作者: A. Corma , M. Iglesias , C. del Pino , F. Sánchez
DOI: 10.1039/C39910001253
关键词:
摘要: Rh-complexes with N-based chiral ligands, when anchored on a modified USY-zeolite which contains profuse supermicropores, produce remarkable increase of enantioselectivity (>95%) in the hydrogenation N-acyldehydrophenylalanine derivatives and represent truly heterogeneous counterpart homogeneous organometallic catalysts.