Synlett 2017; 28(20): 2714-2754
DOI: 10.1055/s-0036-1590900
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© Georg Thieme Verlag Stuttgart · New York

Recent Synthetic Applications of Catalyst-Free Photochemistry

Wenbo Liu
Department of Chemistry and FQRNT Centre for Green Chemistry and Catalysis, McGill University, 801 Sherbrooke St. W., Montreal, Quebec H3A 0B8, Canada   Email: cj.li@mcgill.ca
,
Chao-Jun Li*
Department of Chemistry and FQRNT Centre for Green Chemistry and Catalysis, McGill University, 801 Sherbrooke St. W., Montreal, Quebec H3A 0B8, Canada   Email: cj.li@mcgill.ca
› Author Affiliations
We are grateful to the Canada Research Chair Foundation (to C.-J. Li), the CFI, FQRNT Center for Green Chemistry and Catalysis, NSERC, and McGill University for support of our research. W. Liu thanks McGill Chemistry for a Major Scholarship and CIHR for a Drug Development Training Program Scholarship.
Further Information

Publication History

Received: 18 June 2017

Accepted after revision: 07 August 2017

Publication Date:
14 September 2017 (online)


Dedicated to Professor Victor Snieckus on the occasion of his 80th birthday

Abstract

Catalyst-free photochemistry provides numerous opportunities toward sustainable synthesis because catalyst separation can usually be avoided, which is consistent with green chemistry principles. Complementary to the well-reviewed photoredox chemistry, this review specifically summarizes the synthetic applications of photochemistry without external catalysts reported since 2000. The selected examples include both natural product synthesis and new methodology development. This review is arranged based on the type of chromophore. It is our hope that this review will inspire more synthetic chemists to embrace photochemistry into their research plans.

