Highly Enantioselective Hydrogenative Desymmetrization of Bicyclic Imides Leading to Multiply Functionalized Chiral Cyclic Compounds

Highly enantioselective hydrogenative desymmetrization of bicyclic imides has been developed with chiral Cp*Ru(PN) catalysts. The present hydrogenation directly provides stereochemically well-defined cyclic compounds with excellent enantiomeric exessses, which might otherwise require a detour to rea...

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Veröffentlicht in:Journal of the American Chemical Society 2010-08, Vol.132 (33), p.11414-11415
Hauptverfasser: Ito, Masato, Kobayashi, Chika, Himizu, Akio, Ikariya, Takao
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container_end_page 11415
container_issue 33
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container_title Journal of the American Chemical Society
container_volume 132
creator Ito, Masato
Kobayashi, Chika
Himizu, Akio
Ikariya, Takao
description Highly enantioselective hydrogenative desymmetrization of bicyclic imides has been developed with chiral Cp*Ru(PN) catalysts. The present hydrogenation directly provides stereochemically well-defined cyclic compounds with excellent enantiomeric exessses, which might otherwise require a detour to reach.
doi_str_mv 10.1021/ja105048c
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subjects Bridged Bicyclo Compounds, Heterocyclic - chemical synthesis
Bridged Bicyclo Compounds, Heterocyclic - chemistry
Hydrogenation
Imides - chemical synthesis
Imides - chemistry
Molecular Structure
Stereoisomerism
title Highly Enantioselective Hydrogenative Desymmetrization of Bicyclic Imides Leading to Multiply Functionalized Chiral Cyclic Compounds
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