Lipase Catalysed Preparation of Optically Active α-Phenylethanol and the Related Substrates under Solvent free Condition †
暂无分享,去创建一个
[1] K. S. Bisht,et al. Lipase-catalyzed solvent-free kinetic resolution of substituted racemic ε-caprolactones , 2002 .
[2] M. Mamaghani. Enzymatic kinetic resolution of aromatic substituted norbornene mono-esters using pig's liver esterase , 2002 .
[3] M. Nair,et al. Lipase catalyzed kinetic resolution of aryl β-hydroxy ketones , 2000 .
[4] V. Gotor. Non-conventional hydrolase chemistry: amide and carbamate bond formation catalyzed by lipases. , 1999, Bioorganic & medicinal chemistry.
[5] J. Metzger. Solvent-Free Organic Syntheses. , 1998, Angewandte Chemie.
[6] Keiji Hirose,et al. Enantioselective acylation of alcohols catalyzed by lipase QL from Alcaligenes sp.: A predictive active site model for lipase QL to identify the faster reacting enantiomer of an alcohol in this acylation , 1996 .
[7] A. Banerji,et al. Biotransformations with Rhizopus arrhizus: Preparation of the enantiomers of 1-phenylethanol and 1-(fo-, m- and p-methoxyphenyl)ethanols , 1995 .
[8] G. Asensio,et al. Influence of structural factors and enzyme type on the reactivity and enantioselectivity of the enzymatic esterification of bicyclic meso dialcohols , 1992 .
[9] R. Csuk,et al. Baker's yeast mediated transformations in organic chemistry , 1991 .
[10] Tamio Hayashi,et al. Catalytic asymmetric hydroboration of styrenes , 1989 .
[11] M. Schneider,et al. Enzymic preparation of enantiomerically pure secondary alcohols. Ester synthesis by irreversible acyl transfer using a highly selective ester hydrolase from Pseudomonas sp.; an attractive alternative to ester hydrolysis , 1988 .