An Iminium Ion Cascade Annulation Strategy for the Synthesis of Akuammiline Alkaloid Pentacyclic Core Structures

被引:22
作者
Andreansky, Eric S. [1 ]
Blakey, Simon B. [1 ]
机构
[1] Emory Univ, Dept Chem, 1515 Pierce Dr, Atlanta, GA 30322 USA
基金
美国国家科学基金会;
关键词
FORMAL TOTAL-SYNTHESIS; STRYCHNOS ALKALOIDS; DIOLEFIN COMPLEXES; INDOLE ALKALOIDS; (+/-)-ASPIDOPHYLLINE; (+/-)-STRICTAMINE; CYCLIZATION; (+)-SCHOLARISINE; CONSTRUCTION; STRICTAMINE;
D O I
10.1021/acs.orglett.6b03406
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The akuammiline alkaloids are a family of indole monoterpene natural products known for their polycyclic cage like structures. An iminium ion cascade annulation approach was developed, simultaneously synthesizing both the C and D rings of these natural products by annulation onto a protected indole ring. This reaction allowed the synthesis of a key tetracyclic intermediate toward these natural products. This tetracycle was used for the synthesis of the pentacyclic methanoquinolizidine core present in such alkaloids as akuammiline and strictamine as well as the pentacyclic furoindoline core found in pseudoakuammigine.
引用
收藏
页码:6492 / 6495
页数:4
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