STERIC EFFECTS IN DISPLACEMENT REACTIONS .6. THE HEATS OF FORMATION OF THE ADDITION COMPOUNDS OF BORON TRIFLUORIDE WITH THE MONOALKYLPYRIDINES - A LINEAR RELATIONSHIP INVOLVING STERICALLY HINDERED REACTANTS

被引：35

作者：

BROWN, HC

HOROWITZ, RH

机构：

来源：

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | 1955年 / 77卷 / 07期

关键词：

D O I：

10.1021/ja01612a005

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

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页码：1733 / 1737

页数：5

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[1] STERIC EFFECTS IN DISPLACEMENT REACTIONS .5. THE HEAT OF REACTION OF PYRIDINE WITH BORON TRIFLUORIDE - A CONVENIENT CALORIMETER FOR MEASURING THE HEAT OF FORMATION OF MOLECULAR ADDITION COMPOUNDS
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[2] A CONVENIENT SYNTHESIS OF THE MONOALKYLPYRIDINES - A NEW PROTOTROPIC REACTION OF 3-PICOLINE
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[3] STERIC EFFECTS IN DISPLACEMENT REACTIONS .3. THE BASE STRENGTHS OF PYRIDINE, 2,6-LUTIDINE AND THE MONOALKYLPYRIDINES
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[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1955, 77 (07) : 1723 - 1726
[4] STERIC EFFECTS IN DISPLACEMENT REACTIONS .2. THE RATES OF REACTION OF ALKYL IODIDE S WITH THE MONOALKYLPYRIDINES - STERIC STRAIN IN THE ACTIVATED COMPLEX
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[5] STERIC EFFECTS IN DISPLACEMENT REACTIONS .4. HEATS OF REACTION OF METHANESULFONIC ACID WITH THE MONOALKYLPYRIDINES
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[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1955, 77 (07) : 1727 - 1730
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[9] THE GENERAL NATURE OF THE PROPORTIONALITY OF POLAR EFFECTS OF SUBSTITUENT GROUPS IN ORGANIC CHEMISTRY
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[10] POLAR AND STERIC SUBSTITUENT CONSTANTS FOR ALIPHATIC AND O-BENZOATE GROUPS FROM RATES OF ESTERIFICATION AND HYDROLYSIS OF ESTERS
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