Sulfinyl versus allylic stereocontrol in Diels-Alder cycloadditions of hydroxy 2-sulfinyl butadienes

被引：17

作者：

de la Pradilla, RF

Montero, C

Viso, A

机构：

[1] CSIC, Inst Quim Organ, E-28006 Madrid, Spain

[2] Univ Complutense Madrid, Fac Quim, Dept Quim Organ 1, E-28040 Madrid, Spain

来源：

CHEMICAL COMMUNICATIONS | 1998年 / 03期

关键词：

D O I：

10.1039/a708272j

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Enantiopure hydroxy 2-sulfinyl butadienes undergo a highly face selective Diels-Alder cycloaddition with N-phenylmaleimide and phenyltriazolinedione controlled by the chiral sulfur atom; the related enantiopure sulfonyl dienes display complimentary pi-facial selectivity.

引用

页码：409 / 410

页数：2

共 28 条

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