Alternative synthesis of B/C-cis hexahydrobenzo[c]-phenanthridine from 2-phenyl-1-tetralone

被引：0

作者：

Yoshida, M ^{[1
]}

Watanabe, T ^{[1
]}

Ishikawa, T ^{[1
]}

机构：

[1] Chiba Univ, Fac Pharmaceut Sci, Chiba 2638522, Japan

来源：

HETEROCYCLES | 2001年 / 54卷 / 01期

关键词：

reductive amidation; formenamide; Bischler-Napieralski reaction; hydride reduction;

D O I：

暂无

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A B/C-cis hexahydrobenzo[c]phenanthridine (7) was alternatively prepared by the hydride-reduction of a tetrahydrobenzo[c]phenanthridine derivative (6) under acidic condition, which was derived from 2-phenyl-1-tetralone oxime (3) through four steps (reductive amidation, methylation, Bischler-Napieralski cyclization, and hydride reduction).

引用

页码：433 / 436

页数：4

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