Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/24085
Title: Chiral pyrrolidine derivatives as catalysts in the enantioselective addition of diethylzinc to aldehydes
Authors: Yang, X
Shen, J
Da, C
Wang, R
Choi, MCK
Yang, L
Wong, KY 
Issue Date: 1999
Source: Tetrahedron asymmetry, 1999, v. 10, no. 1, p. 133-138 How to cite?
Journal: Tetrahedron Asymmetry 
Abstract: A series of pyrrolidine derivatives with β-amino alcohol moieties prepared from (S)-proline were found to catalyze the enantioselective addition of diethylzinc to aldehydes to yield optically active secondary alcohols with high enantioselectivities. A mechanism accounting for the configurational change with the bulkiness of chiral ligands is proposed.
URI: http://hdl.handle.net/10397/24085
ISSN: 0957-4166
DOI: 10.1016/S0957-4166(98)00497-2
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