Synthetic Elaboration of the Side Chain of (R)-2,2-Dimethyl-3-(tert-butoxycarbonyl)-4-ethynyloxazolidine: A New Regio- and Stereoselective Strategy to δ-Functionalized β-Amino Alcohols
- 1 September 1997
- journal article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 62 (18), 6187-6192
- https://doi.org/10.1021/jo970619s
Abstract
No abstract availableThis publication has 26 references indexed in Scilit:
- Stereoselective Synthesis of (R)-(−)-2,2-Dimethyl-3-t-butoxycarbonyl-4-ethynyl-oxazolidine: a Chiral Building Block for the Synthesis of a New Class of Substituted AlkynesTetrahedron Letters, 1995
- Asymmetric Allylboration of 2-N,3-O-Isopropylidene-N-Boc-L-serinal: Diastereoselective Synthesis of the Calicheamicin .gamma.1I Amino SugarThe Journal of Organic Chemistry, 1995
- Stereoselective Epoxidation of Phe-Gly and Phe-Phe Vinyl IsosteresThe Journal of Organic Chemistry, 1994
- Preparation of enantiomerically pure protected 4-oxo .alpha.-amino acids and 3-aryl .alpha.-amino acids from serineThe Journal of Organic Chemistry, 1992
- Organometallic polysynthons: a novel strategy for selectively polyfunctionalized moleculesPublished by Walter de Gruyter GmbH ,1992
- Stereocontrolled synthesis of Ψ[CH=CH] dipeptide isosteresInternational Journal of Peptide and Protein Research, 1991
- Synthesis of chiral vinylglycinesThe Journal of Organic Chemistry, 1991
- Stannylcupration as a Highly Regio- and Stereoselective route to 2-Substituted Tributylstannyl AllylaminesSynthesis, 1991
- The Palladium‐Catalyzed Cross‐Coupling Reactions of Organotin Reagents with Organic Electrophiles [New Synthetic Methods (58)]Angewandte Chemie International Edition in English, 1986
- Rapid chromatographic technique for preparative separations with moderate resolutionThe Journal of Organic Chemistry, 1978