SPONTANEOUS AND BASE-CATALYZED ELIMINATION FROM 1-FERROCENYLALKYL CATIONS

被引：12

作者：

BUNTON, CA ^{[1
]}

CARRASCO, N ^{[1
]}

DAVOUDZADEH, F ^{[1
]}

机构：

[1] UNIV ULSTER,SCH PHYS SCI,COLERAINE BT52 1SA,NORTH IRELAND

来源：

JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2 | 1981年 / 06期

关键词：

D O I：

10.1039/p29810000924

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：924 / 930

页数：7

共 39 条

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[7] KINETIC ISOTOPE EFFECTS AS GUIDES TO TRANSITION-STATE STRUCTURES IN DEPROTONATION REACTIONS
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[8] COMPARISON OF MERCAPTIDE AND ALKOXIDE IONS AS REAGENTS FOR OLEFIN-FORMING BETA ELIMINATION
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[9] STABLE CARBOCATIONS .22. STEREOCHEMISTRY OF THE DEPROTONATION OF FERROCENYLALKYLIUM IONS, AND OF THE PROTONATION OF ALKENYLFERROCENES
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[J]. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1980, (10): : 2213 - 2217
[10] REACTIONS OF TRI PARA ANISYLMETHYL CARBONIUM-ION WITH NUCLEOPHILES
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HUANG, SK
[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1972, 94 (10) : 3536 - &

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