Total Synthesis of (±)-Aspidospermidine, (±)-Aspidofractinine, (±)-Limaspermidine, and (±)-Vincadifformine via a Cascade and Common Intermediate Strategy

被引:7
作者
Cain, David L. [1 ,2 ]
Anderson, Niall A. [3 ,4 ]
Cordes, David B. [1 ]
Slawin, Alexandra M. Z. [1 ]
Watson, Allan J. B. [1 ]
机构
[1] Univ St Andrews, Sch Chem, EaStCHEM, St Andrews KY16 9ST, Scotland
[2] Sygnature Discovery Bioc, Pennyfoot St, Nottingham NG1 1GR, England
[3] Med Res Ctr, GlaxoSmithKline, Stevenage SG12NY, England
[4] Unit 310, AstraZeneca, Darwin Bldg, Cambridge Sci Pk, Milton Rd, Cambridge CB4 0WG, England
基金
英国工程与自然科学研究理事会;
关键词
BIOMIMETIC ALKALOID SYNTHESES; ASYMMETRIC TOTAL-SYNTHESIS; ASPIDOSPERMA ALKALOIDS; PATTERN-RECOGNITION; MASS SPECTROMETRY; INDOLE ALKALOIDS; FORMAL SYNTHESIS; VINCADIFFORMINE; CYCLIZATION; LEUCONODINES;
D O I
10.1021/acs.joc.2c02099
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A concise strategy for the total synthesis of several Aspidosperma alkaloids is reported. A Suzuki-Miyaura cross-coupling provides access to a 2-vinyl indole that undergoes a Diels-Alder cascade reaction with butyn-2-one to deliver a pyrroloindoline intermediate. This undergoes cascade amidation, reduction, skeletal rearrangement, and intramolecular Michael addition to provide a common intermediate containing the full framework of the Aspidosperma alkaloids. The utility of this intermediate is shown in the synthesis of four different natural products.
引用
收藏
页码:15559 / 15563
页数:5
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