Michael-induced ring closure to 2-azidocyclopropane-1,1-dicarboxylates and their staudinger reduction to 5-alkoxy-3-(alkoxycarbonyl)pyrrolidin-2-ones

Synlett

Volumn , Issue 3, 2006, Pages 369-374

  Mangelinckx, Sven ^a   De Kimpe, Norbert ^a  

^a GHENT UNIVERSITY   (Belgium)

Author keywords

azido acids; Cyclopropanes; Michael induced ring closure; Ring expansion; Staudinger reduction

Indexed keywords

2 AZIDOALKYLIDENEMALONATE; 2 AZIDOCYCLOPROPANE 1,1 DICARBOXYLATE; 2 BROMOALKYLIDENEMALONATE; 3,3 DIALKYL 2 AZIDOCYCLOPROPANE 1,1 DICARBOXYLATE; 5 ALKOXY 3 (ALKOXYCARBONYL)PYRROLIDIN 2 ONE; BETA AMINOCYCLOPROPANECARBOXYLIC ACID DERIVATIVE; BROMINE DERIVATIVE; CARBOXYLIC ACID DERIVATIVE; CYCLOPROPANE; MALONIC ACID DERIVATIVE; PYRROLIDINE DERIVATIVE; SODIUM AZIDE; UNCLASSIFIED DRUG;

ARTICLE; CONFORMATION; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; REDUCTION; STAUDINGER REACTION; SYNTHESIS;

EID: 33344459023     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2006-926259     Document Type: Article

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