FACILE CLEAVAGE OF THE C-BETA-C-BETA'-BOND OF ZIRCONACYCLOPENTENES - CONVENIENT METHOD FOR SELECTIVELY COUPLING ALKYNES WITH ALKYNES, NITRILES, AND ALDEHYDES

被引：193

作者：

TAKAHASHI, T ^{[1
]}

KAGEYAMA, M ^{[1
]}

DENISOV, V ^{[1
]}

HARA, R ^{[1
]}

NEGISHI, E ^{[1
]}

机构：

[1] PURDUE UNIV,DEPT CHEM,W LAFAYETTE,IN 47907

来源：

TETRAHEDRON LETTERS | 1993年 / 34卷 / 04期

关键词：

D O I：

10.1016/S0040-4039(00)61653-2

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The reaction of zirconacyclopentenes (1) with alkynes, nitriles, and aldehydes proceeds via cleavage of the C(beta)-C(beta') bond of 1 and displacement of ethylene by the donors to give the corresponding five-membered zirconacycles, providing a convenient means of selectively coupling alkynes with pi-donor compounds.

引用

页码：687 / 690

页数：4

共 20 条

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