Chiral cooperativity: the nature of the diastereoselective and enantioselective step in the gold(I)-catalyzed aldol reaction utilizing chiral ferrocenylamine ligands
Enantioselective Synthesis: Steric and electronic effects of the substrates upon stereoselectivity in the gold(I)-catalyzed aldol reaction with chiral ferrocenylamine ligands, preliminary communication
作者:Antonio Togni、Stephen D. Pastor
DOI:10.1002/hlca.19890720521
日期:1989.8.9
Enantioselectivity in the gold(I)-catalyzed aldol reaction with chiral ferrocenylamine ligands is strongly dependent upon both the steric and electronic effects of the substrates. In the reaction of pyridine-2-, 3-, and 4-carbaldehydes with ethyl 2-isocyanoacetate, surprisingly and significantly different enantioselectivities were observed in the formation of the cis- and trans-dihydro-oxazoles that
Enantioselective synthesis: Catalysis of the aldol reaction by neutral gold(I)-chiral ferrocenylphosphine complexes. Crystal structure of the complex [{(η5-C5H4PPh2)(η5-C5H3(PPh2)CH(Me)N(Me)CH2CH2NMe2)Fe}2(AuCl)3] · Et2O