Preparation and assignment of configuration of 1-benzoyl- (2S)-tert-butyl-3-methyl-perhydropyrimidin-4-one. Useful starting material for the enantioselective synthesis of α-substituted β-amino acids-Reference-Cited by-同舟云学术

Preparation and assignment of configuration of 1-benzoyl- (2S)-tert-butyl-3-methyl-perhydropyrimidin-4-one. Useful starting material for the enantioselective synthesis of α-substituted β-amino acids

Published:1992-06 Issue:6 Volume:3 Page:723-726
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Juaristi Eusebio,Quintana Delia

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference17 articles.

1. Enantioselective synthesis of .beta.-amino acids. 2. Preparation of the like stereoisomers of 2-methyl- and 2-benzyl-3-aminobutanoic acid

2. Diastereoselektive Alkylierung von 3-Aminobutansäure in der 2-Stellung

3. General synthesis of enantiomerically pure β-amino acids

4. Assignment of the absolute configuration to winterstein's acid, R-3-dimethylamino-3-phenyl propionic acid, by the asymmetric synthesis of homochiral (S)-(+)-ethyl 3-dimetylamino-3-phenyl propionate

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