A synthetic approach to benanomicin A .1. Synthesis of 5,6-dihydrobenzo[a]naphthacenequinone

被引：5

作者：

Hirosawa, S ^{[1
]}

Nishizuka, T ^{[1
]}

Kondo, S ^{[1
]}

Ikeda, D ^{[1
]}

Takeuchi, T ^{[1
]}

机构：

[1] INST MICROBIAL CHEM,MCRF,SHINAGAWA KU,TOKYO 141,JAPAN

来源：

JOURNAL OF ANTIBIOTICS | 1997年 / 50卷 / 08期

关键词：

D O I：

10.7164/antibiotics.50.685

中图分类号：

Q81 [生物工程学（生物技术）]; Q93 [微生物学];

学科分类号：

071005 ; 0836 ; 090102 ; 100705 ;

摘要：

5,6-Dihydrobenzo[a]naphthacenequinone has been constructed by DIELS-ALDER reaction of an outer-ring diene with a naphthoquinone regioselectively. Similarly, the 14-hydroxy-5,6-dihydrobenzo[a]naphthacenequinone (13) has also been synthesized via the reaction of vinylketene acetal (11) with naphthoquinone.

引用

页码：685 / 689

页数：5

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