STERIC EFFECTS IN ELIMINATION REACTIONS .4. THE QUESTION OF REARRANGEMENTS AS A FACTOR IN THE EXTENT AND DIRECTION OF UNIMOLECULAR ELIMINATION

被引：17

作者：

BROWN, HC

OKAMOTO, Y

机构：

来源：

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | 1955年 / 77卷 / 13期

关键词：

D O I：

10.1021/ja01618a057

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：3619 / 3623

页数：5

共 15 条

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[4] STRUCTURE OF THE CHLORIDES FROM 2,2,3-TRIMETHYL-3-PENTANOL AND 2,3,3-TRIMETHYL-2-PENTANOL - STERIC EFFECTS AS A FACTOR IN THE REARRANGEMENTS OF HIGHLY BRANCHED CARBONIUM IONS [J].

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[5] CHEMICAL EFFECTS OF STERIC STRAINS .2. THE EFFECT OF STRUCTURE ON OLEFIN FORMATION IN THE HYDROLYSIS OF TERTIARY ALIPHATIC CHLORIDES [J].

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[6] STERIC EFFECTS IN ELIMINATION REACTIONS .1. DIRECTIVE EFFECTS IN UNIMOLECULAR ELIMINATIONS - A CASE OF HOFMANN RULE ELIMINATION IN AN E1 REACTION [J].

BROWN, HC ;

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JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1955, 77 (13) :3607-3610

[7] STERIC EFFECTS IN ELIMINATION REACTIONS .3. THE EFFECT OF THE STERIC REQUIREMENTS OF ALKYL SUBSTITUENTS UPON THE EXTENT AND DIRECTION OF UNIMOLECULAR ELIMINATION IN THE SOLVOLYSIS OF SECONDARY ALKYL BROSYLATES [J].

BROWN, HC ;

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[8] STERIC EFFECTS IN ELIMINATION REACTIONS .2. THE EFFECT OF THE STERIC REQUIREMENTS OF ALKYL SUBSTITUENTS UPON THE EXTENT AND DIRECTION OF UNIMOLECULAR ELIMINATION IN THE SOLVOLYSIS OF TERTIARY ALKYL BROMIDES [J].

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NAKAGAWA, M .

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[9]

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[10] MECHANISM OF ELIMINATION REACTIONS .17. THE COMPARATIVE UNIMPORTANCEOF STERIC STRAIN IN UNIMOLECULAR OLEFIN ELIMINATION [J].

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