Synthesis of versatile intermediates for cyclopentanoid natural products via enantioselective deprotonation of substituted cyclopentene oxide
- 17 April 1995
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 36 (16) , 2847-2850
- https://doi.org/10.1016/0040-4039(95)00364-i
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Enantioselective Deprotonation of Cyclohexene Oxide to (R)-2-Cyclohexen-1-olSynthetic Communications, 1994
- Dilithiated aminoalcohols as homochiral basesJournal of the Chemical Society, Chemical Communications, 1993
- A Novel Asymmetric Synthesis of Chiral Cyclopentanoid Building Blocks by the Use of Chiral Lithium AmideBulletin of the Chemical Society of Japan, 1990
- Asymmetric Trasformation of Symmetrical Epoxides to Allylic Alcohols by Lithium (S)-2-(N,N-Disubstituted aminomethyl)pyrrolidideBulletin of the Chemical Society of Japan, 1990
- Non-enzymatic asymmetric transformations involving symmetrical bifunctional compoundsChemical Society Reviews, 1990
- Racemization-free and efficient peptide synthesis by the carbodiimide method using 1-hydroxybenzotriazole and copper(II) chloride simultaneously as additivesJournal of the Chemical Society, Chemical Communications, 1988
- An Asymmetric Transformation of Symmetrical Epoxides to Both Enantiomers of Allylic Alcohols by Chiral Lithium AmidesChemistry Letters, 1987
- AN ASYMMETRIC TRANSFORMATION OF CYCLOHEXENE OXIDE TO (S)-2-CYCLOHEXEN-1-OL BY CHIRAL LITHIUM AMIDESChemistry Letters, 1984
- 4‐Oxo‐2‐cyclopentenyl Acetate—A Synthetic IntermediateAngewandte Chemie International Edition in English, 1982
- Asymmetric induction. 3. Enantioselective deprotonation by chiral lithium amide basesThe Journal of Organic Chemistry, 1980