisine-type diterpenoid alkaloids through a bio-inspired synthetic route. 106 A four-step process led from commercially available methyl cyclohex-1-enecarboxylate (391) to trans-decalin 392 (Scheme 36). Epoxidation of 392 in the presence of catalytic amounts of TsOH gave -lactone 393.

Transannular Aziridination
Xu and co-workers reported a PIDA-promoted intramolecular transannular aziridination strategy for the formation of the AEF ring systems of lycoctonine-type C 19 -nordi-terpenoid alkaloids (Scheme 37). 107 Starting from symmetric 397, intermediate 398 was obtained in 5 steps. -Keto acrylate 398 was subjected to TiCl 4 -mediated conjugate propargylation 108 followed by a gold(I)-catalyzed cyclization 109 to afford the -keto ester 400. Subsequent transformations of 400 furnished the amine 401 ready for intramolecular transannular aziridination. Initial conditions developed by Nagata and co-workers using lead(IV) acetate did not provide the desired product. 110 It was found that using PIDA together with silica gel as an additive gave the optimal yield of the aziridine 402. Finally, regioselective ring cleavage was achieved with ethyl iodide and DMF followed by treatment with NaOAc to give the tricyclic amine 403 that models the AEF ring systems of lycoctonine-type C 19 -norditerpenoid alkaloids.
Scheme 37 PIDA-promoted intramolecular transannular aziridination followed by regioselective ring cleavage to deliver the AEF ring systems of lycoctonine-type C 19

-norditerpenoid alkaloids
The racemulsonine family has been an evasive core in terms of successful attempts at its total synthesis. However, work by Wang and co-workers has made it significantly easier to access the 10-azatricyclo[3.3.2.0 4,8 ]decane skeleton precursor towards the final product (Scheme 38). 111 The strategy employed towards this synthesis of the cage-like azatricyclic skeleton was fashioned after the intramolecular aziridination reaction by Nagata and coworkers, 110

Review Syn thesis
protected and then converted into the -keto ester 405 in four steps. This diprotected diol 405 was then treated with DDQ, to provide the conjugated enone, 112 which underwent conjugate propargylation with allenyltriphenylstannane yielding 406. A Au(I)-catalyzed annulation via a modified Toste conditions 109 accessed the cis-fused cyclopentene scaffold 407 as a single diastereomer, thus completing the A/F ring core. Reduction of the ketone in 407 and protection with MeI installed the final C3-OMe group, and this was followed by deprotection of the benzyl protecting groups and monoprotection with TBSCl to afford the product as a mixture of the desired and undesired isomers (1.2:1); the alcohol was transformed into the primary amine 401. A modification of the method by Nagata and co-workers using 401 with PIDA and K 2 CO 3 in 1,2-dichloroethane at 55 °C gave the optimized yields of 402. The selective aziridine ring cleavage was then achieved by treatment of 402 with acetic anhydride, yielding the 10-azatricyclo[3.3.2.0 4,8 ]decane core (OAc analogue of 409) as a single regio-and stereoisomer in an excellent 90% yield. Notably, the direct introduction of the N-ethyl group to form the tricyclic amine was achieved by treatment of 402 with ethyl iodide followed by NaOAc to give N-ethyl tricyclic amine 403. 111 This work was expanded in 2016 113 by using exo-cyclization under radical conditions to furnish the B ring, thus expanding the scaffold. With just a few tailoring steps they were able to access 410 from compound 409, and cyclization occurred upon treatment of 410 with n-Bu 3 SnH and AIBN under reflux conditions in benzene to give 411 in 75% yield. At this stage, the ABEF core was completed, and with minor tailor-ing, the scaffold was further functionalized to give 412 which allows for further elaborations. This was an important development as this synthesis brought the work of Xu and co-workers much closer to the final racemulosine core.

Intramolecular [5+2] Cycloaddition
The synthesis of a 6/5/6/7 ring system (Scheme 39) matching parts of the skeleton of C 18 /C 19 -diterpenoid alkaloids was reported by Liu and co-workers in 2018. 114 The synthesis features an iron-catalyzed intramolecular [5+2] cycloaddition that they had reported earlier. 115 Cycloaddition adduct 415 was transformed into tetracyclic synthon 416 in 3 steps. It was also demonstrated that the chemoselective reduction of a ketone moiety is feasible. The result-

Review Syn thesis
ing synthon 417 features the A, B, and F rings and the precursor of the C/D ring system of the diterpenoid alkaloid skeletons.

Miscellaneous
The Sarpong group aimed to study the structural activity relationship of aconitine (27) and the variation of substituents on the D ring while maintaining the structure of the AEF ring systems (Scheme 40). 116 Starting with vinylnitrile 88, aryl nucleophiles with different substitution pattern were appended in a conjugate fashion under Hayashitype Rh-catalysis 117 or with the Cu-mediated strategy to give conjugate addition product 418. Subsequent elaborations on the products afforded tetracycle 419 or the dearomatized spirocycle 420.

Scheme 40
Conjugate arylation of vinylnitrile to study the structural activity relationship for aconitine An expedient synthesis of the AE ring systems bearing a 5-hydroxyl group for C 19 -norditerpenoid alkaloids was reported by Wang and co-workers utilizing a series of intramolecular Claisen condensation, double Mannich reaction, and stereoselective aldol addition (Scheme 41). 118 Starting with keto carbonate 422, Claisen condensation followed by methylation furnished the bicyclic -keto lactone 423. Double Mannich reaction with benzylamine in the presence of formaldehyde installed the E ring to give 424. Finally, stereoselective addition of a carbonyl group dictated by the 1substituent formed the 5-hydroxyl group in 425.

Conclusion
The diterpenoid alkaloids have proven to be an intriguing and challenging target to researchers worldwide. A century following their discovery, synthetic strategies towards diterpenoid alkaloids have continuously expanded. Herein, we summarized synthetic efforts over the past decade, dis-cussing successful total syntheses and pioneering work towards future attempts of total syntheses. The current success can be viewed as an open door towards accessing unnatural derivatives of these diterpenoid alkaloids in an effort to tune the prevalent biological activities.
Despite the great successes reported, there are still challenging targets left to synthesize, which is especially true for the C 19 -diterpenoid alkaloids with aconitine (27) as the most popular representative. Further, it can be expected that natural product isolation will yield additional structurally challenging compounds with interesting biological activities.

Funding Information
We thank the University of Toronto, and the Natural Sciences and Engineering Research Council (NSERC), and the Audrey and Ragnar Olsen Fellowship for financial support. Christian Dank was supported by an Erwin Schroedinger postdoctoral fellowship awarded by the Austrian Science Fund (FWF) J 4348-N28.A u s t r i a n S c i e n c e F u n d ( J 4 3 4 8 -N 2 8 )