A new radical-based route to calothrixin B

被引：67

作者：

Bennasar, ML ^{[1
]}

Roca, T ^{[1
]}

Ferrando, F ^{[1
]}

机构：

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

来源：

ORGANIC LETTERS | 2006年 / 8卷 / 04期

关键词：

D O I：

10.1021/ol052600e

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A high-hielding totally regioselective intramolecular homolytic acylation of a quinoline ring constitutes the key step in a new synthesis of the pentacyclic indolo[3,2j]phenanthridine alkaloid calothrixin B.

引用

页码：561 / 564

页数：4

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