Mild and efficient ring opening of monoterpene-fused β-lactamenantiomers. Synthesis of novel b-amino acid derivatives

Arkivoc

Volumn 2003, Issue 14, 2003, Pages 225-232

  Szakonyi, Zsolt ^a   Fülöp, Ferenc ^a  

^a UNIVERSITY OF SZEGED   (Hungary)

Author keywords

b amino acid; b lactam; Enantiomers; Nucleophilic ring opening; Stereoselective synthesis

Indexed keywords

2 AMINOPINANE 3 CARBOXYLIC ACID; 2 TERT BUTYLOXYCARBONYLAMINOPINANE 3 CARBOXYLIC ACID; AMIDE; BETA AMINO ACID; BETA LACTAM; METHYL 2 AMINOPINANE 3 CARBOXYLATE; N TERT BUTYLOXYCARBONYL 2,8,8 TRIMETHYL 3 AZATRICYCLO[5.1.1.0 2,5 ]NONAN 4 ONE; TERPENE; TERT BUTYL [(3 AMINOCARBONYL) 2,6,6 TRIMETHYLBICYCLO[3.1.1]HEPT 2 YL]CARBAMATE; TERT BUTYL [(3 BENZYLAMINOCARBONYL) 2,6,6 TRIMETHYLBICYCLO[3.1.1]HEPT 2 YL]CARBAMATE; TERT BUTYL [(3 METHYLAMINOCARBONYL) 2,6,6 TRIMETHYLBICYCLO[3.1.1]HEPT 2 YL]CARBAMATE; UNCLASSIFIED DRUG;

ARTICLE; DRUG STRUCTURE; DRUG SYNTHESIS; ENANTIOMER; RING OPENING;

EID: 3242739400     PISSN: 14246376     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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