A new access to chiral 2-furylcarbinols by enantioselective hydrolysis with penicillin acylase
- 31 December 1989
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 30 (23), 3057-3058
- https://doi.org/10.1016/s0040-4039(00)99401-2
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- Chemoenzymic synthesis of chiral furan derivatives: useful building blocks for optically active structuresThe Journal of Organic Chemistry, 1988
- Molecular complex evaluation. A simultaneous assay of binding using substrate mixturesThe Journal of Organic Chemistry, 1988
- Stereoselective synthesis of (+)-Prelog-Djerassi lactone from furanoid intermediatesThe Journal of Organic Chemistry, 1987
- The aza-achmatowicz rearrangement: A route to useful building blocks for N- containing structuresTetrahedron Letters, 1986
- Synthesis of both the enantiomers of the heterocyclic pheromones isolated from the male swift moth lTetrahedron, 1986
- The absolute configuration of P-1894B, a potent prolyl hydroxylase inhibitor.CHEMICAL & PHARMACEUTICAL BULLETIN, 1984
- [54b] Penicillin acylase (bacterial)Methods in Enzymology, 1975
- ABSOLUTE CONFIGURATIONS OF TWO SUGARS OF ANTIBIOTIC B-58941Chemistry Letters, 1973
- Oxidation of furans - I. synthesis of 6-hydroxy-2H-pyran-3(6H)-onesTetrahedron Letters, 1972
- Synthesis of methyl 2,3-dideoxy-DL-alk-2-enopyranosides from furan compoundsTetrahedron, 1971