HIGH EXO - ENDO RATE RATIO AND PREDOMINANT EXO SUBSTITUTION IN SOLVOLYSIS OF 2 PARA ANISYL-2-NORBORNENYL DERIVATIVES - EVIDENCE FOR A HIGH EXO-ENDO RATE RATIO IN A 2-NORBORNENYL DERIVATIVE SOLVOLYZING WITHOUT SIGNIFICANT PI PARTICIPATION

被引：13

作者：

PETERS, EN

BROWN, HC

机构：

来源：

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | 1972年 / 94卷 / 16期

关键词：

D O I：

10.1021/ja00771a063

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：5899 / &

共 12 条

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[3] RATES OF SOLVOLYSIS OF RHO-NITROBENZOATES OF EXO-ENDO TERTIARY NORBORNEOLS . CRITICAL EXAMINATION OF EXO-ENDO RATE RATIO AS BASIS FOR POSTULATED NONCLASSICAL STRUCTURE OF NORBORNYL CATION [J].

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[4] SOLVOLYSIS OF 2-ARYLBENZONORBORNEN-2-YL P-NITROBENZOATES CONTAINING REPRESENTATIVE SUBSTITUENTS IN 2-ARYL GROUP . CONSTANCY IN EXO/ENDO RATE RATIO WITH INCREASING ELECTRON DEMAND BY 2-ARYL GROUP [J].

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LIU, KT .

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[5]

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[6]

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[7]

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[9] EQUILIBRATION OF 2-METHYLNORBORNANOLS . A FAST ACID-CATALYZED CONVERSION OF 2-METHYL-EXO-NORBORNANOL INTO 2-METHYL-ENDO-NORBORNANOL [J].

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BROWN, HC .

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[10] DRIVING FORCE OF THE HOMOALLYLIC REARRANGEMENT IN ACETOLYSIS OF EXO-DEHYDRONORBORNYL PARA-BROMOBENZENESULFONATE [J].

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