Synthesis of coumarins by ring-closing metathesis using Grubbs' catalyst

Tetrahedron Letters

Volumn 44, Issue 22, 2003, Pages 4199-4201

  Nguyen Van, Tuyen ^a   Debenedetti, Silvia ^a,b   De Kimpe, Norbert ^a  

^a GHENT UNIVERSITY   (Belgium)

^b UNIVERSIDAD NACIONAL DE LA PLATA   (Argentina)

Author keywords

[No Author keywords available]

Indexed keywords

CHLORIDE; COUMARIN DERIVATIVE; PHENOL DERIVATIVE;

ACYLATION; ALLYLATION; ARTICLE; CATALYST; DRUG SYNTHESIS; ISOMERISM; RING CLOSING METATHESIS;

EID: 0038401068     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(03)00902-X     Document Type: Article

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48. It came to our knowledge at the Flohet conference (Gainesville, USA, March 10-12, 2003) that the Grubbs group had independently developed a similar method for the synthesis of coumarins using RCM. In a personal communication, Professor R. Grubbs informed us that their paper was in a status of being in press for publication in Pure and Applied Chemistry (2003). The latter paper focussed on coumarins which were not substituted in the aromatic ring (only substituted at the α,β-unsaturated bond). In that respect, our present results are complimentary to the results of Grubbs group.