1 Introduction

2 Photochemistry of Olefins

2.1 [2+2] Cycloaddition of Enones and Olefins

2.2 Cycloaddition of Olefins without Carbonyl Groups

2.3 Z/E Isomerization

2.4 Cyclization

2.5 Others

3 Photochemistry of C=O

3.1 The Paternò–Büchi Reaction

3.2 The Yang Photoenolization

3.3 The Norrish Type I Reaction

3.4 The Norrish Type II Reaction

3.5 Others

4 Photochemistry of Nitrogen-Containing Functional Groups

5 Photochemistry of Halogen-Containing Compounds

6 Conclusion and Outlook

 
  • References

    • 1a Ciamician G. Science 1912; 36: 385
    • 1b Roth HD. Angew. Chem. Int. Ed. 1989; 28: 1193
    • 1c Roth HD. Pure Appl. Chem. 2001; 73: 395
    • 2a Kärkäs MD. Porco JA. Stephenson CR. J. Chem. Rev. 2016; 116: 9683
    • 2b Hoffmann N. Chem. Rev. 2008; 108: 1052
    • 2c Bach T. Hehn JP. Angew. Chem. Int. Ed. 2011; 50: 1000
    • 2d Fagnoni M. Dondi D. Ravelli D. Albini A. Chem. Rev. 2007; 107: 2725
    • 2e Ravelli D. Protti S. Fagnoni M. Chem. Rev. 2016; 116: 9850
    • 2f Winkler JD. Bowen CM. Liotta F. Chem. Rev. 1995; 95: 2003
    • 2g Iriondo-Alberdi J. Greaney MF. Eur. J. Org. Chem. 2007; 4801
  • 3 Wender PA. Howbert JJ. J. Am. Chem. Soc. 1981; 103: 688
  • 4 Quinkert G. Weber W.-D. Schwartz U. Dürner G. Angew. Chem. Int. Ed. 1980; 19: 1027
    • 5a Zimmerman HE. Pure Appl. Chem. 2006; 78: 2193
    • 5b Turro NJ. Angew. Chem. Int. Ed. 1986; 25: 882
    • 5c Turro NJ. J. Org. Chem. 2011; 76: 9863
    • 6a Hartman RL. McMullen JP. Jensen KF. Angew. Chem. Int. Ed. 2011; 50: 7502
    • 6b Webb D. Jamison TF. Chem. Sci. 2010; 1: 675
    • 6c Wiles C. Watts P. Eur. J. Org. Chem. 2008; 1655
    • 6d Wiles C. Watts P. Green Chem. 2012; 14: 38
    • 6e Cambié D. Bottecchia C. Straathof NJ. W. Hessel V. Noël T. Chem. Rev. 2016; 116: 10276
  • 7 Hook BD. A. Dohle W. Hirst PR. Pickworth M. Berry MB. Booker-Milburn KI. J. Org. Chem. 2005; 70: 7558
    • 8a Romero NA. Nicewicz DA. Chem. Rev. 2016; 116: 10075
    • 8b Prier CK. Rankic DA. MacMillan DW. C. Chem. Rev. 2013; 113: 5322
    • 8c Tucker JW. Stephenson CR. J. J. Org. Chem. 2012; 77: 1617
    • 8d Yoon TP. Ischay MA. Du J. Nat. Chem. 2010; 2: 527
    • 8e Xuan J. Xiao W.-J. Angew. Chem. Int. Ed. 2012; 51: 6828
    • 8f Xi Y. Yi H. Lei A. Org. Biomol. Chem. 2013; 11: 2387
    • 8g Skubi KL. Blum TR. Yoon TP. Chem. Rev. 2016; 116: 10035
    • 8h Shaw MH. Twilton J. MacMillan DW. C. J. Org. Chem. 2016; 81: 6898
    • 9a Albini A. Fagnoni M. Green Chem. 2004; 6: 1
    • 9b Ravelli D. Dondi D. Fagnoni M. Albini A. Chem. Soc. Rev. 2009; 38: 1999
    • 9c Ravelli D. Fagnoni M. Albini A. Chem. Soc. Rev. 2013; 42: 97
    • 9d Li C.-J. Green Chem. 2016; 18: 1836
    • 9e Li C.-J. Chem 2016; 1: 423
    • 10a Mercer JA. M. Cohen CM. Shuken SR. Wagner AM. Smith MW. Moss FR. Smith MD. Vahala R. Gonzalez-Martinez A. Boxer SG. Burns NZ. J. Am. Chem. Soc. 2016; 138: 15845
    • 10b Sarkar N. Nayek A. Ghosh S. Org. Lett. 2004; 6: 1903
    • 10c Trecker DJ. Henry JP. McKeon JE. J. Am. Chem. Soc. 1965; 87: 3261
    • 10d Trecker DJ. Foote RS. Henry JP. McKeon JE. J. Am. Chem. Soc. 1966; 88: 3021
  • 11 Poplata S. Tröster A. Zou Y.-Q. Bach T. Chem. Rev. 2016; 116: 9748
  • 12 Schuster DI. Lem G. Kaprinidis NA. Chem. Rev. 1993; 93: 3
    • 13a Lee-Ruff E. Mladenova G. Chem. Rev. 2003; 103: 1449
    • 13b Bach T. Synthesis 1998; 683
    • 13c Gauvry N. Lescop C. Huet F. Eur. J. Org. Chem. 2006; 5207
  • 14 Namyslo JC. Kaufmann DE. Chem. Rev. 2003; 103: 1485
    • 15a Crimmins MT. Pace JM. Nantermet PG. Kim-Meade AS. Thomas JB. Watterson SH. Wagman AS. J. Am. Chem. Soc. 1999; 121: 10249
    • 15b Winkler JD. Doherty EM. J. Am. Chem. Soc. 1999; 121: 7425
