Hydrolase-catalyzed Michael addition of 1,3-dicarbonyl compounds to α,β-unsaturated compounds in organic solvent
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Jianming Xu | Xianfu Lin | Jianming Xu | Xianfu Lin | Qi Wu | Qi Wu | Fu Zhang | Qing‐Yi Zhang | Fu Zhang | Qing-yi Zhang
[1] Xianfu Lin,et al. Promiscuous zinc-dependent acylase-mediated carbon-carbon bond formation in organic media. , 2007, Chemical communications.
[2] A. Ghanem. Trends in lipase-catalyzed asymmetric access to enantiomerically pure/enriched compounds , 2007 .
[3] M. Reetz. Directed Evolution of Enantioselective Enzymes as Catalysts for Organic Synthesis , 2006 .
[4] Xianfu Lin,et al. Hydrolase-catalyzed Michael addition of imidazoles to acrylic monomers in organic medium. , 2006, Journal of biotechnology.
[5] K. Hult,et al. Fast carbon-carbon bond formation by a promiscuous lipase. , 2005, Journal of the American Chemical Society.
[6] V. Gotor‐Fernández,et al. Study of the Chemoselectivity in the Aminolysis Reaction of Methyl Acrylate Catalysed by Lipase B from Candida antarctica , 2005 .
[7] U. Bornscheuer,et al. Catalytic promiscuity in biocatalysis: using old enzymes to form new bonds and follow new pathways. , 2004, Angewandte Chemie.
[8] I. Alfonso,et al. Lipase catalysed Michael addition of secondary amines to acrylonitrile. , 2004, Chemical communications.
[9] Xianfu Lin,et al. Michael addition of imidazole with acrylates catalyzed by alkaline protease from Bacillus subtilis in organic media , 2004, Biotechnology Letters.
[10] Ivan Rayment,et al. Evolution of enzymatic activity in the enolase superfamily: functional studies of the promiscuous o-succinylbenzoate synthase from Amycolatopsis. , 2004, Biochemistry.
[11] W. Johnson,et al. The 4-oxalocrotonate tautomerase- and YwhB-catalyzed hydration of 3E-haloacrylates: implications for the evolution of new enzymatic activities. , 2003, Journal of the American Chemical Society.
[12] L. Fadini,et al. Ni(II) complexes containing chiral tridentate phosphines as new catalysts for the hydroamination of activated olefins. , 2003, Chemical communications.
[13] A. Volonterio,et al. Highly stereoselective tandem aza-Michael addition-enolate protonation to form partially modified retropeptide mimetics incorporating a trifluoroalanine surrogate. , 2003, Angewandte Chemie.
[14] J. Snyder,et al. Diastereoselective addition of chlorotitanium enolate of N-acyl thiazolidinethione to O-methyl oximes: A novel, stereoselective synthesis of α, β-disubstituted β-amino carbonyl compounds via chiral auxiliary mediated azetine formation , 2003 .
[15] M. Snapper,et al. Multiple component reactions: an efficient nickel-catalyzed Reformatsky-type reaction and its application in the parallel synthesis of beta-amino carbonyl libraries. , 2003, The Journal of organic chemistry.
[16] D. Herschlag,et al. SULFATASE ACTIVITY OF E. COLI ALKALINE PHOSPHATASE DEMONSTRATES A FUNCTIONAL LINK TO ARYLSULFATASES, AN EVOLUTIONARILY RELATED ENZYME FAMILY , 1998 .
[17] J. Christoffers. Transition-Metal Catalysis of the Michael Reaction of 1,3-Dicarbonyl Compounds and Acceptor-Activated Alkenes , 1998 .
[18] P. Perlmutter. Conjugate Addition Reactions in Organic Synthesis , 1992 .
[19] T. Kitazume,et al. Enzymes active in organic media: Synthesis of optically active trifluoromethylated compounds via asymmetric addition reactions , 1988 .
[20] Kurt Faber,et al. Biotransformations in Organic Chemistry , 1992 .
[21] T. Kitazume,et al. Synthesis of optically active trifluorinated compounds: asymmetric Michael addition with hydrolytic enzymes , 1986 .