Kinetic Resolution of Terminal Epoxides via Highly Regioselective and Enantioselective Ring Opening with TMSN3. An Efficient, Catalytic Route to 1,2-Amino Alcohols
- 1 January 1996
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 118 (31) , 7420-7421
- https://doi.org/10.1021/ja961708+
Abstract
No abstract availableThis publication has 24 references indexed in Scilit:
- Efficient Synthesis of (R)-4-((Trimethylsilyl)oxy)-2-cyclopentenone by Enantioselective Catalytic Epoxide Ring OpeningThe Journal of Organic Chemistry, 1996
- Preparation of Chiral Bisoxazolines: Observations on the Effect of SubstituentsThe Journal of Organic Chemistry, 1995
- Synthesis of Enantiomeric N-(2-Phosphonomethoxypropyl) Derivatives of Purine and Pyrimidine Bases. I. The Stepwise ApproachCollection of Czechoslovak Chemical Communications, 1995
- Catalytic Asymmetric DihydroxylationChemical Reviews, 1994
- Synthesis and Reactions of Optically Active CyanohydrinsAngewandte Chemie International Edition in English, 1994
- Catalytic Asymmetric C-C Bond-Forming Reaction Using Optically Active Rare Earth Complex.Journal of Synthetic Organic Chemistry, Japan, 1993
- The chiral pool as a source of enantioselective catalysts and auxiliariesChemical Reviews, 1992
- Basic character of rare earth metal alkoxides. Utilization in catalytic carbon-carbon bond-forming reactions and catalytic asymmetric nitroaldol reactionsJournal of the American Chemical Society, 1992
- Natural Product Syntheses Utilizing 4-Alkoxycarbonyloxazoles as b-Hydroxy-a-amino Acid SynthonsHETEROCYCLES, 1988
- Asymmetric epoxidation of allyl alcohol: efficient routes to homochiral .beta.-adrenergic blocking agentsThe Journal of Organic Chemistry, 1986