ω-Functionalized Esters by Enzymatic Acylation
- 1 March 1990
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 20 (5) , 679-685
- https://doi.org/10.1080/00397919008052310
Abstract
ω-halo, ω-carboxylic, ω-keto and β-hydroxy carboxylic esters of (1) were obtained by lipase-catalyzed acylation.Keywords
This publication has 3 references indexed in Scilit:
- An interesting example of complementary regioselective acylation of secondary hydroxyl groups by different lipasesTetrahedron Letters, 1989
- Asymmetric ring opening of cyclic acid anhydrides with lipase in organic solventsTetrahedron Letters, 1988
- Protease-catalyzed regioselective esterification of sugars and related compounds in anhydrous dimethylformamideJournal of the American Chemical Society, 1988