ENANTIOSELECTIVITY IN MICROBIAL REDUCTION OF PROCHIRAL CARBONYL GROUPS: A WIDE SCREENING TOWARD R AND S ISOMERS

DOI: 10.1016/S0957-4166(00)80043-9

Source and publish data:

Tetrahedron Asymmetry p. 243 - 246 (1991)

Update date:2022-08-16

Topics:

Authors:

Fantin, Giancarlo

Fogagnolo, Marco

Medici, Alessandro

Pedrini, Paola

Poli, Silvia

et al. et al.

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Article abstract of DOI:10.1016/S0957-4166(00)80043-9

More than fifty yeast and mould strains were tested in the reduction of 2-acylthiazoles 1-5.The possibility of obtaining R or S enantiomers with high enantioselectivities from various species and strains is described.

Full text of DOI:10.1016/S0957-4166(00)80043-9

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