CONDENSATIONS AT TERMINAL METHYL GROUP OF 1,3,5-TRIKETONES BY MEANS OF SODAMIDE IN LIQUID AMMONIA

被引：25

作者：

HAMPTON, KG

HARRIS, TM

HARRIS, CM

HAUSER, CR

机构：

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1965年 / 30卷 / 12期

关键词：

D O I：

10.1021/jo01023a062

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：4263 / &

共 11 条

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HAUSER, CR .

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[3] MONO- VS DIALKYLATION OF ACETYLACETONE WITH ALKYL HALIDES THROUGH DIALKALI SALTS - METALLIC CATION EFFECT [J].

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HARRIS, TM ;

HAUSER, CR .

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[4] CONDENSATIONS AT THE METHYL GROUP RATHER THAN THE METHYLENE GROUP OF BENZOYLACETONE AND ACETYLACETONE THROUGH INTERMEDIATE DIPOTASSIO SALTS [J].

HAUSER, CR ;

HARRIS, TM .

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[5]

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HAUSER, CR .

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[7] AROYLATIONS OF BETA-DIKETONES AT THE TERMINAL METHYL GROUP TO FORM 1,3,5-TRIKETONES - CYCLIZATIONS TO 4-PYRONES AND 4-PYRIDONES [J].

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[8] AROYLATION AT TERMINAL METHYL GROUP OF A 1,3,5-TRIKETONE TO FORM A 1,3,5,7-TETRAKETONE [J].

MILES, ML ;

HARRIS, TM ;

HAUSER, CR .

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[9] AROYLATIONS AT METHYL GROUP OF BENZOYLACETONE AND RELATED BETA-DIKETONES WITH ESTERS TO FORM 1,3,5-TRIKETONES BY SODIUM HYDRIDE . OTHER TERMINAL CONDENSATIONS [J].

MILES, ML ;

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HAUSER, CR .

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[10]

MILES ML, PRIVATE COMMUNICATIO

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