FAVORSKII REARRANGEMENTS .7. FORMATION OF AMIDES FROM ALPHA-HALO ALPHA'-ARYL KETONES

被引：17

作者：

BORDWELL, FG ^{[1
]}

ALMY, J ^{[1
]}

机构：

[1] NORTHWESTERN UNIV,DEPT CHEM,EVANSTON,IL 60201

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1973年 / 38卷 / 03期

关键词：

D O I：

10.1021/jo00943a035

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：571 / 575

页数：5

共 20 条

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[6] FAVORSKII REACTIONS .I. NATURE OF RATE-DETERMINING STEP [J].

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[7] FAVORSKII REARRANGEMENTS .4. MECHANISTIC CHANGE ON METHYL SUBSTITUTION [J].

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[8]

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[9] EVIDENCE FOR A DELOCALIZED INTERMEDIATE IN FAVORSKII REARRANGEMENT - 2,6-LUTIDINE-PROMOTED METHANOLYSIS OF ALPHA-CHLORODIBENZYL KETONE [J].

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[10] NONLINEAR STRUCTURE-REACTIVITY CORRELATIONS . REACTIVITY OF NUCLEOPHILIC REAGENTS TOWARD ESTERS [J].

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