    • 15c Crimmins MT. Pace JM. Nantermet PG. Kim-Meade AS. Thomas JB. Watterson SH. Wagman AS. J. Am. Chem. Soc. 2000; 122: 8453
  • 17 Hue BT. B. Dijkink J. Kuiper S. Larson KK. Guziec JF. S. Goubitz K. Fraanje J. Schenk H. van Maarseveen JH. Hiemstra H. Org. Biomol. Chem. 2003; 1: 4364
  • 18 Nielsen LB. Wege D. Org. Biomol. Chem. 2006; 4: 868
  • 19 de March P. Figueredo M. Font J. Raya J. Org. Lett. 2000; 2: 163
    • 20a Gauzy C. Pereira E. Faure S. Aitken DJ. Tetrahedron Lett. 2004; 45: 7095
    • 20b Aitken DJ. Gauzy C. Pereira E. Tetrahedron Lett. 2002; 43: 6177
    • 20c Gu X. Xian M. Roy-Faure S. Bolte J. Aitken DJ. Gefflaut T. Tetrahedron Lett. 2006; 47: 193
    • 20d Gauzy C. Saby B. Pereira E. Faure S. Aitken DJ. Synlett 2006; 1394
    • 21a Winkler JD. Rouse MB. Greaney MF. Harrison SJ. Jeon YT. J. Am. Chem. Soc. 2002; 124: 9726
    • 21b Winkler JD. Harrison SJ. Greaney MF. Rouse MB. Synthesis 2002; 2150
    • 22a Blaauw RH. Brière J.-F. de Jong R. Benningshof JC. J. van Ginkel AE. Fraanje J. Goubitz K. Schenk H. Rutjes FP. J. T. Hiemstra H. J. Org. Chem. 2001; 66: 233
    • 22b Brière J.-F. Blaauw RH. Benningshof JC. J. van Ginkel AE. van Maarseveen JH. Hiemstra H. Eur. J. Org. Chem. 2001; 2371
    • 22c Buu Hue BT. Dijkink J. Kuiper S. van Schaik S. van Maarseveen JH. Hiemstra H. Eur. J. Org. Chem. 2006; 127
    • 23a Faure S. Piva O. Tetrahedron Lett. 2001; 42: 255
    • 23b Faure S. Piva-Le-Blanc S. Bertrand C. Pete J.-P. Faure R. Piva O. J. Org. Chem. 2002; 67: 1061
  • 24 Morimoto T. Horiguchi T. Yamada K. Tsutsumi K. Kurosawa H. Kakiuchi K. Synthesis 2004; 753
    • 25a Alibés R. de March P. Figueredo M. Font J. Racamonde M. Parella T. Org. Lett. 2004; 6: 1449
    • 25b Pérez L. Alibés R. de March P. Busqué F. Figueredo M. Font J. J. Org. Chem. 2013; 78: 4483
    • 26a Lescop C. Mévellec L. Huet F. J. Org. Chem. 2001; 66: 4187
    • 26b Alibés R. Alvárez-Larena A. de March P. Figueredo M. Font J. Parella T. Rustullet A. Org. Lett. 2006; 8: 491
  • 27 Baran PS. Zografos AL. O’Malley DP. J. Am. Chem. Soc. 2004; 126: 3726
  • 28 Birman VB. Jiang X.-T. Org. Lett. 2004; 6: 2369
  • 29 Redon S. Piva O. Tetrahedron Lett. 2006; 47: 733
  • 30 Srikrishna A. Ramasastry SS. V. Tetrahedron Lett. 2005; 46: 7373
  • 31 Srikrishna A. Ramasastry SS. V. Tetrahedron Lett. 2006; 47: 335
  • 32 Mangion IK. MacMillan DW. C. J. Am. Chem. Soc. 2005; 127: 3696
  • 33 Bader SJ. Snapper ML. J. Am. Chem. Soc. 2005; 127: 1201
  • 34 Ng SM. Bader SJ. Snapper ML. J. Am. Chem. Soc. 2006; 128: 7315
  • 35 Ichikawa M. Aoyagi S. Kibayashi C. Tetrahedron Lett. 2005; 46: 2327
  • 36 Zhang F. Jia Y. Tetrahedron 2009; 65: 6840
  • 37 Meier R. Trauner D. Angew. Chem. Int. Ed. 2016; 55: 11251
  • 38 Shipe WD. Sorensen EJ. J. Am. Chem. Soc. 2006; 128: 7025
  • 39 Doroh B. Sulikowski GA. Org. Lett. 2006; 8: 903
  • 40 Inoue M. Sato T. Hirama M. J. Am. Chem. Soc. 2003; 125: 10772
  • 41 Mehta G. Singh SR. Angew. Chem. Int. Ed. 2006; 45: 953
  • 42 Inoue M. Sato T. Hirama M. Angew. Chem. Int. Ed. 2006; 45: 4843
  • 43 Shi L. Meyer K. Greaney MF. Angew. Chem. Int. Ed. 2010; 49: 9250
  • 44 Yamashita M. Yadav ND. Sawaki T. Takao I. Kawasaki I. Sugimoto Y. Miyatake A. Murai K. Takahara A. Kurume A. Ohta S. J. Org. Chem. 2007; 72: 5697
    • 46a Kemmler M. Bach T. Angew. Chem. Int. Ed. 2003; 42: 4824
    • 46b Kemmler M. Herdtweck E. Bach T. Eur. J. Org. Chem. 2004; 4582
    • 46c Basler B. Schuster O. Bach T. J. Org. Chem. 2005; 70: 9798
    • 48a Rau H. Chem. Rev. 1983; 83: 535
    • 48b Inoue Y. Chem. Rev. 1992; 92: 741
    • 48c Inoue Y. Wada T. Asaoka S. Sato H. Pete J.-P. Chem. Commun. 2000; 36: 251
    • 48d Griesbeck AG. Meierhenrich UJ. Angew. Chem. Int. Ed. 2002; 41: 3147
    • 48e Chen C. Chang V. Cai X. Duesler E. Mariano PS. J. Am. Chem. Soc. 2001; 123: 6433
