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Title: Asymmetric Michael addition of gamma,gamma-disubstituted alpha,beta-unsaturated aldehydes to nitroolefins via dienamine catalysis. Author: Han B, Xiao YC, He ZQ, Chen YC. Journal: Org Lett; 2009 Oct 15; 11(20):4660-3. PubMed ID: 19754072. Abstract: The first chemo- and alpha-regioselective asymmetric Michael addition of gamma,gamma-disubstituted alpha,beta-unsaturated aldehydes to nitroolefins has been presented in excellent diastereo- and enantioselectivities (dr up to >99:1, 93-96% ee) via dienamine catalysis. The Michael adducts have been efficiently converted to a number of optically pure cyclic frameworks with versatile scaffold diversity.[Abstract] [Full Text] [Related] [New Search]