A highly enantioselective synthesis of cyclic α-amino acids involving a one-pot, single catalyst, tandem hydrogenation–hydroformylation sequence†
Euneace Teoh,Eva M. Campi,W. Roy Jackson,Andrea J. Robinson
Chemical Communications Pub Date : 04/04/2002 00:00:00 , DOI:10.1039/B200374K
Abstract

Tandem enantioselective hydrogenation followed by a hydroformylation–cyclisation sequence leading to cyclic α-amino acids with ee’s >95% can be achieved in a single pot, one catalyst system by successive reactions of prochiral dienamide esters with H2 followed by H2/CO using Rh(I)-DuPHOS.

Graphical abstract: A highly enantioselective synthesis of cyclic α-amino acids involving a one-pot, single catalyst, tandem hydrogenation–hydroformylation sequence