    • 49a García-Expósito E. Álvarez-Larena Á. Branchadell V. Ortuño RM. J. Org. Chem. 2004; 69: 1120
    • 49b Tsutsumi K. Nakano H. Furutani A. Endou K. Merpuge A. Shintani T. Morimoto T. Kakiuchi K. J. Org. Chem. 2004; 69: 785
    • 49c Furutani A. Tsutsumi K. Nakano H. Morimoto T. Kakiuchi K. Tetrahedron Lett. 2004; 45: 7621
    • 49d Shintani T. Kusabiraki K. Hattori A. Furutani A. Tsutsumi K. Morimoto T. Kakiuchi K. Tetrahedron Lett. 2004; 45: 1849
    • 49e Tanaka K. Fujiwara T. Org. Lett. 2005; 7: 1501
  • 50 Leonelli F. Blesi F. Dirito P. Trombetta A. Ceccacci F. La Bella A. Migneco LM. Marini BettoloR. J. Org. Chem. 2011; 76: 6871
  • 51 Qian S. Zhao G. Chem. Commun. 2012; 48: 3530
  • 52 Lu P. Bach T. Angew. Chem. Int. Ed. 2012; 51: 1261
  • 53 Yang Y. Fu X. Chen J. Zhai H. Angew. Chem. Int. Ed. 2012; 51: 9825
  • 54 Fort DA. Woltering TJ. Nettekoven M. Knust H. Bach T. Angew. Chem. Int. Ed. 2012; 51: 10169
  • 55 Cherney EC. Green JC. Baran PS. Angew. Chem. Int. Ed. 2013; 52: 9019
  • 56 Maskill KG. Knowles JP. Elliott LD. Alder RW. Booker-Milburn KI. Angew. Chem. Int. Ed. 2013; 52: 1499
  • 57 Mayr F. Wiegand C. Bach T. Chem. Commun. 2014; 50: 3353
  • 58 Skiredj A. Beniddir MA. Joseph D. Leblanc K. Bernadat G. Evanno L. Poupon E. Angew. Chem. Int. Ed. 2014; 53: 6419
  • 59 Saya JM. Vos K. Kleinnijenhuis RA. van Maarseveen JH. Ingemann S. Hiemstra H. Org. Lett. 2015; 17: 3892
    • 60a White JD. Li Y. Kim J. Terinek M. J. Org. Chem. 2015; 80: 11806
    • 60b White JD. Li Y. Kim J. Terinek M. Org. Lett. 2013; 15: 882
  • 61 White JD. Ihle DC. Org. Lett. 2006; 8: 1081
  • 62 Ruider SA. Sandmeier T. Carreira EM. Angew. Chem. Int. Ed. 2015; 54: 2378
  • 63 Albertson AK. F. Lumb J.-P. Angew. Chem. Int. Ed. 2015; 54: 2204
  • 64 Kleinnijenhuis RA. Timmer BJ. J. Lutteke G. Smits JM. M. de Gelder R. van Maarseveen JH. Hiemstra H. Chem. Eur. J. 2016; 22: 1266
  • 65 Tanino K. Takahashi M. Tomata Y. Tokura H. Uehara T. Narabu T. Miyashita M. Nat. Chem. 2011; 3: 484
  • 66 Kurdyumov AV. Hsung RP. Ihlen K. Wang J. Org. Lett. 2003; 5: 3935
  • 67 Funaki T. Inokuma S. Ide H. Yonekura T. Nakamura Y. Nishimura J. Tetrahedron Lett. 2004; 45: 2393
  • 68 Inokuma S. Yatsuzuka T. Ohtsuki S. Hino S. Nishimura J. Tetrahedron 2007; 63: 5088
  • 69 Nie W.-L. Erker G. Kehr G. Fröhlich R. Angew. Chem. Int. Ed. 2004; 43: 310
  • 70 de Meijere A. Redlich S. Frank D. Magull J. Hofmeister A. Menzel H. König B. Svoboda J. Angew. Chem. Int. Ed. 2007; 46: 4574
  • 71 Holla H. Jenkins ID. Neve JE. Pouwer RH. Pham N. Teague SJ. Quinn RJ. Tetrahedron Lett. 2012; 53: 7101
  • 72 Zhang P. Wang Y. Bao R. Luo T. Yang Z. Tang Y. Org. Lett. 2012; 14: 162
  • 73 Hesse R. Gruner KK. Kataeva O. Schmidt AW. Knölker H.-J. Chem. Eur. J. 2013; 19: 14098
  • 74 Fukazawa A. Karasawa T. Zhang H. Minemura K. Camacho C. Wang J. Irle S. Yamaguchi S. Angew. Chem. Int. Ed. 2013; 52: 10519
  • 75 Williams DR. Nold AL. Mullins RJ. J. Org. Chem. 2004; 69: 5374
  • 76 Davies HM. L. Loe Ø. Stafford DG. Org. Lett. 2005; 7: 5561
  • 77 Moghaddam FM. Farimani MM. Tetrahedron Lett. 2010; 51: 540
  • 78 Hernandez-Perez AC. Vlassova A. Collins SK. Org. Lett. 2012; 14: 2988
  • 79 Toelle N. Weinstabl H. Gaich T. Mulzer J. Angew. Chem. Int. Ed. 2014; 53: 3859
  • 80 Sharma P. Griffiths N. Moses JE. Org. Lett. 2008; 10: 4025
  • 81 Bach T. Grosch B. Strassner T. Herdtweck E. J. Org. Chem. 2003; 68: 1107
  • 82 Scott LT. Boorum MM. McMahon BJ. Hagen S. Mack J. Blank J. Wegner H. de Meijere A. Science 2002; 295: 1500
  • 83 Yang M. Li J. Li A. Nat. Commun. 2015; 6: 6445
  • 84 Lu Z. Li Y. Deng J. Li A. Nat. Chem. 2013; 5: 679
    • 85a Shi Y. Yang B. Cai S. Gao S. Angew. Chem. Int. Ed. 2014; 53: 9539
