| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10579552 | Tetrahedron: Asymmetry | 2010 | 8 Pages |
Abstract
Racemic alkyl-2-hydroxy-4-arylbut-3-ynoates were deracemized to the (S)-alkyl-2-hydroxy-4-arylbut-3-ynoates in excellent enantiomeric excesses (up to >99%) and good isolated yields (up to 81%) with the biocatalyst Candida parapsilosis ATCC 7330. The absolute configuration of the resulting enantiomer was assigned by 1H NMR using Mosher's method.
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Physical Sciences and Engineering
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Authors
Thangavel Saravanan, Anju Chadha,