Facile synthesis of terminal 1,2-diols with high optical purity via oxazaborolidine-catalyzed asymmetric borane reduction

被引：35

作者：

Cho, BT ^{[1
]}

Chun, YS ^{[1
]}

机构：

[1] Hallym Univ, Dept Chem, Kangwondo 200702, South Korea

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1998年 / 63卷 / 15期

关键词：

D O I：

10.1021/jo980455v

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：5280 / 5282

页数：3

共 33 条

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[5] ASYMMETRIC REDUCTION OF ALPHA-KETO ACETALS WITH POTASSIUM 9-O-(1,2-ISOPROPYLIDENE-5-DEOXY-D-XYLOFURANOSYL)-9-BORATABICYCLO[3.3.1]NONANE - ENANTIOSELECTIVE SYNTHESIS OF ALPHA-HYDROXY ACETALS WITH HIGH OPTICAL PURITIES
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[7] Asymmetric synthesis of (S)-carbinoxamine. New aspects of oxazaborolidine-catalyzed enantioselective carbonyl reduction
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[8] A NEW SYSTEM FOR CATALYTIC ENANTIOSELECTIVE REDUCTION OF ACHIRAL KETONES TO CHIRAL ALCOHOLS - SYNTHESIS OF CHIRAL ALPHA-HYDROXY ACIDS
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[9] A CATALYTIC ENANTIOSELECTIVE SYNTHESIS OF DENOPAMINE, A USEFUL DRUG FOR CONGESTIVE-HEART-FAILURE
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[10] HIGHLY ENANTIOSELECTIVE BORANE REDUCTION OF KETONES CATALYZED BY CHIRAL OXAZABOROLIDINES - MECHANISM AND SYNTHETIC IMPLICATIONS
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