Total synthesis and revision of absolute stereochemistry of antillatoxin, an ichthyotoxic cyclic lipopeptide from marine cyanobacterium Lyngbya majuscula

被引:34
作者
Yokokawa, F [1 ]
Fujiwara, H [1 ]
Shioiri, T [1 ]
机构
[1] Nagoya City Univ, Fac Pharmaceut Sci, Mizuho Ku, Nagoya, Aichi 4678603, Japan
关键词
antillatoxin; ichthyotoxicity; cyclic lipopeptide; total synthesis;
D O I
10.1016/S0040-4020(00)00081-8
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Antillatoxin is an ichthyotoxic cyclic lipopeptide isolated by Gerwick and co-workers from the marine cyanobacterium Lyngbya majuscula collected in Curacao. Although we have finished the stereoselective total synthesis of antillatoxin having the proposed structure with (4S,5R)-configuration, we have found that the synthetic sample was not identical with the natural one and the proposed structure should be revised. Further our synthetic efforts have culminated in the first total synthesis of antillatoxin in its natural form, proving that the natural one has (4R,5R)-configuration. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1759 / 1775
页数:17
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