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Cyclophane chirality transfer

Much related work has occxured based on organized catalysis in natural and synthetic macrocycles, polymers, and modified surfaces, which can only be hinted at briefly in such a review. We highlight Lehn s application of crown-ethers (83) and (84) in the catalysis of hydrolysis of chiral dipeptide esters (S R up to 50 1) and hydride transfer to ketones, respectively, Knowles s successful preparation of specifically substituted a-cyclodextrins (85) and their involvement in phosphate ester hydrolysis, and Murakami s syntheses of catalytically active p-cyclophanes. " The long-standing contribution of... [Pg.216]


See other pages where Cyclophane chirality transfer is mentioned: [Pg.123]    [Pg.123]    [Pg.207]    [Pg.261]    [Pg.62]    [Pg.359]    [Pg.62]    [Pg.391]    [Pg.144]    [Pg.188]    [Pg.91]    [Pg.357]    [Pg.72]    [Pg.104]    [Pg.476]    [Pg.91]    [Pg.363]    [Pg.456]    [Pg.188]   
See also in sourсe #XX -- [ Pg.261 ]




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