Enantioselective acylation of a beta-lactam intermediate in the synthesis of loracarbef using penicillin G amidase
- 1 March 1991
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 32 (13) , 1621-1622
- https://doi.org/10.1016/s0040-4039(00)74287-0
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- A new access to chiral 2-furylcarbinols by enantioselective hydrolysis with penicillin acylaseTetrahedron Letters, 1989
- Synthesis and biological evaluation of optically active 3-H-1-carbacephem compounds.CHEMICAL & PHARMACEUTICAL BULLETIN, 1989
- Substrate specificity and enantioselectivity of penicillinacylase catalyzed hydrolysis of phenacetyl esters of synthetically useful carbinolsTetrahedron, 1988
- Immobilized penicillinacylase: Application to the synthesis of the dipeptide aspartameTetrahedron Letters, 1986
- Hydrolysis of N-phenylacetyl-α-methyl-α-amino acids by benzylpenicillinacylaseCellular and Molecular Life Sciences, 1985
- Approach to the use of benzylpenicillin acylase for configurational correlations of amino compounds. 2. Hydrolysis of N-(p-aminophenylacetyl) derivatives of some chiral primary aminesThe Journal of Organic Chemistry, 1979