Enantiomers of ring-substituted 2-amino-1-phenylethanols by Pseudomonas cepacia lipase
- 30 September 1995
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 6 (9) , 2281-2286
- https://doi.org/10.1016/0957-4166(95)00303-7
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Combination of the lipase-catalysed resolution with the Mitsunobu esterification in one potTetrahedron: Asymmetry, 1995
- Baker’s Yeast Reduction of α-(Acylamino)acetophenones and Lipase Catalyzed Resolution of 2-Acylamino-1-arylethanolsBulletin of the Chemical Society of Japan, 1993
- Enzymatic acylation in the resolution of methyl threo-2-hydroxy-3-(4-methoxyphenyl)-3-(2-X-phenylthio)propionates in organic solventsJournal of the Chemical Society, Perkin Transactions 1, 1993
- Lipase catalysis in the optical resolution of 2-amino-1-phenylethanol derivativesJournal of the Chemical Society, Perkin Transactions 1, 1992
- Studies on the Chemo- and Enantio-selectivity of the Enzymatic Monoacylations of Amino Alcohols.Acta Chemica Scandinavica, 1992
- Chirality in α- and β-adrenoceptor agonists and antagonistsTetrahedron, 1991
- Lipase-ctalysed kinetic resolution of N,O-diacetyl-2-amino-1-butanol in diisopropyl ether.Tetrahedron: Asymmetry, 1990
- Enantioselective acylation of amino alcohols by porcine pancreatic lipaseJournal of the Chemical Society, Chemical Communications, 1988
- Lipase-catalyzed resolution of chiral 2-amino 1-alcoholsThe Journal of Organic Chemistry, 1987