Diastereo- and enantioselective synthesis of orthogonally protected 2,4-diaminocyclopentanecarboxylates: A flip from β-amino- to β,γ-diaminocarboxylates

Journal of Organic Chemistry

Volumn 72, Issue 23, 2007, Pages 8786-8790

  Kiss, Loránd ^a   Forró, Enikó ^a   Sillanpää, Reijo ^c   Fülöp, Ferenc ^a,b  

^a UNIVERSITY OF SZEGED   (Hungary)

^b UNIVERSITY OF SZEGED   (Hungary)

^c UNIVERSITY OF JYVÄSKYLÄ   (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

DIASTEREOSELECTIVITY; SODIUM AZIDE;

AMINO ACIDS; ENANTIOMERS; ENANTIOSELECTIVITY; ESTERS; STEREOSELECTIVITY;

CARBOXYLIC ACIDS;

2,4 DIAMINOCYCLOPENTANECARBOXYLIC ACID DERIVATIVE; BETA AMINO DIAMINOCARBOXYLIC ACID DERIVATIVE; BETA LACTAM; BETA,GAMMA DIAMINOCARBOXYLIC ACID DERIVATIVE; CARBOCYCLIC NUCLEOSIDE; CARBOXYLIC ACID DERIVATIVE; CYCLOPENTANE DERIVATIVE; ETHYLENE OXIDE; SODIUM AZIDE; UNCLASSIFIED DRUG;

ARTICLE; CONFORMATIONAL TRANSITION; DIASTEREOISOMER; ENANTIOSELECTIVITY; EPOXIDATION; RING OPENING; STEREOCHEMISTRY; STRUCTURE ANALYSIS; SYNTHESIS;

BETA-LACTAMS; CARBOXYLIC ACIDS; CYCLOPENTANES; ESTERS; ETHYLENE OXIDE; MOLECULAR CONFORMATION; SODIUM AZIDE; STEREOISOMERISM;

EID: 35948988421     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo701332v     Document Type: Article

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