| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1354913 | Tetrahedron: Asymmetry | 2019 | 6 Pages |
Abstract
Formation of optically active α or γ-phenylcyclohexanone oximes (2a and 2b, c) and their esters (1a and 3b, c) by lipase mediated transesterification of the corresponding racemic esters is described. Furthermore, 2(S)-phenyl and 2,2-dimethyl-4(R)-phenylcyclohexanones (4 and 5) were prepared without any racemization.
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Masatoshi Murakata, Megumi Imai, Masafumi Tamura, Osamu Hoshino,