Regio and diastereoselective synthesis of functionalized 2,3-dihydrofuro[3,2-c]coumarins via a one-pot three-component reaction

Tetrahedron

Volumn 66, Issue 49, 2010, Pages 9493-9496

  Altieri, Elisa ^a   Cordaro, Massimiliano ^a   Grassi, Giovanni ^a   Risitano, Francesco ^a   Scala, Angela ^a  

^a UNIVERSITY OF MESSINA   (Italy)

Author keywords

4 Hydroxycoumarin; Cyclization; Diastereoselectivity; Multicomponent reaction

Indexed keywords

2,3 DIHYDROFURO[3,2 C] COUMARIN; 4 HYDROXYCOUMARIN; ALDEHYDE; COUMARIN DERIVATIVE; KETONE; PROPANOL; PYRIDINE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CATALYST; CHEMICAL STRUCTURE; CYCLIZATION; ONE POT SYNTHESIS; POLYMERIZATION; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY;

EID: 78149465820     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2010.10.023     Document Type: Article

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28. 3).
29. Under these conditions, no reaction occurred with aliphatic aldehydes 2j, k or with aliphatic α-halogen ketones 4 and 5.
30. Our one-pot procedure is more convenient with respect to Ref.12 in terms of yield and reaction time.
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