Synthesis of Enantiopure N-and C-Protected homo-β-Amino Acids by Direct Homologation of α-Amino Acids ¶

Tetrahedron

Volumn 51, Issue 45, 1995, Pages 12337-12350

  Caputo, Romualdo ^a   Cassano, Ersilia ^a   Longobardo, Luigi ^a   Palumbo, Giovanni ^a  

^a UNIVERSITY OF NAPLES FEDERICO II   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID DERIVATIVE; BETA AMINO ACID;

ARTICLE; DRUG PURITY; DRUG SYNTHESIS; ENANTIOMER; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; METHODOLOGY; PRIORITY JOURNAL; REACTION ANALYSIS;

EID: 0028826307     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4020(95)00778-7     Document Type: Article

References (39)

1. 2H group of an α-amino acid
2. A method for the synthesis of alkynyl phenyl sulfides from alkynyltrimethylsilanes. A novel, efficient synthesis of the thienamycin intermediate from 3(R)-hydroxybutyric acid
3. A Convenient One-Pot Conversion ofN-Protected Amino Acids and Peptides into Alcohols
4. Novel reagent system for converting a hydroxy-group into an iodo-group in carbohydrates with inversion of configuration. Part 2
5. Preparation and C-Alkylation of Enantiomerically PureS-Phenyl Aziridinecarbothioates. On the Structure of Small-Ring Ester Lithium Enolates
6. Synthesis of protected amino alcohols: a comparative study
7. A new method for the deoxygenation of secondary alcohols
8. Synthese von Nitrilen mit Tetraalkylammoniumcyaniden
9. Stereoselection in the synthesis of threo- and erythro-3-amino-2-hydroxy-4-phenyl-butanoic acid using chiral acetal templates