
Tetrahedron Asymmetry p. 60 - 66 (2008)
Update date:2022-07-30
Topics:
Takahashi, Miyuki
Haraguchi, Naoki
Itsuno, Shinichi
Polymer-supported chiral 1,2-diamines were prepared by two methods including (1) chemical modification of a Merrifield-type resin with a chiral 1,2-diamine and (2) polymerization of a 1,2-diamine monomer. The polymeric complex formed by the polymer-supported 1,2-diamine and RuCl2-BINAP was used for the asymmetric hydrogenation of aromatic ketones to afford the corresponding secondary alcohols in quantitative yields with high enantioselectivities up to 99% ee in the asymmetric hydrogenation. The polymeric catalyst could be reused many times without any loss of activity or enantioselectivity.
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(2008)Doi:10.1007/BF00637279
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()Doi:10.1016/j.bmcl.2007.12.030
(2008)Doi:10.1021/om700584m
(2008)