The synthesis of the C15-C24 segment of ratjadone

被引：10

作者：

Christmann, M ^{[1
]}

Kalesse, M ^{[1
]}

机构：

[1] Univ Hannover, Inst Organ Chem, D-30167 Hannover, Germany

来源：

TETRAHEDRON LETTERS | 1999年 / 40卷 / 40期

关键词：

D O I：

10.1016/S0040-4039(99)01486-0

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Ratjadone is an antifungal and highly cytotoxic polyketide from Sorangium cellulosum. The tetrahydropyran ring is supposed to result from an intramolecular opening of a C16-C17 epoxide. Herein we report the biomimetic synthesis of the C15-C24 segment of ratjadone. (C) 1999 Elsevier Science Ltd. Ali rights reserved.

引用

页码：7201 / 7204

页数：4

共 21 条

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