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New multifunctional chiral phosphines and BINOL derivatives co-catalyzed enantioselective aza-Morita–Baylis–Hillman reaction of 5,5-disubstituted cyclopent-2-enone and N-sulfonated imines†
Yuan-Liang Yang,Yin Wei
Organic & Biomolecular Chemistry Pub Date : 07/24/2012 00:00:00 , DOI:10.1039/C2OB25932J
Abstract

New multifunctional chiral phosphine (phosphine-amide type) LB8 and BINOL derivative co-catalyzed asymmetric aza-MBH reaction of 5,5-disubstituted cyclopent-2-enones 1 with N-sulfonated imines 2 afforded the corresponding optically active adducts 3 in good to outstanding yields with moderate to good ee's under mild conditions. The steric hindrance environment of BINOL derivatives as well as the nucleophilicity of the phosphorus center and the acidity of free OH which could significantly affect the stereochemical and chemical outcomes had been discussed, indicating the co-catalyzed system is very important to this particular asymmetric aza-MBH reaction.

Graphical abstract: New multifunctional chiral phosphines and BINOL derivatives co-catalyzed enantioselective aza-Morita–Baylis–Hillman reaction of 5,5-disubstituted cyclopent-2-enone and N-sulfonated imines
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