A Novel Asymmetric Synthesis of Chiral Cyclopentanoid Building Blocks by the Use of Chiral Lithium Amide
- 1 May 1990
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 63 (5) , 1402-1408
- https://doi.org/10.1246/bcsj.63.1402
Abstract
No abstract availableThis publication has 24 references indexed in Scilit:
- Asymmetric Trasformation of Symmetrical Epoxides to Allylic Alcohols by Lithium (S)-2-(N,N-Disubstituted aminomethyl)pyrrolidideBulletin of the Chemical Society of Japan, 1990
- A highly enantioselective hydrolysis of -3,5-diacetoxycyclopent-1-ene.Tetrahedron Letters, 1986
- Immobilized porcine liver esterase: a convenient reagent for the preparation of chiral building blocks.Tetrahedron Letters, 1985
- Acylation énantiosélective d'un diol méso : le cis-cyclopentène-2 diol-1,4Tetrahedron Letters, 1985
- Enzymatic hydrolysis of prochiral -1,4-diacyl-2-cyc-lopentenediols: preparation of (1,4)-and (1,4)-4-hydroxy-2-cyclopentenylderivatives, versatile building blocks for cyclopentanoid natural products.Tetrahedron Letters, 1984
- Prostaglandin‐Synthesen durch Dreikomponenten‐KupplungAngewandte Chemie, 1984
- Bifunctional chiral synthons via biochemical methods. III. Optical purity enhancement in enzymic asymmetric catalysisJournal of the American Chemical Society, 1984
- 4‐Oxo‐2‐cyclopentenylacetat — ein SynthesebausteinAngewandte Chemie, 1982
- Stereochemical studies—LVIITetrahedron, 1980
- Asymmetric synthesis of prostaglandin intermediatesJournal of the American Chemical Society, 1973