DOI: 10.1055/s-00000083

Synlett

Ausgabe 10 · Volume 27 · Juni 2016 DOI: 10.1055/s-006-31847

synpacts

  • 1443
    Ting, Chi P.; Maimone, Thomas J.:

    The Total Synthesis of Hyperforin

    Image for article: The Total Synthesis of Hyperforin
  • 1450
    Liu, Liu; Wang, Qing; Zhu, Ranran; Huang, Jianhui:

    A Massé Shot: Transition-Metal-Catalyzed Selective meta-C–H Functionalization (ortho-Metallation and para-Bromination Relay)

    Image for article: A Massé Shot: Transition-Metal-Catalyzed Selective <i>meta</i>-C–H Functionalization (<i>ortho</i>-Metallation and <i>para</i>-Bromination Relay)

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  • 1456
    Aradi, Klára; Tóth, Balázs L.; Tolnai, Gergely L.; Novák, Zoltán:

    Diaryliodonium Salts in Organic Syntheses: A Useful Compound Class for Novel Arylation Strategies

    Image for article: Diaryliodonium Salts in Organic Syntheses: A Useful Compound Class for Novel Arylation Strategies
  • 1486
    Dolfen, Jeroen; De Kimpe, Norbert; D’hooghe, Matthias:

    Deployment of Small-Ring Azaheterocycles as Building Blocks for the Synthesis of Organofluorine Compounds

    Image for article: Deployment of Small-Ring Azaheterocycles as Building Blocks for the Synthesis of Organofluorine Compounds

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  • 1511
    Zolfigol, Mohammad Ali; Mansouri, Navid; Baghery, Saeed:

    Synthesis of [2,2′-Bipyridine]-1,1′-diium Tricyanomethanide as a Bifunctional Nanostructured Ionic Liquid: Application to the Synthesis of 2-Aryl-5-methyl-2,3-dihydro-1H-3-pyrazolone Derivatives

    Image for article: Synthesis of [2,2′-Bipyridine]-1,1′-diium Tricyanomethanide as a Bifunctional Nanostructured Ionic Liquid: Application to the Synthesis of 2-Aryl-5-methyl-2,3-dihydro-1<i>H</i>-3-pyrazolone Derivatives
    Supporting Information (PDF)
  • 1516
    Lindsay-Scott, Peter J.; Barlow, Helen:

    Utilizing Solubility Differences to Achieve Regiocontrol in the Synthesis of Substituted Quinoline-4-carboxylic Acids

    Image for article: Utilizing Solubility Differences to Achieve Regiocontrol in the Synthesis of Substituted Quinoline-4-carboxylic Acids
    Supporting Information (PDF)
  • 1521
    Jung, Sunna; Kitajima, Yoko; Ueda, Yasuyuki; Suzuki, Keisuke; Ohmori, Ken:

    Stereocontrolled Synthesis of Planar Chiral Carba-Paracyclophanes via Modular Assembly

    Image for article: Stereocontrolled Synthesis of Planar Chiral Carba-Paracyclophanes via Modular Assembly
    Supporting Information (PDF)
  • 1527
    Manikandan, Chitrarasu; Ganesan, Kilivelu:

    Solid-Supported Synthesis of Flexible Dimeric Pyridinium Salts and Their Catalytic Activities

    Image for article: Solid-Supported Synthesis of Flexible Dimeric Pyridinium Salts and Their Catalytic Activities
    Supporting Information (PDF)
  • 1531
    Junk, Lukas; Kazmaier, Uli:

    A Straightforward Protocol for the Synthesis of Functionalized Tryptophan Peptides via Stille Coupling, Azidation and Photoinduced Nitrene Insertion

    Image for article: A Straightforward Protocol for the Synthesis of Functionalized Tryptophan Peptides <i>via</i> Stille Coupling, Azidation and Photoinduced Nitrene Insertion
    Supporting Information (PDF)
  • 1537
    Kaboudin, Babak; Haghighat, Hamideh; Yokomatsu, Tsutomu:

    Studies on the Synthesis of Novel Four-Membered Cyclic Oxaphosphetanes via Intramolecular Mitsunobu Reaction of Bishydroxyalkylphosphinic Acids

    Image for article: Studies on the Synthesis of Novel Four-Membered Cyclic Oxaphosphetanes via Intramolecular Mitsunobu Reaction of Bishydroxyalkylphosphinic Acids
    Supporting Information (PDF)
  • 1541
    Pieterse, Tanya; Visser, Melanie; Marais, Charlene; Bezuidenhoudt, Barend C. B.:

    Al(OTf)3: An Efficient Lewis Acid Additive for Domino Addition–Elimination of Grignard Reagents to Activated Ketones

    Image for article: Al(OTf)<sub>3</sub>: An Efficient Lewis Acid Additive for Domino Addition–Elimination of Grignard Reagents to Activated Ketones
    Supporting Information (PDF)
  • 1547
    Khoumeri, Omar; Vanelle, François-Xavier; Crozet, Maxime D.; Terme, Thierry; Vanelle, Patrice:

    Rapid and Convenient Synthesis of Original 5-Substituted Quinolino[3,4-b]quinoxalin-6(5H)-ones under Eco-Friendly Conditions

