CHEMOSELECTIVE CARBONYL ALKYLATION AND REDUCTION OF ALDEHYDES OR KETONES

被引：54

作者：

MARUOKA, K ^{[1
]}

ARAKI, Y ^{[1
]}

YAMAMOTO, H ^{[1
]}

机构：

[1] NAGOYA UNIV,DEPT APPL CHEM,CHIKUSA KU,NAGOYA,AICHI 464,JAPAN

来源：

TETRAHEDRON LETTERS | 1988年 / 29卷 / 25期

关键词：

D O I：

10.1016/0040-4039(88)85096-2

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：3101 / 3104

页数：4

共 28 条

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[3] PENTACO-ORDINATE SILICON-COMPOUNDS IN SYNTHESIS - CHEMO-SELECTIVE AND STEREOSELECTIVE REDUCTION OF CARBONYL-COMPOUNDS USING TRIALKOXY-SUBSTITUTED SILANES AND ALKALI-METAL ALKOXIDES [J].

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[5] TRANSITION METAL-ACTIVATED ORGANIC-COMPOUNDS .20. ALDEHYDE SELECTIVITY OF ALKYL COMPLEXES OF SCANDIUM, YTTRIUM, LANTHANUM AND LANTHANIDES IN ALDEHYDE KETONE CONCURRENCE EXPERIMENTS [J].

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[7] METHYLALUMINUM BIS(2,6-DI-TERT-BUTYL-4-ALKYLPHENOXIDE) - A NEW REAGENT FOR OBTAINING UNUSUAL EQUATORIAL AND ANTI-CRAM SELECTIVITY IN CARBONYL ALKYLATION [J].

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[8] A NEW, STEREOCONTROLLED SYNTHESIS OF EQUATORIAL ALCOHOLS BY THE AMBIPHILIC REDUCTION OF CYCLOHEXANONES [J].

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[9] SELECTIVE REACTIONS USING ORGANO-ALUMINUM REAGENTS [J].

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ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1985, 24 (08) :668-682

[10] ORGANOALUMINUM-PROMOTED BECKMANN REARRANGEMENT OF OXIME SULFONATES [J].

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