    • 85b Cai S. Xiao Z. Ou J. Shi Y. Gao S. Org. Chem. Front. 2016; 3: 354
    • 86a Gao S. Wang Q. Huang LJ.-S. Lum L. Chen C. J. Am. Chem. Soc. 2010; 132: 371
    • 86b Gao S. Wang Q. Chen C. J. Am. Chem. Soc. 2009; 131: 1410
    • 87a Churruca F. Fousteris M. Ishikawa Y. von Wantoch Rekowski M. Hounsou C. Surrey T. Giannis A. Org. Lett. 2010; 12: 2096
    • 87b Pusch S. Schollmeyer D. Opatz T. Org. Lett. 2016; 18: 3043
  • 88 Gutekunst WR. Baran PS. J. Am. Chem. Soc. 2011; 133: 19076
  • 89 Limanto J. Snapper ML. J. Am. Chem. Soc. 2000; 122: 8071
  • 90 Williams MJ. Deak HL. Snapper ML. J. Am. Chem. Soc. 2007; 129: 486
    • 91a Wessig P. Czarnecki M. Badetko D. Schilde U. Kelling A. J. Org. Chem. 2016; 81: 9147
    • 91b Matsumoto S. Takase K. Ogura K. J. Org. Chem. 2008; 73: 1726
  • 92 Yang Z. Li Y. Pattenden G. Tetrahedron 2010; 66: 6546
  • 93 De Mayo P. Acc. Chem. Res. 1971; 4: 41
  • 94 Minter DE. Winslow CD. J. Org. Chem. 2004; 69: 1603
    • 95a Boyd JW. Greaves N. Kettle J. Russell AT. Steed JW. Angew. Chem. Int. Ed. 2005; 44: 944
    • 95b Penkett CS. Sims RO. French R. Dray L. Roome SJ. Hitchcock PB. Chem. Commun. 2004; 40: 1932
    • 95c Penkett CS. Byrne PW. Teobald BJ. Rola B. Ozanne A. Hitchcock PB. Tetrahedron 2004; 60: 2771
    • 95d Penkett CS. Sims RO. Byrne PW. Kingston L. French R. Dray L. Berritt S. Lai J. Avent AG. Hitchcock PB. Tetrahedron 2006; 62: 3423
    • 95e Vízvárdi K. Desmet K. Luyten I. Sandra P. Hoornaert G. Van der Eycken E. Org. Lett. 2001; 3: 1173
    • 95f Remy R. Bochet CG. Chem. Rev. 2016; 116: 9816
    • 95g Chu S. Münster N. Balan T. Smith MD. Angew. Chem. Int. Ed. 2016; 55: 14306
    • 95h Gaich T. Mulzer J. J. Am. Chem. Soc. 2009; 131: 452
    • 95i Gaich T. Mulzer J. Org. Lett. 2010; 12: 272
    • 95j Khatri BB. Vrubliauskas D. Sieburth SM. Tetrahedron Lett. 2015; 56: 4520
  • 96 Chu H. Smith JM. Felding J. Baran PS. ACS Cent. Sci. 2017; 3: 47
  • 97 Bos PH. Antalek MT. Porco JA. Stephenson CR. J. J. Am. Chem. Soc. 2013; 135: 17978
  • 98 Yang H. Feng J. Li Y. Tang Y. Org. Lett. 2015; 17: 1441
  • 99 Büchi G. Inman CG. Lipinsky ES. J. Am. Chem. Soc. 1954; 76: 4327
  • 100 Schreiber SL. Satake K. J. Am. Chem. Soc. 1984; 106: 4186
  • 101 Bach T. Brummerhop H. Harms K. Chem. Eur. J. 2000; 6: 3838
  • 102 Aungst RA. Jr. Funk RL. J. Am. Chem. Soc. 2001; 123: 9455
  • 103 Griesbeck AG. Bondock S. Lex J. J. Org. Chem. 2003; 68: 9899
  • 104 Boxall RJ. Ferris L. Grainger RS. Synlett 2004; 2379
  • 105 Iriondo-Alberdi J. Perea-Buceta JE. Greaney MF. Org. Lett. 2005; 7: 3969
  • 106 Yang NC. Rivas C. J. Am. Chem. Soc. 1961; 83: 2213
  • 107 Grosch B. Orlebar CN. Herdtweck E. Kaneda M. Wada T. Inoue Y. Bach T. Chem. Eur. J. 2004; 10: 2179
    • 108a Nicolaou KC. Gray D. Tae J. Angew. Chem. Int. Ed. 2001; 40: 3679
    • 108b Nicolaou KC. Gray DL. F. Tae J. J. Am. Chem. Soc. 2004; 126: 613
  • 109 Mejorado LH. Pettus TR. R. J. Am. Chem. Soc. 2006; 128: 15625
  • 110 Masuda Y. Ishida N. Murakami M. J. Am. Chem. Soc. 2015; 137: 14063
  • 111 Dell’Amico L. Fernández-Alvarez VM. Maseras F. Melchiorre P. Angew. Chem. Int. Ed. 2017; 56: 3304
  • 112 Dell’Amico L. Vega-Peñaloza A. Cuadros S. Melchiorre P. Angew. Chem. Int. Ed. 2016; 55: 3313
  • 113 Bamford CH. Norrish RG. W. J. Chem. Soc. 1935; 1504
  • 114 Ng D. Yang Z. Garcia-Garibay MA. Org. Lett. 2004; 6: 645
    • 115a Natarajan A. Ng D. Yang Z. Garcia-Garibay MA. Angew. Chem. Int. Ed. 2007; 46: 6485
    • 115b Hernández-Linares MG. Guerrero-Luna G. Pérez-Estrada S. Ellison M. Ortin M.-M. Garcia-Garibay MA. J. Am. Chem. Soc. 2015; 137: 1679
  • 116 Lainchbury MD. Medley MI. Taylor PM. Hirst P. Dohle W. Booker-Milburn KI. J. Org. Chem. 2008; 73: 6497
