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导向费歇尔吲哚化法在(+)-阿朴斯多辛和(-)-塔博沙林全合成中的应用。

Directed Fischer Indolization as an Approach to the Total Syntheses of (+)-Aspidospermidine and (-)-Tabersonine.

机构信息

Center for New Directions in Organic Synthesis, Department of Chemistry, Hanyang University , 222 Wangshimni-ro, Seongdong-gu, Seoul 04763, Korea.

出版信息

Org Lett. 2017 Nov 17;19(22):6168-6171. doi: 10.1021/acs.orglett.7b03078. Epub 2017 Nov 9.

Abstract

A conceptually new synthetic approach that provides general access to the aspidosperma alkaloids (+)-aspidospermidine and (-)-tabersonine was developed. This method is based on the regioselective indolization of an ene-hydrazide, which was obtained via a base-catalyzed intramolecular aza-Michael reaction, in situ trapping of the resulting enolate, and subsequent C-N coupling with phenyl hydrazide.

摘要

开发了一种概念新颖的合成方法,可广泛获得(aspidosperma alkaloids)(+)-aspidospermidine 和 (-)-tabersonine。该方法基于烯腙的区域选择性吲哚化,烯腙是通过碱催化的分子内氮杂迈克尔反应原位捕获生成的烯醇化物,以及随后与苯肼的 C-N 偶联得到的。

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