Regio- and stereoselective ring opening of epoxides.: Enantioselective synthesis of 2,3,4-trisubstituted five-membered heterocycles

被引：20

作者：

Díez, D ^{[1
]}

Beneitez, MT ^{[1
]}

Marcos, IS ^{[1
]}

Garrido, NM ^{[1
]}

Basabe, P ^{[1
]}

Urones, JG ^{[1
]}

机构：

[1] Univ Salamanca, Fac Ciencias Quim, Dept Quim Organ, E-37008 Salamanca, Spain

来源：

TETRAHEDRON-ASYMMETRY | 2002年 / 13卷 / 06期

关键词：

D O I：

10.1016/S0957-4166(02)00160-X

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

By using the appropriate protecting groups. the opening of (2S.3S.4E)-5-benzenesulfonyl-2.3-epoxy-pent-4-en-1-ol (-)-2 could be controlled and used for the synthesis of the enantiomeric pyrrolidines (+)- and (-)-18 and the tetrahydrofuran analogs (+)- and (-)-19. (C) 2002 Elsevier Science Ltd. All rights reserved.

引用

页码：639 / 646

页数：8

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