A highly regioselective ring-opening metathesis-cross metathesis process modulated by the electronic effects of the cross metathesis partner: An entry to quaternary prolines

Journal of Organic Chemistry

Volumn 74, Issue 4, 2009, Pages 1736-1739

  Carreras, Javier ^a   Avenoza, Alberto ^a   Busto, Jesús H ^a   Peregrina, Jesús M ^a  

^a UNIVERSITY OF LA RIOJA   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

ACRYLIC ACID METHYL ESTER; ALKENE; AMINO ACID; BENZENE DERIVATIVE; PHENYLVINYLTHIOETHER; PROLINE; SULFIDE; UNCLASSIFIED DRUG; VINYL DERIVATIVE;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CATALYST; CHEMICAL REACTION; CHEMICAL STRUCTURE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; PROTON NUCLEAR MAGNETIC RESONANCE; RING OPENING; RING OPENING CROSS METATHESIS; SYNTHESIS;

ALKENES; CARBOXYLIC ACIDS; ELECTRONS; PROLINE; STEREOISOMERISM; SUBSTRATE SPECIFICITY;

EID: 64349121797     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo802399k     Document Type: Article

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