Substrate specificity and enantioselectivity of penicillinacylase catalyzed hydrolysis of phenacetyl esters of synthetically useful carbinols
- 1 January 1988
- journal article
- research article
- Published by Elsevier in Tetrahedron
- Vol. 44 (9) , 2575-2582
- https://doi.org/10.1016/s0040-4020(01)81708-7
Abstract
No abstract availableThis publication has 23 references indexed in Scilit:
- Stereochemistry and synthetic applications of the products of yeast reduction of 3-hydroxy-3-methyl-5-phenylpent-4-en-2-oneThe Journal of Organic Chemistry, 1987
- Penicillinacylase and α-chymotrypsin catalysed hydrolysis of phenylacetate and phenylpropionate esters of 2,2-dimethyl-1,3-dioxolane-4-methanolsJournal of the Chemical Society, Chemical Communications, 1987
- Enzymes in organic synthesis. 35. Stereoselective pig liver esterase catalyzed hydrolyses of 3-substituted glutarate diesters. Optimization of enantiomeric excess via reaction conditions controlThe Journal of Organic Chemistry, 1986
- On the steric course of bakers' yeast reduction of .alpha.-hydroxy ketonesThe Journal of Organic Chemistry, 1984
- Improved synthesis and absolute configuration of (+)- and (-)-2,2,4-trimethyl-1,3-dioxolane-4-carboxaldehydeThe Journal of Organic Chemistry, 1983
- Optisch aktive C5‐Bausteine zur Synthese von natürlich vorkommenden TerpenenHelvetica Chimica Acta, 1983
- Racematspaltung und Bestimmung der absoluten Konfiguration von 2, 6‐disubstituierten Bicyclo [3.3.1]nonanenHelvetica Chimica Acta, 1978
- Immobilized enzyme reaction stability: Attrition of the support materialBiotechnology & Bioengineering, 1974
- Properties of the Penicillin Deacylase Enzyme of Escherichia coliNature, 1964
- 19. The (+) and (–)γ-phenyl-α-methylallyl alcoholsJournal of the Chemical Society, 1936