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Cinchona-promoted asymmetric nucleophilic 1,2-addition reactions

The asymmetric conjugate additions with thiol nucleophiles was further expanded to 2-mercaptobenzaldehydes [98]. Wang had previously developed a domino Michael-aldol reaction promoted by Cinchona alkaloids, and now illustrated the utihty of cyclohexane-diamine bifunctionalized catalysts for the domino... [Pg.176]

See other pages where Cinchona-promoted asymmetric nucleophilic 1,2-addition reactions is mentioned: [Pg.249]    [Pg.70]    [Pg.173]    [Pg.33]    [Pg.48]    [Pg.58]    [Pg.318]    [Pg.323]    [Pg.318]    [Pg.323]    [Pg.5]    [Pg.193]    [Pg.4]    [Pg.266]    [Pg.862]    [Pg.862]   
See also in sourсe #XX -- [ Pg.484 ]



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Addition reactions asymmetric

Addition reactions nucleophilic

Asymmetric addition

Cinchona

Cinchona-promoted asymmetric

Cinchona-promoted asymmetric reactions

Nucleophile addition reactions

Nucleophiles addition reactions

Promoters reaction

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