A highly enantioselective hydrolysis of cis-3,5-diacetoxycyclopent-1-ene. : An enzymatic preparation of 3(R)-acetoxy-5(S)-hydroxycyclopent-1-ene.
- 31 December 1986
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 27 (11), 1255-1256
- https://doi.org/10.1016/s0040-4039(00)84231-8
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Immobilized porcine liver esterase: a convenient reagent for the preparation of chiral building blocks.Tetrahedron Letters, 1985
- Enzymatic hydrolysis of prochiral
cis-1,4-diacyl-2-cyc-lopentenediols: preparation of (1 S,4 R)-and (1 R,4 S)-4-hydroxy-2-cyclopentenylderivatives, versatile building blocks for cyclopentanoid natural products. Tetrahedron Letters, 1984 - Bifunctional chiral synthons via biochemical methods. III. Optical purity enhancement in enzymic asymmetric catalysisJournal of the American Chemical Society, 1984
- 4‐Oxo‐2‐cyclopentenyl Acetate—A Synthetic IntermediateAngewandte Chemie International Edition in English, 1982
- Prostaglandin chemistry—IVTetrahedron, 1976
- Prostaglandin chemistry—VTetrahedron, 1976
- .alpha.-Methoxy-.alpha.-trifluoromethylphenylacetic acid, a versatile reagent for the determination of enantiomeric composition of alcohols and aminesThe Journal of Organic Chemistry, 1969