SPECTROSCOPIC AND CHEMICAL EVIDENCE FOR THE REVERSIBLE FORMATION OF VINYLCOPPER INTERMEDIATES IN THE STANNYLCUPRATION OF TERMINAL ALKYNES

被引：17

作者：

HUTZINGER, MW ^{[1
]}

SINGER, RD ^{[1
]}

OEHLSCHLAGER, AC ^{[1
]}

机构：

[1] SIMON FRASER UNIV,DEPT CHEM,BURNABY V5A 1S6,BC,CANADA

来源：

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | 1990年 / 112卷 / 25期

关键词：

D O I：

10.1021/ja00181a054

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

[No abstract available]

引用

页码：9397 / 9398

页数：2

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[4] REGIOSELECTIVE ADDITION OF TRIMETHYLSTANNYLCOPPER DIMETHYL SULFIDE TO 1-ALKYNES - SYNTHESIS OF OMEGA-SUBSTITUTED 2-(TRIMETHYLSTANNYL)-1-ALKENES [J].

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[5] SCOPE AND MECHANISM OF STANNYLALUMINATION OF 1-ALKYNES [J].

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[6]

WESTMIJZE H, 1982, TETRAHEDRON LETT, P2797

[7] STEREOSELECTIVE SYNTHESES OF SUBSTITUTED ENYNES, DIENES, AND ALKENES VIA STANNYLATION OF 1-TRIMETHYLSILYL 1,3-DIYNES [J].

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