One-pot synthesis of N-protected β-chiral amino alcohols

Synthetic Communications

Volumn 33, Issue 11, 2003, Pages 1815-1820

  Somlai, Csaba ^a   Péter, Antal ^a   Forgó, Péter ^a   Penke, Botond ^a  

^a UNIVERSITY OF SZEGED   (Hungary)

Author keywords

Amino alcohols; Enantiopurity; Reduction

Indexed keywords

AMINOALCOHOL; ESTER; N FLUORENYLMETHYLOXYCARBONYLALANINE; N TERT BUTYLOXYCARBONYL S BENZYLCYSTEINE; O TERT BUTYLTYROSINE; S TRITYLCYSTEINE; SODIUM BOROHYDRIDE; UNCLASSIFIED DRUG;

ARTICLE; CHIRALITY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; PROTON NUCLEAR MAGNETIC RESONANCE; PURIFICATION; REDUCTION; SYNTHESIS;

EID: 0038583566     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1081/SCC-120020188     Document Type: Article

References (4)

1. 2) and its application to gas chromatographic analysis of fatty acids. Chem. Pharm. Bull. 1981, 29 (5), 1475-1478.
2. [1] A practical method for the preparation of optically active N-protected-amino aldehydes and peptide aldehydes. 1982, 30, 1921-1924.
3. Hamada, Y.; Shibata, M.; Sugiura, T.; Kato, S.; Shiori, T. New methods and reagents in organic synthesis. 67. A general synthesis of derivatives of optically pure 2-(1-aminoalkyl)thiazole-4-carboxylic acids. J. Org. Chem. 1987, 52, 1252-1255.
4. McKay, A.F.; Wright, George F.J. Preparation and properties of N-Methyl-N-nitroso-N′-nitroguanidine. J. Am. Chem. Soc. 1947, 69, 3028-3030.