1(2,6-dichlorophenyl)ethylamine: a new and efficient chiral auxiliary for the Staudinger β-lactam synthesis

Tetrahedron Letters

Volumn 36, Issue 48, 1995, Pages 8821-8824

  Hashimoto, Yukihiko ^a   Kai, Akiyoshi ^a   Saigo, Kazuhiko ^a  

^a UNIVERSITY OF TOKYO   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

BETA LACTAM DERIVATIVE;

ARTICLE; CHIRALITY; DRUG SYNTHESIS; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; REACTION ANALYSIS;

EID: 0028789812     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(95)01883-J     Document Type: Article

References (21)

1. Optical Resolution of 1-(3-Methoxyphenyl)ethylamine with Enantiomerically Pure Mandelic Acid, and the Crystal Structure of Less-Soluble Diastereomeric Salt.
2. Optical resolution of erythro-2-amino-1,2-diphenylethanol by reciprocal crystallization of the diastereomeric salts with (-)-mandelic acid on alternate seeding.
3. Optical resolution of 2-amino-1,2-diphenylethanol by preferential crystallization and its utilization in fractional crystallization and enantioselective reduction of prochiral ketones.
4. Stereoselective Addition Reaction of Organolithium Reagents to Chiral Imines Derived from erythro-2-Amino-1,2-diphenylethanol.
5. Effective method for the asymmetric synthesis of bis-β-lactams by the cycloaddition of azidoketen to benzylideneamines bearing a chiral β-lactam backbone
6. A Novel Stereocontrolled Synthesis of 3-(1′-Hydroxyethyl)-2-Azetidinone