Nickel-catalyzed tandem coupling of allyl electrophiles, alkynes, and alkynyltins

被引：31

作者：

Cui, DM ^{[1
]}

Tsuzuki, T ^{[1
]}

Miyake, K ^{[1
]}

Ikeda, S ^{[1
]}

Sato, Y ^{[1
]}

机构：

[1] Nagoya City Univ, Dept Pharmaceut Sci, Mizuho Ku, Nagoya, Aichi 467, Japan

来源：

TETRAHEDRON | 1998年 / 54卷 / 07期

关键词：

D O I：

10.1016/S0040-4020(97)10207-1

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The nickel-catalyzed intermolecular coupling of allyl acetate or allyl carbonate with alkynes and alkynyltins was carried out in the presence of LiCl to give 3,6-dien-1-yne regio-and stereoselectively. On the other hand, the intramolecular cyclization and coupling of omega-alkynyl electrophiles with alkynyltins gave five-membered cyclic products. (C) 1998 Elsevier Science Ltd. All rights reserved.

引用

页码：1063 / 1072

页数：10

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