    Image for article: Rapid and Convenient Synthesis of Original 5-Substituted Quinolino[3,4-<i>b</i>]quinoxalin-6(5<i>H</i>)-ones under Eco-Friendly Conditions
    Supporting Information (PDF)
  • 1551
    Gayral, Maud; Frlan, Rok; Mravljak, Janez; Gravier-Pelletier, Christine:

    Nucleophilic Opening of an Epoxide by a Masked Glycine Anion Equivalent: A Route to C-Glycosyl Amino Acids

    Image for article: Nucleophilic Opening of an Epoxide by a Masked Glycine Anion Equivalent: A Route to <i>C</i>-Glycosyl Amino Acids
  • 1557
    Hsieh, Ping-An; Badsara, Satpal Singh; Tsai, Chia-Hsuan; Reddy, Daggula Mallikarjuna; Lee, Chin-Fa:

    Peracetic Acid Mediated sp2 C–H Selenation of Arenes

    Image for article: Peracetic Acid Mediated sp<sup>2</sup> C–H Selenation of Arenes
    Supporting Information (PDF)
  • 1563
    Zhang, Xu; Liu, Wenmin; Sun, Ruixue; Xu, Xuefeng; Wang, Zhiqiang; Yan, Yanlei:

    Silver-Catalyzed Three-Component Approach to Quinolines Starting from Anilines, Aldehydes, and Alcohols

    Image for article: Silver-Catalyzed Three-Component Approach to Quinolines Starting from Anilines, Aldehydes, and Alcohols
    Supporting Information (PDF)
  • 1569
    Stroganova, Tatyana A.; Vasilin, Vladimir K.; Krapivin, Gennady D.:

    Transformations of 3-Amino-N-[2-(5-methyl-2-furyl)ethyl]thieno[2,3-b]pyridine-2-carboxamides in Acidic Media

    Image for article: Transformations of 3-Amino-<i>N</i>-[2-(5-methyl-2-furyl)ethyl]thieno[2,3-<i>b</i>]pyridine-2-carboxamides in Acidic Media
    Supporting Information (PDF)
  • 1572
    Kerim, Mansour Dolè; El Kaïm, Laurent:

    Piperazine as Leaving Group in A3 Adducts: Fast Access to Alkynyl Indoles

    Image for article: Piperazine as Leaving Group in A3 Adducts: Fast Access to Alkynyl Indoles
    Supporting Information (PDF)
  • 1577
    Moon, Hyun Kyung; Sung, Gi Hyeon; Yoon, Yong-Jin; Yoon, Hyo Jae:

    Alkyl and Aryl 4,5-Dichloro-6-oxopyridazin-1(6H)-carboxylates: A Practical Alternative to Chloroformates for the Synthesis of Symmetric and Asymmetric Carbonates

    Image for article: Alkyl and Aryl 4,5-Dichloro-6-oxopyridazin-1(6<i>H</i>)-carboxylates: A Practical Alternative to Chloroformates for the Synthesis of Symmetric and Asymmetric Carbonates
    Supporting Information (PDF)
  • 1582
    Sasaki, Ikuo; Ikeda, Toshiki; Amou, Tatsunosuke; Taguchi, Jumpei; Ito, Hajime; Ishiyama, Tatsuo:

    Regioselective C–H Borylation of Heteroaromatic Aldimines with Iridium Complexes

    Image for article: Regioselective C–H Borylation of Heteroaromatic Aldimines with Iridium Complexes
    Supporting Information (PDF)
  • 1587
    Zhang, Jifa; Zhang, Jianqiao; Kang, Yulong; Shi, Jiangong; Yao, Chunsuo:

    A Facile and Practical Total Synthetic Route for Ampelopsin F and Permethylated ε-Viniferin

    Image for article: A Facile and Practical Total Synthetic Route for Ampelopsin F and Permethylated ε-Viniferin
    Supporting Information (PDF)
  • 1592
    Chang, Hong-Hong; Hu, Fei; Gao, Wen-Chao; Liu, Tao; Li, Xing; Wei, Wen-Long; Qiao, Yan:

    Iodine-Mediated Oxidative Dehydrogenation of β-Acylamino Ketones for the Highly Stereoselective Synthesis of (Z)-β-Keto­enamides

    Image for article: Iodine-Mediated Oxidative Dehydrogenation of β-Acylamino Ketones for the Highly Stereoselective Synthesis of (<i>Z</i>)-β-Keto­enamides
    Supporting Information (PDF)
  • 1597
    Li, Ning; Li, Baoguo; Chen, Shufeng:

    Base-Promoted Ecofriendly Synthesis of Trisubstituted Pyrazoles from α,β-Alkynyl N-Tosylhydrazones under Metal- and Solvent-Free Conditions

    Image for article: Base-Promoted Ecofriendly Synthesis of Trisubstituted Pyrazoles from α,β-Alkynyl <i>N</i>-Tosylhydrazones under Metal- and Solvent-Free Conditions
    Supporting Information (PDF)
  • 1602
    Wang, Leifeng; Yan, Zhiming:

    Visible-Light-Mediated Facile Reductive Aromatization of Quinols

    Image for article: Visible-Light-Mediated Facile Reductive Aromatization of Quinols
    Supporting Information (PDF)