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Synthesis of a Racemic Ester and Its Lipase-Catalyzed Kinetic Resolution

✍ Scribed by Stetca, Delia; Arends, Isabel W. C. E.; Hanefeld, Ulf


Book ID
120502389
Publisher
American Chemical Society
Year
2002
Tongue
English
Weight
69 KB
Volume
79
Category
Article
ISSN
0021-9584

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πŸ“œ SIMILAR VOLUMES


Lipase-catalyzed kinetic resolution of r
✍ Kosei Shioji; Ayako Matsuo; Kentaro Okuma; Kaoru Nakamura; Atsuyoshi Ohno πŸ“‚ Article πŸ“… 2000 πŸ› Elsevier Science 🌐 French βš– 60 KB

Optically active 3-, 4-, 5-, or 6-methyl substituted seven-membered lactones were prepared by Candida antarctica lipase (CAL)-catalyzed kinetic resolution of the racemic lactones. Among these lactones, only in the case of 5-methylhexanolide (R)-isomer reacts faster than the other enantiomer, while t

Kinetic resolution of amino acid esters
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Racemic amino acids were resolved by lipase via hydrolysis of their esters. Lipases (Pseudomonas lipase from Amano PS, Rhizopus lipase from Serva, and porcine pancrease lipase from Sigma) could selectively hydrolyze the L-amino acid esters in aqueous solution with high reactivities and selectivities