Author:
Hodge Philip,Kell Roger J.,Ma Jianbiao,Morris Hugh
Abstract
Polystyrene beads containing
N-alkyl-α,α-diphenyl-L-prolinol moieties (7)
linked to the support via a long N-alkyl group, which
also serves as a spacer chain, have been prepared. When used to catalyse the
reactions of aldehydes with diethylzinc at 10 mole % in toluene at
20°C they afford the expected alcohols in 59–83% e.e. Where
comparisons can be made with the results obtained with
N-methyl-α,α-diphenyl-L-prolinol (3), the
PS(polymer- supported) catalysts afford lower percentage e.e. values. Evidence
is provided that this is due in part to the presence of the spacer chain, and
in part because with the PScatalysts not all the catalyst sites are readily
accessible. The latter means that the PScatalysts cannot compete
satisfactorily with the uncatalysed reactions between aldehydes and
diethylzinc which produce racemates. Thus, if higher percentage e.e. values
are to be obtained in future with PS α,α-diphenyl-L-prolinol
derivatives, the catalyst sites will most likely need to be bound to the
polymer via the phenyl groups or substituents on the five-membered ring.
Cited by
9 articles.
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