STRUCTURE AND EFFICIENCY IN INTRAMOLECULAR AND ENZYMIC CATALYSIS - CATALYSIS OF AMIDE HYDROLYSIS BY CARBOXY-GROUP OF SUBSTITUTED MALEAMIC ACIDS

被引：197

作者：

KIRBY, AJ

LANCASTER, PW

机构：

来源：

JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2 | 1972年 / 09期

关键词：

D O I：

10.1039/p29720001206

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

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页码：1206 / +

页数：1

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[1] RATE-DETERMINING PROTON-TRANSFER IN INTRAMOLECULAR CATALYSIS OF AMIDE HYDROLYSIS BY CARBOXYLIC-ACID GROUP
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[9] GEM EFFECT .4. ACTIVATION PARAMETERS ACCOMPANYING INCREASED STERIC REQUIREMENTS OF 3,5' SUBSTITUENTS IN SOLVOLYSIS OF MONO-P-BROMOPHENYL GLUTARATES
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[10] GEM EFFECT .3. INFLUENCE OF 3-MONO- AND 3-GEM SUBSTITUTION ON ACID DISSOCIATION CONSTANTS OF GLUTARIC ACID . A COMPARISON OF SENSITIVITY OF DELTAPKA OF DICARBOXYLIC ACIDS AND RATE OF RING CLOSURE OF THEIR MONOESTERS TO INTRAMOLECULAR DISTANCE SEPARATING CARBOXYL FUNCTIONS
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