SYNTHETIC ANTHRACYCLINES FROM ANTHRAQUINONES - INVITED REVIEW

被引：17

作者：

CAMBIE, RC ^{[1
]}

RUTLEDGE, PS ^{[1
]}

WOODGATE, PD ^{[1
]}

机构：

[1] UNIV AUCKLAND,DEPT CHEM,AUCKLAND,NEW ZEALAND

来源：

AUSTRALIAN JOURNAL OF CHEMISTRY | 1992年 / 45卷 / 03期

关键词：

D O I：

10.1071/CH9920483

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Our syntheses of important and novel daunomycinones, aklavinones, fridamycins and vineomycinones, from 1,4- or 1,5-dihydroxyanthraquinones, are reviewed. The reductive Claisen rearrangement has proven to be the most versatile of the methods developed for appending rings or functionalized side chains. Some novel polycyclic systems have been made, some interesting new properties of substituted quinizarins and anthrarufins uncovered, and new methods for elaboration of allyl systems developed.

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页码：483 / 512

页数：30

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