CONVERGENT SYNTHESIS OF STREPTONIGRIN AND LAVENDAMYCIN ANALOGS

被引：33

作者：

GODARD, A ^{[1
]}

ROCCA, P ^{[1
]}

FOURQUEZ, JM ^{[1
]}

ROVERA, JC ^{[1
]}

MARSAIS, F ^{[1
]}

QUEGUINER, G ^{[1
]}

机构：

[1] INST NATL SCI APPL ROUEN,CNRS,CHIM ORGAN FINE & HETEROCYCL LAB,F-76131 MONT ST AIGNAN,FRANCE

来源：

TETRAHEDRON LETTERS | 1993年 / 34卷 / 49期

关键词：

ALKALOID; CROSS-COUPLING; LAVENDAMYCIN; METALATION; OXIDATIVE DEMETHYLATION; PALLADIUM; STREPTONIGRIN;

D O I：

10.1016/S0040-4039(00)61511-3

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A convergent synthesis of streptonigrin and lavendamycin analogues incorporating a quinoline-5,8-dione structure is reported. The approach is based on our synthetic methodology which involves such reactions as metalation, heteroring cross-coupling and oxidative demethylation.

引用

页码：7919 / 7922

页数：4

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