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Synthesis of the furanosteroidal antibiotic viridin
被引:106
作者
:
Anderson, EA
论文数:
0
引用数:
0
h-index:
0
机构:
Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA
Anderson, EA
Alexanian, EJ
论文数:
0
引用数:
0
h-index:
0
机构:
Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA
Alexanian, EJ
Sorensen, EJ
论文数:
0
引用数:
0
h-index:
0
机构:
Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA
Sorensen, EJ
机构
:
[1]
Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA
[2]
Scripps Res Inst, Skaggs Inst Chem Biol, La Jolla, CA 92037 USA
[3]
Princeton Univ, Dept Chem, Princeton, NJ 08544 USA
来源
:
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
|
2004年
/ 43卷
/ 15期
关键词
:
cyclotrimerization;
dihydroxylation;
electrocyclic reactions;
inhibitors;
natural products;
D O I
:
10.1002/anie.200353129
中图分类号
:
O6 [化学];
学科分类号
:
0703 ;
摘要
:
A rhodium-catalyzed alkyne cyclotrimerization, domino electrocyclic reactions, and a hydroxy-directed dihydroxylation are key steps in an efficient synthesis of the bioactive furanosteroid viridin (1) from a simple acyclic triyne.
引用
收藏
页码:1998 / 2001
页数:4
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