The first total synthesis of (±)-apparicine

被引：37

作者：

Bennasar, M. -Lluisa ^{[1
]}

Zulaica, Ester

Sole, Daniel

Alonso, Sandra

机构：

[1] Univ Barcelona, Fac Pharm, Organ Chem Lab, E-08028 Barcelona, Spain

来源：

CHEMICAL COMMUNICATIONS | 2009年 / 23期

关键词：

RING-CLOSING METATHESIS; STEREOCONTROLLED SYNTHESIS; OLEFIN ISOMERIZATION; CONCISE SYNTHESIS; ALKALOIDS; APPARICINE; CONSTRUCTION;

D O I：

10.1039/b903577j

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

The first total synthesis of the indole alkaloid apparicine has been developed through a sequence that includes an indole-templated ring-closing metathesis and a vinyl halide Heck cyclization.

引用

页码：3372 / 3374

页数：3

共 34 条

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