    • 117a Booker-Milburn KI. Anson CE. Clissold C. Costin NJ. Dainty RF. Murray M. Patel D. Sharpe A. Eur. J. Org. Chem. 2001; 1473
    • 117b Booker-Milburn KI. Hirst P. Charmant JP. H. Taylor LH. J. Angew. Chem. Int. Ed. 2003; 42: 1642
    • 117c Booker-Milburn KI. Dudin LF. Anson CE. Guile SD. Org. Lett. 2001; 3: 3005
    • 118a Ferrini S. Ponticelli F. Taddei M. J. Org. Chem. 2006; 71: 9217
    • 118b Guerrini G. Taddei M. Ponticelli F. J. Org. Chem. 2011; 76: 7597
    • 118c Magnus P. Lescop C. Tetrahedron Lett. 2001; 42: 7193
  • 119 Norrish RG. W. Bamford CH. Nature 1937; 140: 195
    • 120a Griesbeck AG. Heckroth H. J. Am. Chem. Soc. 2002; 124: 396
    • 120b Pedrosa R. Andrés C. Nieto J. del Pozo S. J. Org. Chem. 2005; 70: 1408
    • 120c Ota E. Mikame Y. Hirai G. Koshino H. Nishiyama S. Sodeoka M. Tetrahedron Lett. 2015; 56: 5991
    • 120d De Leon F. Kalagara S. Navarro AA. Mito S. Tetrahedron Lett. 2013; 54: 3147
    • 120e Moorthy JN. Mal P. Tetrahedron Lett. 2003; 44: 2493
  • 121 Wessig P. Mühling O. Angew. Chem. Int. Ed. 2001; 40: 1064
  • 122 Gerard B. Jones G. Porco JA. J. Am. Chem. Soc. 2004; 126: 13620
  • 123 Scully SS. Porco JA. Org. Lett. 2012; 14: 2646
  • 124 Hickford PJ. Baker JR. Bruce I. Booker-Milburn KI. Org. Lett. 2007; 9: 4681
  • 125 Majetich G. Yu J. Org. Lett. 2008; 10: 89
  • 126 Álvarez-Dorta D. León EI. Kennedy AR. Riesco-Fagundo C. Suárez E. Angew. Chem. Int. Ed. 2008; 47: 8917
  • 127 Renata H. Zhou Q. Baran PS. Science 2013; 339: 59
  • 128 Renata H. Zhou Q. Dünstl G. Felding J. Merchant RR. Yeh C.-H. Baran PS. J. Am. Chem. Soc. 2015; 137: 1330
  • 129 Liu W. Chen N. Yang X. Li L. Li C.-J. Chem. Commun. 2016; 52: 13120
  • 130 Ito K. Tamashima H. Iwasawa N. Kusama H. J. Am. Chem. Soc. 2011; 133: 3716
  • 131 Becker P. Priebbenow DL. Pirwerdjan R. Bolm C. Angew. Chem. Int. Ed. 2014; 53: 269
  • 132 Becker P. Priebbenow DL. Zhang H.-J. Pirwerdjan R. Bolm C. J. Org. Chem. 2014; 79: 814
  • 133 Li L. Mu X. Liu W. Wang Y. Mi Z. Li C.-J. J. Am. Chem. Soc. 2016; 138: 5809
  • 134 Buscemi S. Pace A. Calabrese R. Vivona N. Metrangolo P. Tetrahedron 2001; 57: 5865
  • 135 Mascitti V. Corey EJ. J. Am. Chem. Soc. 2004; 126: 15664
  • 136 Mascitti V. Corey EJ. J. Am. Chem. Soc. 2006; 128: 3118
  • 137 Alonso R. Campos PJ. García B. Rodríguez MA. Org. Lett. 2006; 8: 3521
  • 138 McBurney RT. Slawin AM. Z. Smart LA. Yu Y. Walton JC. Chem. Commun. 2011; 47: 7974
    • 139a Paquette LA. Barton WR. S. Gallucci JC. Org. Lett. 2004; 6: 1313
    • 139b Paquette LA. Dura RD. Fosnaugh N. Stepanian M. J. Org. Chem. 2006; 71: 8438
  • 140 Chen K. Richter JM. Baran PS. J. Am. Chem. Soc. 2008; 130: 7247
  • 141 Wolff ME. Chem. Rev. 1963; 63: 55
  • 142 Chen K. Baran PS. Nature 2009; 459: 824
  • 143 Vaske YS. M. Mahoney ME. Konopelski JP. Rogow DL. McDonald WJ. J. Am. Chem. Soc. 2010; 132: 11379
  • 144 Deng J. Li R. Luo Y. Li J. Zhou S. Li Y. Hu J. Li A. Org. Lett. 2013; 15: 2022
  • 145 Hu P. Snyder SA. J. Am. Chem. Soc. 2017; 139: 5007
  • 146 Chapman LM. Beck JC. Wu L. Reisman SE. J. Am. Chem. Soc. 2016; 138: 9803
  • 147 Shi Z. Ren Y. Li B. Lu S. Zhang W. Chem. Commun. 2010; 46: 3973
  • 148 de Loera D. Garcia-Garibay MA. Org. Lett. 2012; 14: 3874
  • 149 Ren Y.-w. Wang X. Wang W. Li B. Shi Z.-j. Zhang W. Tetrahedron Lett. 2011; 52: 192
  • 150 Kan C. Long CM. Paul M. Ring CM. Tully SE. Rojas CM. Org. Lett. 2001; 3: 381
  • 151 Sato S. Yamada M. Wakahara T. Tsuchiya T. Ishitsuka MO. Akasaka T. Liu MT. H. Tetrahedron Lett. 2007; 48: 6290
  • 152 Xu W. Wu S. Zhou L. Liang G. Org. Lett. 2013; 15: 1978
    • 153a Shiraki S. Vogelsberg CS. Garcia-Garibay MA. Photochem. Photobiol. Sci. 2012; 11: 1929
    • 153b de Loera D. Stopin A. Garcia-Garibay MA. J. Am. Chem. Soc. 2013; 135: 6626
