An efficient synthesis of sulfobacin A (flavocristamide B), sulfobacin B, and flavocristamide A

被引：27

作者：

Shioiri, T ^{[1
]}

Irako, N ^{[1
]}

机构：

[1] Nagoya City Univ, Fac Pharmaceut Sci, Mizuho Ku, Nagoya, Aichi 4678603, Japan

来源：

TETRAHEDRON | 2000年 / 56卷 / 46期

关键词：

sulfonolipids; asymmetric aldol reaction; 2-hydroxy-3-pinanone; oxidation;

D O I：

10.1016/S0040-4020(00)00768-7

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Sulfobacin A (flavocristamide B, 1), sulfobacin B (2), and flavocristamide A (3), biologically active sulfonolipids, have been efficiently synthesized utilizing the asymmetric aldol reaction of the Schiff base 8 derived from glycine eater and (+)-2-hydroxy-3-pinanone (HyPN). (C) 2000 Elsevier Science Ltd. All rights reserved.

引用

页码：9129 / 9142

页数：14

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