AN UNUSUALLY HIGH EXO-ENDO RATE RATIO IN SOLVOLYSIS OF 2,6,6-TRIMETHYL-2-NORBORNYL P-NITROBENZOATES . FURTHER EVIDENCE FOR STERIC EFFECTS AS A MAJOR FACTOR IN EXO-ENDO RATE RATIOS OF NORBORNYL DERIVATIVES

被引：47

作者：

IKEGAMI, S

JAGT, DLV

BROWN, HC

机构：

来源：

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | 1968年 / 90卷 / 25期

关键词：

D O I：

10.1021/ja01027a044

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

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页码：7124 / &

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[1] AN UNUSUALLY LOW EXO-ENDO RATE RATIO IN SOLVOLYSIS OF 2,7,7-TRIMETHYL-2-NORBORNYL P-NITROBENZOATES . EVIDENCE FOR STERIC EFFECTS AS A MAJOR FACTOR IN EXO-ENDO RATE AND PRODUCT RATIOS OF NORBORNYL DERIVATIVES
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[2] RATES OF REACTION OF SODIUM BOROHYDRIDE WITH BICYCLIC KETONES STERIC APPROACH CONTROL AND STERIC DEPARTURE CONTROL IN REACTIONS OF RIGID BICYCLIC SYSTEMS
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[3] SLOW RATES OF SOLVOLYSIS OF ENDO-5,6-TRIMETHYLENE-ENDO-(2 AND 8)-NORBORNYL TOSYLATES - STERIC HINDRANCE TO IONIZATION AND FOOTE-SCHLEYER CORRELATION
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[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1968, 90 (22) : 6216 - &
[5] SOLVOLYSIS OF OPTICALLY ACTIVE 1,2-DIMETHYL-EXO-2-NORBORNYL P-NITROBENZOATE . EVIDENCE FOR INVOLVEMENT OF A CLASSICAL CARBONIUM ION
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