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
收藏
页码：338 / 344
页数：7
相关论文
共 58 条
[41]   STEREOSELECTIVE SYNTHESIS OF THE FUNCTIONALIZED SYN-1,3,5,7-TETRAOL [J].
NAKATA, T ;
TAKAO, S ;
FUKUI, M ;
TANAKA, T ;
OISHI, T .
TETRAHEDRON LETTERS, 1983, 24 (36) :3873-3876
[42]   STEREOSELECTIVE ACYCLIC KETONE REDUCTION - SYNTHESIS OF THE SYNTHONS HAVING 3 CONSECUTIVE CHIRAL CENTERS [J].
NAKATA, T ;
FUKUI, M ;
OHTSUKA, H ;
OISHI, T .
TETRAHEDRON, 1984, 40 (12) :2225-2231
[43]  
NAKATA T, 1984, 45TH S ORG SYNTH TOK, P5
[44]  
NAKATA T, 1984, 104TH ANN M PHARM SO, P280
[45]  
NAKATA T, 1982, 102ND ANN M PHARM SO, P404
[46]  
NAKATA T, 1984, 104TH ANN M PHARM SO, P279
[47]  
NAKATA T, 1982, 4TH INT C ORG SYNTH, P78
[48]   ASYMMETRIC REDUCTION BY YEASTS - FORMATION OF OPTICALLY-ACTIVE SYNTHONS HAVING 2 CHIRAL CENTERS USEFUL FOR NATURAL PRODUCT SYNTHESIS [J].
OISHI, T ;
AKITA, H .
JOURNAL OF SYNTHETIC ORGANIC CHEMISTRY JAPAN, 1983, 41 (11) :1031-1043
[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 [J].
OVERMAN, LE ;
MCCREADY, RJ .
TETRAHEDRON LETTERS, 1982, 23 (23) :2355-2358
[50]   SYNTHESIS AND MOLECULAR-STRUCTURE OF THE NIOBOCENE-CARBONYLHYDRIDE ADDUCT TO BIS-(TETRAHYDROBORATE)-ZINC [J].
PORAIKOSHITS, MA ;
ANTSYSHKINA, AS ;
PASYNSKII, AA ;
SADIKOV, GG ;
SKRIPKIN, YV ;
OSTRIKOVA, VN .
INORGANICA CHIMICA ACTA, 1979, 34 (02) :L285-L287
123456