1225301-97-2Relevant academic research and scientific papers
Sequential use of regio- and stereoselective lipases for the efficient kinetic resolution of racemic 1-(5-phenylfuran-2-yl)ethane-1,2-diols
Bencze, Laszlo Csaba,Paizs, Csaba,Toa, Monica Ioana,Irimie, Florin Dan
scheme or table, p. 675 - 683 (2011/07/09)
Possible routes for the enzymatic transformation of various substituted 1-(5-phenylfuran-2-yl)ethane-1,2-diols and their mono- and diacetylated counterparts were studied. Combining the regioselectivity of LPS mediated acylation of the starting racemic dio
Substituent effects on the stereochemical outcome of the baker's yeast-mediated biotransformation of α-hydroxy- and α-acetoxymethyl-5-phenylfuran-2-yl-ethanones
Bencze, Laszlo Csaba,Paizs, Csaba,Tosa, Monica Ioana,Irimie, Florin Dan
experimental part, p. 356 - 364 (2010/06/16)
In this Letter the baker's yeast-mediated biotransformation of variously substituted α-hydroxy- and α-acetoxymethyl-5-phenylfuran-2-yl-ethanones is described. The stereochemical outcome of the reactions was strongly influenced by the nature of the substituents on the phenyl ring.
