Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1349421 | Tetrahedron: Asymmetry | 2005 | 6 Pages |
Abstract
Saccharomyces cerevisiae, strain DBM 2115, was successfully employed in the reduction of the separated Z- and E-isomers of ethyl 4-[(2-oxocyclohexyl)methyl]phenoxy-3-methyl-2-butenoates 1 and 2, in order to prepare the (1S,2S)- and (1R,2S)-enantiomers of the corresponding ethyl 4-[(2-hydroxycyclohexyl)methyl]phenoxy-3-methyl-2-butenoates 3-6. The products were obtained with the required absolute configuration: (1S,2S)-3 (ee = 98%; yield 48%), (1R,2S)-4 (ee = >99%; yield 45%), (1S,2S)-5 (ee = 98.5%; yield 47%), and (1R,2S)-6 (ee = >99%; chemical yield 44%).
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
ZdenÄk Wimmer, David Å aman, Marie Zarevúcka, Martina Wimmerová,