    • 153c Chung TS. Lopez SA. Houk KN. Garcia-Garibay MA. Org. Lett. 2015; 17: 4568
    • 153d Wang Y. Hu WJ. Song W. Lim RK. V. Lin Q. Org. Lett. 2008; 10: 3725
  • 154 Drouin A. Winter DK. Pichette S. Aubert-Nicol S. Lessard J. Spino C. J. Org. Chem. 2011; 76: 164
  • 155 Smith BT. Wendt JA. Aubé J. Org. Lett. 2002; 4: 2577
  • 156 Bhuvan Kumar NN. Kuznetsov DM. Kutateladze AG. Org. Lett. 2015; 17: 438
    • 157a Mukhina OA. Kumar NN. B. Cowger TM. Kutateladze AG. J. Org. Chem. 2014; 79: 10956
    • 157b Cronk WC. Mukhina OA. Kutateladze AG. J. Org. Chem. 2014; 79: 1235
    • 157c Mukhina OA. Bhuvan Kumar NN. Arisco TM. Valiulin RA. Metzel GA. Kutateladze AG. Angew. Chem. Int. Ed. 2011; 50: 9423
    • 157d Kumar NN. B. Mukhina OA. Kutateladze AG. J. Am. Chem. Soc. 2013; 135: 9608
    • 158a Zhang Y. Wang L. Zhang M. Fun H.-K. Xu J.-H. Org. Lett. 2004; 6: 4893
    • 158b Zhu M. Qiu Z. Hiel GP. Sieburth SM. J. Org. Chem. 2002; 67: 3487
    • 158c Sieburth SM. Madsen-Duggan CB. Zhang F. Tetrahedron Lett. 2001; 42: 5155
    • 158d Sieburth SM. McGee KF. Zhang F. Chen Y. J. Org. Chem. 2000; 65: 1972
    • 158e Lee Y.-g. McGee KF. Chen J. Rucando D. Sieburth SM. J. Org. Chem. 2000; 65: 6676
    • 158f McGee KF. Al-Tel TH. Sieburth SM. N. Synthesis 2001; 1185
    • 158g Lim Y.-H. Li T. Chen P. Schreiber P. Kuznetsova L. Carroll PJ. Lauher JW. Sieburth SM. Org. Lett. 2005; 7: 5413
    • 158h Song D. McDonald R. West FG. Org. Lett. 2006; 8: 4075
    • 158i Kulyk S. Khatri BB. Sieburth SM. Org. Lett. 2014; 16: 4138
  • 159 Garbarino S. Protti S. Basso A. Synthesis 2015; 47: 2385
  • 160 Southgate EH. Pospech J. Fu J. Holycross DR. Sarlah D. Nat. Chem. 2016; 8: 922
  • 161 Okumura M. Nakamata Huynh SM. Pospech J. Sarlah D. Angew. Chem. Int. Ed. 2016; 55: 15910
  • 162 Liu W. Yang X. Zhou Z.-Z. Li C.-J. Chem 2017; 2: 688
    • 163a Ouchi A. Hyugano T. Liu C. Org. Lett. 2009; 11: 4870
    • 163b Conner ES. Crocker KE. Fernando RG. Fronczek FR. Stanley GG. Ragains JR. Org. Lett. 2013; 15: 5558
    • 163c Cheng Y. Yang J. Qu Y. Li P. Org. Lett. 2012; 14: 98
  • 164 Li J. Jeong S. Esser L. Harran PG. Angew. Chem. Int. Ed. 2001; 40: 4765
  • 165 Bajtos B. Pagenkopf BL. Eur. J. Org. Chem. 2009; 1072
  • 166 Guizzardi B. Mella M. Fagnoni M. Albini A. Chem. Eur. J. 2003; 9: 1549
    • 167a Fraboni A. Fagnoni M. Albini A. J. Org. Chem. 2003; 68: 4886
    • 167b Freccero M. Fagnoni M. Albini A. J. Am. Chem. Soc. 2003; 125: 13182
    • 167c Protti S. Fagnoni M. Mella M. Albini A. J. Org. Chem. 2004; 69: 3465
    • 167d Mella M. Fagnoni M. Albini A. Org. Biomol. Chem. 2004; 2: 3490
    • 167e Protti S. Fagnoni M. Albini A. Org. Biomol. Chem. 2005; 3: 2868
    • 167f Fagnoni M. Albini A. Acc. Chem. Res. 2005; 38: 713
    • 167g Dichiarante V. Fagnoni M. Mella M. Albini A. Chem. Eur. J. 2006; 12: 3905
    • 167h Dichiarante V. Fagnoni M. Albini A. Angew. Chem. Int. Ed. 2007; 46: 6495
    • 167i Lazzaroni S. Dondi D. Fagnoni M. Albini A. Eur. J. Org. Chem. 2007; 4360
    • 167j Lazzaroni S. Protti S. Fagnoni M. Albini A. Org. Lett. 2009; 11: 349
    • 167k Raviola C. Canevari V. Protti S. Albini A. Fagnoni M. Green Chem. 2013; 15: 2704
    • 167l Qrareya H. Raviola C. Protti S. Fagnoni M. Albini A. J. Org. Chem. 2013; 78: 6016
  • 168 De Carolis M. Protti S. Fagnoni M. Albini A. Angew. Chem. Int. Ed. 2005; 44: 1232
  • 169 Protti S. Fagnoni M. Albini A. Angew. Chem. Int. Ed. 2005; 44: 5675
  • 170 Dichiarante V. Fagnoni M. Albini A. Chem. Commun. 2006; 42: 3001
  • 171 Protti S. Fagnoni M. Albini A. J. Am. Chem. Soc. 2006; 128: 10670
  • 172 Protti S. Dondi D. Fagnoni M. Albini A. Eur. J. Org. Chem. 2008; 2240
  • 173 Barolo SM. Teng X. Cuny GD. Rossi RA. J. Org. Chem. 2006; 71: 8493
