REACTIONS OF 9-SUBSTITUTED FLUORENIDE CARBANIONS WITH ALLYL CHLORIDES BY SN2 AND SN2' MECHANISMS

被引：22

作者：

BORDWELL, FG

CLEMENS, AH

CHENG, JP

机构：

来源：

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | 1987年 / 109卷 / 06期

关键词：

D O I：

10.1021/ja00240a029

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

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页码：1773 / 1782

页数：10

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[3] BRONSTED CORRELATIONS FOR ELECTRON-TRANSFER FROM CARBANIONS TO HALOMETHYL PHENYL SULFONE AND 1,1-DINITROALKANE-TYPE ACCEPTORS
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[5] HAMMETT AND BRONSTED-TYPE RELATIONSHIPS IN REACTIONS OF 9-SUBSTITUTED FLUORENYL ANIONS WITH BENZYL HALIDES
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[6] CORRELATION BETWEEN THE BASICITY OF CARBANIONS AND THEIR ABILITY TO TRANSFER AN ELECTRON
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[7] HOW COMMON ARE BASE-INITIATED, CONCERTED 1,2 ELIMINATIONS
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[8] RATE EQUILIBRIUM RELATIONSHIPS FOR REACTIONS OF FAMILIES OF CARBANION NUCLEOPHILES WITH N-BENZYL-N,N-DIMETHYLANILINIUM CATIONS AND WITH ALKYL CHLORIDES, BROMIDES, AND IODIDES
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[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1986, 108 (23) : 7300 - 7309
[9] STERIC, CONFORMATIONAL, AND ELECTRONIC EFFECTS AS REVEALED BY ACIDITIES OF SUBSTITUTED XANTHENES AND REACTIONS OF SUBSTITUTED XANTHENYL AND RELATED CARBANIONS WITH BENZYL-CHLORIDE
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[10] BORDWELL FG, 1982, J ORG CHEM, V47, P3803

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