A convenient preparation of taxoid right-half building blocks

被引：13

作者：

Arseniyadis, S ^{[1
]}

del Moral, JQ

Alves, RB

Potier, P

Toupet, L

机构：

[1] CNRS, Inst Chim Subst Nat, F-91198 Gif Sur Yvette, France

[2] Univ Rennes 1, CNRS, URA 804, F-35042 Rennes, France

来源：

TETRAHEDRON-ASYMMETRY | 1998年 / 9卷 / 16期

关键词：

D O I：

10.1016/S0957-4166(98)00289-4

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

Wieland-Miescher ketone derived unsaturated diols 4 reacted with Pb(OAc)(4) to furnish tricyclic enolether intermediate 6 which upon ozonolysis gave access to useful synthetic intermediates such as bicyclic lactone 7, methyl furanoside 8 and triol 9 (taxoid right-half precursors), depending on the solvent used during the ozonolysis and the nature of the following synthetic operation. (C) 1998 Elsevier Science Ltd. All rights reserved.

引用

页码：2871 / 2878

页数：8

共 12 条

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