Stereoselective synthesis of 2-aryloxy esters: An asymmetric approach to fluoxetine, tomoxetine and nisoxetine

被引:54
作者
Devine, PN
Heid, RM
Tschaen, DM
机构
[1] Department of Process Research, Merck Research Laboratories Division, Merck and Co., Inc., Rahway, NJ 07065
关键词
D O I
10.1016/S0040-4020(97)00325-6
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
[No abstract available]
引用
收藏
页码:6739 / 6746
页数:8
相关论文
共 17 条
[2]   CHEMOENZYMATIC SYNTHESIS OF BOTH ENANTIOMERS OF FLUOXETINE [J].
CHENEVERT, R ;
FORTIER, G .
CHEMISTRY LETTERS, 1991, (09) :1603-1606
[3]  
CHOVINARD GA, 1986, DRUGS FUTURE, V11, P134
[4]  
CHOVINARD GA, 1985, J CLIN PSYCHIAT, V46, P32
[5]   ENANTIOSELECTIVE AND PRACTICAL SYNTHESES OF R-FLUOXETINE AND S-FLUOXETINE [J].
COREY, EJ ;
REICHARD, GA .
TETRAHEDRON LETTERS, 1989, 30 (39) :5207-5210
[6]   Stereoselective synthesis of 2-aryloxy acids from lactamide derived esters of racemic alpha-halo carboxylic acids. [J].
Devine, PN ;
Dolling, UH ;
Heid, RM ;
Tschaen, DM .
TETRAHEDRON LETTERS, 1996, 37 (16) :2683-2686
[7]   ASYMMETRIC-SYNTHESIS OF BOTH ENANTIOMERS OF TOMOXETINE AND FLUOXETINE - SELECTIVE REDUCTION OF 2,3-EPOXYCINNAMYL ALCOHOL WITH RED-AL [J].
GAO, Y ;
SHARPLESS, KB .
JOURNAL OF ORGANIC CHEMISTRY, 1988, 53 (17) :4081-4084
[8]  
GU JX, 1993, TETRAHEDRON, V49, P5805
[9]   NOVEL SYNTHESES OF THE CARBAPENEM KEY INTERMEDIATES, (3R,4R)-4-ACETOXY-3-[(R)-1-(TERT-BUTYLDIMETHYLSILYLOXY)ETHYL]-2-AZETIDINONE AND (3S,4R)-3-[(R)-1-(TERT-BUTYLDIMETHYLSILYLOXY)ETHYL]-4-CARBOXYMETHYL-2-AZETIDINONE, FROM (S)-ETHYL LACTATE [J].
ITO, Y ;
KOBAYASHI, Y ;
KAWABATA, T ;
TAKASE, M ;
TERASHIMA, S .
TETRAHEDRON, 1989, 45 (18) :5767-5790
[10]   A CONVENIENT METHOD FOR PREPARING ENANTIOMERICALLY PURE NORFLUOXETINE, FLUOXETINE AND TOMOXETINE [J].
KOENIG, TM ;
MITCHELL, D .
TETRAHEDRON LETTERS, 1994, 35 (09) :1339-1342