A NEW SYNTHESIS OF 3-CHLORO BUTENOLIDES VIA REARRANGEMENT OF 3,3-DICHLORO BETA LACTONES

被引：8

作者：

BLACK, TH

MCDERMOTT, TS

机构：

[1] Department of Chemistry, Eastern Illinois University, Charleston, Illinois

来源：

SYNTHETIC COMMUNICATIONS | 1990年 / 20卷 / 19期

关键词：

D O I：

10.1080/00397919008051512

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

4,4-Dialkyl 3,3-dichlaro oxetan-2-ones rearrange under Lewis acid catalysis, accompanied by loss of HC1, to afford 4,5-dialkyl 3-chloro butenolides. © 1990, Taylor & Francis Group, LLC. All rights reserved.

引用

页码：2959 / 2964

页数：6

共 14 条

[11]

MEUL T, 1987, CHIMIA, V41, P73

[12] STEREOSPECIFIC SYNTHESIS OF GAMMA-LACTONES BY DYOTROPIC WAGNER-MEERWEIN REARRANGEMENT [J].

MULZER, J ;

BRUNTRUP, G .

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1979, 18 (10) :793-794

[13] CYCLOADDITION OF DICHLOROKETENE WITH FUNCTIONALIZED CYCLOALKENES - SYNTHESIS OF BICYCLO[4.2.0]OCTANONE-3-YL DERIVATIVES AND OF 3,4-DICARBOMETHOXY-1-METHYLBICYCLO[4.2.0]OCTAN-7-ONE [J].

ROSINI, G ;

BALLINI, R ;

ZANOTTI, V .

TETRAHEDRON, 1983, 39 (07) :1085-1090

[14] A NEW SYNTHETIC METHOD OF 3-ACYLTETRONIC ACID-DERIVATIVES AND ITS APPLICATION TO THE SYNTHESIS OF ISOASPERTETRONIN A(ISOGREGATIN A) [J].

TAKEDA, K ;

KUBO, H ;

KOIZUMI, T ;

YOSHII, E .

TETRAHEDRON LETTERS, 1982, 23 (31) :3175-3178

← 1 2 →