Enantioselective Total Synthesis of (-)-Limaspermidine and (-)-Kopsinine by a Nitroaryl Transfer Cascade Strategy

被引:15
作者
Horst, Brendan [1 ]
Verdoorn, Daniel S. [1 ]
Hennig, Sven [1 ]
van der Heijden, Gydo [1 ]
Ruijter, Eelco [1 ]
机构
[1] Amsterdam Inst Mol & Life Sci AIMMS, Dept Chem & Pharmaceut Sci, De Boelelaan 1108, NL-1081 HZ Amsterdam, Netherlands
基金
荷兰研究理事会;
关键词
Alkaloids; Asymmetric Synthesis; Domino Reactions; Total Synthesis; CONCISE TOTAL SYNTHESES; ASPIDOSPERMA ALKALOIDS; NATURAL-PRODUCTS; INDOLE ALKALOIDS; FORMAL SYNTHESIS; PALLADIUM; ORGANOCASCADE; ALKYLATION;
D O I
10.1002/anie.202210592
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report an intramolecular conjugate addition/Truce-Smiles/Elcb cascade of 2-nitrobenzenesulfonamide-functionalized cyclohexenones as a new entry to the core scaffold of monoterpene indole alkaloids. The method was applied to the asymmetric total synthesis of (-)-limaspermidine, (-)-kopsinilam, and (-)-kopsinine, as well as the framework of the kopsifoline alkaloids, thus highlighting its complementarity to existing approaches involving the use of indole-based starting materials or the interrupted Fischer indole synthesis. Furthermore, we show that the cascade tolerates various substituents on the nitroarene, opening the way to other natural products as well as non-natural analogues.
引用
收藏
页数:5
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共 62 条
  • [1] Total Synthesis of (+)-Scholarisine A
    Adams, Gregory L.
    Carroll, Patrick J.
    Smith, Amos B., III
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2012, 134 (09) : 4037 - 4040
  • [2] [Anonymous], 2016, ANGEW CHEM, V128, P770
  • [3] [Anonymous], 2013, ANGEW CHEM, V125, P3354
  • [4] [Anonymous], 2009, ANGEW CHEM INT EDIT
  • [5] [Anonymous], 2016, ANGEW CHEM, V128, P3561
  • [6] [Anonymous], 2005, ANGEW CHEM, V117, P7084
  • [7] [Anonymous], 2014, ANGEW CHEM, V126, P1849
  • [8] Exploiting the palladium [0]-catalysed Ullmann cross-coupling reaction in natural products chemistry:: application to a total synthesis of the alkaloid (±)-aspidospermidine
    Banwell, MG
    Lupton, DW
    [J]. ORGANIC & BIOMOLECULAR CHEMISTRY, 2005, 3 (02) : 213 - 215
  • [9] An Electrophilic Bromine Redox Catalysis for the Synthesis of Indole Alkaloid Building Blocks by Selective Aliphatic C-H Animation
    Berges, Julien
    Garcia, Belen
    Muniz, Kilian
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2018, 57 (48) : 15891 - 15895
  • [10] Use of the Nosyl Group as a Functional Protecting Group in Applications of a Michael/Smiles Tandem Process
    Coulibali, Siomenan
    Godou, Timothe
    Canesi, Sylvain
    [J]. ORGANIC LETTERS, 2016, 18 (17) : 4348 - 4351