Divergent synthetic strategy leading to structurally diverse pyrrolidines and piperidines from common γ-aminoalkyl butenolide and aldehyde precursors

Journal of Organic Chemistry

Volumn 71, Issue 23, 2006, Pages 8767-8778

  Aurrecoechea, José M ^a   Suero, Rúben ^a   De Torres, Esther ^a  

^a UNIVERSITY OF THE BASQUE COUNTRY UPV EHU   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

ADDITION REACTIONS; ALDEHYDES; CONDENSATION; HYDROGENATION; ISOMERIZATION; REDUCTION; SAMARIUM COMPOUNDS; SYNTHESIS (CHEMICAL);

AMINOALKYLBENZOTRIAZOLES; ISOMERIC PIPERIDINE ANALOGUES; LACTONE MOIETY; PRECURSORS;

NITROGEN COMPOUNDS;

2 PIPERIDEINE DERIVATIVE; ALDEHYDE DERIVATIVE; ALKENE DERIVATIVE; ALKYL GROUP; BENZOTRIAZOLE DERIVATIVE; BUTENOLIDE; FURAN DERIVATIVE; IMINE; LACTONE; PIPERIDINE DERIVATIVE; PYRIDINE DERIVATIVE; PYRROLIDINE DERIVATIVE; SILANE DERIVATIVE; UNCLASSIFIED DRUG;

ADDITION REACTION; ARTICLE; CHEMICAL REACTION; DIASTEREOISOMER; HYDROGENATION; ISOMERISM; POLYMERIZATION; PRECURSOR; REACTION ANALYSIS; REDUCTION; STRUCTURE ANALYSIS; SYNTHESIS;

4-BUTYROLACTONE; ALDEHYDES; CYCLIZATION; FREE RADICALS; MOLECULAR STRUCTURE; PIPERIDINES; PYRROLIDINES; STEREOISOMERISM;

EID: 33750859984     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0614487     Document Type: Article

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