Tetrahedron Asymmetry p. 149 - 153 (1997)
Update date:2022-08-16
Topics:
Bailey, David J.
O'Hagan, David
Tavasli, Mustafa
A three step synthesis of (S)-2(diphenylmethyl)pyrrolidine 4 is described which allows its preparation on a large scale. The C2 symmetric diamines 5 and 6 have been prepared from 4 and are attractive as potential ligands for asymmetric transformations. Pyrrolidine 4 has been assessed as a chiral solvating agent for the NMR analysis of chiral compounds. It emerges as a good CSA for carboxylic acids and some secondary alcohols.
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