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Enantioselective reduction Lewis-acid catalysis

A more versatile method to use organic polymers in enantioselective catalysis is to employ these as catalytic supports for chiral ligands. This approach has been primarily applied in reactions as asymmetric hydrogenation of prochiral alkenes, asymmetric reduction of ketone and 1,2-additions to carbonyl groups. Later work has included additional studies dealing with Lewis acid-catalyzed Diels-Alder reactions, asymmetric epoxidation, and asymmetric dihydroxylation reactions. Enantioselective catalysis using polymer-supported catalysts is covered rather recently in a review by Bergbreiter [257],... [Pg.519]


See other pages where Enantioselective reduction Lewis-acid catalysis is mentioned: [Pg.40]    [Pg.97]    [Pg.157]    [Pg.113]    [Pg.313]    [Pg.66]    [Pg.563]    [Pg.4]    [Pg.195]    [Pg.958]    [Pg.958]   
See also in sourсe #XX -- [ Pg.164 , Pg.165 , Pg.166 , Pg.167 , Pg.168 , Pg.169 ]




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Enantioselective catalysis

Lewis acid reduction

Lewis acids acid catalysis

Lewis acids, catalysis

Lewis catalysis

Reduction enantioselective

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