AN INTRODUCTION OF CHIRAL CENTERS INTO ACYCLIC SYSTEMS BASED ON STEREOSELECTIVE KETONE REDUCTION

被引：251

作者：

OISHI, T

NAKATA, T

机构：

来源：

ACCOUNTS OF CHEMICAL RESEARCH | 1984年 / 17卷 / 09期

关键词：

D O I：

10.1021/ar00105a007

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

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页码：338 / 344

页数：7

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[41] STEREOSELECTIVE SYNTHESIS OF THE FUNCTIONALIZED SYN-1,3,5,7-TETRAOL
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[42] STEREOSELECTIVE ACYCLIC KETONE REDUCTION - SYNTHESIS OF THE SYNTHONS HAVING 3 CONSECUTIVE CHIRAL CENTERS
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[48] ASYMMETRIC REDUCTION BY YEASTS - FORMATION OF OPTICALLY-ACTIVE SYNTHONS HAVING 2 CHIRAL CENTERS USEFUL FOR NATURAL PRODUCT SYNTHESIS
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[49] MARINE NATURAL-PRODUCTS FROM THE ATLANTIC ZONE .30. HIGHLY STEREOCONTROLLED REDUCTION OF ALPHA'-ALKOXYENONES TO GIVE EITHER THE THREO ORERYTHRO ALLYLIC 1,2-DIOL - ASSIGNMENT OF THE THREO CONFIGURATION TO THE C-15,C-16 DIOL OF PUMILIOTOXIN-B
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[J]. TETRAHEDRON LETTERS, 1982, 23 (23) : 2355 - 2358
[50] SYNTHESIS AND MOLECULAR-STRUCTURE OF THE NIOBOCENE-CARBONYLHYDRIDE ADDUCT TO BIS-(TETRAHYDROBORATE)-ZINC
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