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

来源：

TETRAHEDRON | 1997年 / 53卷 / 20期

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

页码：6739 / 6746

页数：8

共 17 条

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[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
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