Diastereoselective synthesis of dimethyl cyclopropane-1,1-dicarboxylates from a γ-alkoxy-alkylidene malonate and sulfur and phosphorus ylides

被引：38

作者：

Krief, A ^{[1
]}

Provins, L ^{[1
]}

Froidbise, A ^{[1
]}

机构：

[1] Fac Univ Notre Dame Paix, Dept Chem, Lab Chim Organ Synthese, B-5000 Namur, Belgium

来源：

TETRAHEDRON LETTERS | 1998年 / 39卷 / 11期

关键词：

D O I：

10.1016/S0040-4039(97)10822-X

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Isopropylidene diphenylsulfurane and isopropylidene triphenylphosphorane react by the same (Re) face of the alkylidene malonate derived from the acetonide of (d)glyceraldehyde to produce almost exclusively a single diastereoisomer of the corresponding dimethyl cyclopropane-l,l-dicarboxylate. (C) 1998 Elsevier Science Ltd. All rights reserved.

引用

页码：1437 / 1440

页数：4

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