Asymmetric Synthesis IX1: Preparation of Chiral α-Substituted Phenethylamines
- 1 April 1987
- journal article
- research article
- Published by Taylor & Francis Ltd in Synthetic Communications
- Vol. 17 (6), 669-676
- https://doi.org/10.1080/00397918708075740
Abstract
(S)-N-methyl-α-methyl-phenethylamines 5a-d were obtai-ned in 56–62% e.e. from the chiral synthoh (-)-N-cyano-methyl-4-phenyl-1,3-oxazolidine-1.Keywords
This publication has 4 references indexed in Scilit:
- Asymmetric synthesis VIII: Biogenetically patterned approach to the chiral total synthesis of (−)-pumiliotoxin-CTetrahedron Letters, 1986
- Asymmetric synthesis IV. Preparation of chiral α-aminonitriles from a new N-cyanomethyl-1,3-oxazolidine synthonTetrahedron Letters, 1985
- Asymmetric .ALPHA.-substituted phenethylamines. V. Synthesis of chiral 1-alkyl-2-phenylethylamines via Grignard reaction of 4-phenyl-1,3-oxazolidines.CHEMICAL & PHARMACEUTICAL BULLETIN, 1985
- Nuclear magnetic resonance enantiomer regents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and .alpha.-methoxy-.alpha.-trifluoromethylphenylacetate (MTPA) estersJournal of the American Chemical Society, 1973