    • 174a Vaillard VA. Budén ME. Martín SE. Rossi RA. Tetrahedron Lett. 2009; 50: 3829
    • 174b Peisino LE. Camargo Solorzano GP. Buden ME. Pierini AB. RSC Adv. 2015; 5: 36374
    • 174c Budén ME. Rossi RA. Tetrahedron Lett. 2007; 48: 8739
    • 174d Budén ME. Guastavino JF. Rossi RA. Org. Lett. 2013; 15: 1174
    • 175a Linsenmeier AM. Williams CM. Bräse S. J. Org. Chem. 2011; 76: 9127
    • 175b Linsenmeier AM. Williams CM. Bräse S. Eur. J. Org. Chem. 2013; 3847
  • 176 Budén ME. Dorn VB. Gamba M. Pierini AB. Rossi RA. J. Org. Chem. 2010; 75: 2206
  • 177 Li F. Castle SL. Org. Lett. 2007; 9: 4033
  • 178 Li F. Tartakoff SS. Castle SL. J. Am. Chem. Soc. 2009; 131: 6674
    • 179a Sudo Y. Yamaguchi E. Itoh A. Org. Lett. 2017; 19: 1610
    • 179b Yamaguchi T. Yamaguchi E. Itoh A. Org. Lett. 2017; 19: 1282
  • 180 Shi J. Manolikakes G. Yeh C.-H. Guerrero CA. Shenvi RA. Shigehisa H. Baran PS. J. Am. Chem. Soc. 2011; 133: 8014
  • 181 Zou Y. Deiters A. J. Org. Chem. 2010; 75: 5355
  • 182 Sonogashira K. Tohda Y. Hagihara N. Tetrahedron Lett. 1975; 16: 4467
  • 183 Protti S. Fagnoni M. Albini A. J. Org. Chem. 2012; 77: 6473
    • 184a Arceo E. Jurberg ID. Álvarez-Fernández A. Melchiorre P. Nat. Chem. 2013; 5: 750
    • 184b Woźniak Ł. Murphy JJ. Melchiorre P. J. Am. Chem. Soc. 2015; 137: 5678
    • 184c Bahamonde A. Melchiorre P. J. Am. Chem. Soc. 2016; 138: 8019
    • 184d Filippini G. Silvi M. Melchiorre P. Angew. Chem. Int. Ed. 2017; 56: 4447
    • 184e Arceo E. Bahamonde A. Bergonzini G. Melchiorre P. Chem. Sci. 2014; 5: 2438
  • 185 Silvi M. Verrier C. Rey YP. Buzzetti L. Melchiorre P. Nat. Chem. 2017; 9: 868
  • 186 Filippini G. Nappi M. Melchiorre P. Tetrahedron 2015; 71: 4535
  • 187 Liu W. Li L. Li C.-J. Nat. Commun. 2015; 6: 6526
  • 188 Liu W. Li L. Chen Z. Li C.-J. Org. Biomol. Chem. 2015; 13: 6170
    • 189a Liu W. Chen Z. Li L. Wang H. Li C.-J. Chem. Eur. J. 2016; 22: 5888
    • 189b Zhang Y. An Y. Sun J. Ding A. Wang Y. Rios R. Guo H. Tetrahedron Lett. 2015; 56: 6499
    • 189c Tsuchii K. Ogawa A. Tetrahedron Lett. 2003; 44: 8777
  • 190 Liu W. Li C.-J. Tetrahedron Lett. 2015; 56: 1699
  • 191 Itsenko O. Kihlberg T. Långström B. J. Org. Chem. 2004; 69: 4356
  • 192 Bian J. Van Wingerden M. Ready JM. J. Am. Chem. Soc. 2006; 128: 7428
    • 193a Nobuta T. Hirashima S.-i. Tada N. Miura T. Itoh A. Org. Lett. 2011; 13: 2576
    • 193b Kanai N. Nakayama H. Tada N. Itoh A. Org. Lett. 2010; 12: 1948
    • 193c Usami K. Nagasawa Y. Yamaguchi E. Tada N. Itoh A. Org. Lett. 2016; 18: 8
    • 194a Li L. Liu W. Mu X. Mi Z. Li C.-J. Nat. Protoc. 2016; 11: 1948
    • 194b Li L. Liu W. Zeng H. Mu X. Cosa G. Mi Z. Li C.-J. J. Am. Chem. Soc. 2015; 137: 8328
  • 195 Yang X. Liu W. Li L. Wei W. Li C.-J. Chem. Eur. J. 2016; 22: 15252
  • 196 Liu W. Yang X. Gao Y. Li C.-J. J. Am. Chem. Soc. 2017; 139: 8621
  • 197 Mfuh AM. Doyle JD. Chhetri B. Arman HD. Larionov OV. J. Am. Chem. Soc. 2016; 138: 2985
    • 198a Chen K. Zhang S. He P. Li P. Chem. Sci. 2016; 7: 3676
    • 198b Chen K. Cheung MS. Lin Z. Li P. Org. Chem. Front. 2016; 3: 875
  • 199 Mfuh AM. Nguyen VT. Chhetri B. Burch JE. Doyle JD. Nesterov VN. Arman HD. Larionov OV. J. Am. Chem. Soc. 2016; 138: 8408
  • 200 Chen K. He P. Zhang S. Li P. Chem. Commun. 2016; 52: 9125
  • 201 An Y. Kuang Y. Wu J. Org. Chem. Front. 2016; 3: 994
  • 202 Xiang Y. Kuang Y. Wu J. Org. Chem. Front. 2016; 3: 901
  • 203 An Y. Li Y. Wu J. Org. Chem. Front. 2016; 3: 570
  • 204 Zhou K. Xia H. Wu J. Org. Chem. Front. 2016; 3: 865
  • 205 Hung K. Condakes ML. Morikawa T. Maimone TJ. J. Am. Chem. Soc. 2016; 138: 16616
  • 206 Yang H.-T. Ren W.-L. Dong C.-P. Yang Y. Sun X.-Q. Miao C.-B. Tetrahedron Lett. 2013; 54: 6799