Long-distance control in stereoselective reduction of 3-[3-(4?-bromo[1,1?-biphenyl]-4-yl)-3-keto-1-phenylpropyl]-4-hydroxy-2H-1-benzopyran-2-one: Relative configuration of prevailing diastereomer and absolute configuration of its enantiomers-Reference-Cited by-同舟云学术

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Long-distance control in stereoselective reduction of 3-[3-(4?-bromo[1,1?-biphenyl]-4-yl)-3-keto-1-phenylpropyl]-4-hydroxy-2H-1-benzopyran-2-one: Relative configuration of prevailing diastereomer and absolute configuration of its enantiomers

Published:1997 Issue:5-6 Volume:9 Page:512-522
ISSN:0899-0042
Container-title:Chirality
language:en
Short-container-title:Chirality

Author:

Avdagi? Amir,Cotarca Livius,Hamer?ak Zdenko,Holl�si Miklos,Majer Zsuzsa,Ljubovi? Edina,?uste Andreja,?unji? Vitomir

Publisher

Wiley

Subject

Organic Chemistry,Spectroscopy,Drug Discovery,Pharmacology,Catalysis,Analytical Chemistry

Reference32 articles.

1. Rodenticides. In: Uhlmann's Encyclopedia of Industrial Chemistry. Vol. A23. VCH Publishers, 1993 211-220.

2. Biochemical basis of warfarin and bromadiolone resistance in the house mouse, Mus musculus domesticus

3. A convenient route for the synthesis of s,s-and R,R-warfarin alcohols

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. First evidence of widespread anticoagulant rodenticide exposure of the Eurasian otter (Lutra lutra) in Germany;Science of The Total Environment;2024-01

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