A mild and efficient method for the synthesis of a new class of furo[3,2-c]chromenes in aqueous media

Molecular Diversity

Volumn 15, Issue 2, 2011, Pages 445-450

  Khalilzadeh, Mohammad A ^a   Hossaini, Zinatossadat ^a   Charati, Faramarz Rostami ^b   Hallajian, Sara ^a   Rajabi, Mehdi ^c  

^a Islamic Azad University   (Iran)

^b Gonbad Higher Education Center   (Iran)

^c UNIVERSITY OF MILAN   (Italy)

Author keywords

4 hydroxycoumarine; Chromenes; Dibenzoylacetylene; Furo 3,2 c chromene 1 ium cation; Naphthofurans; Oxonium cation

Indexed keywords

2 (DIETHYLAMINO) 3 [2 OXO 2 PHENYLETHYLIDENE] 2 PHENYL 4H FURO[3,2 C]CHROMEN 4(2H) ONE; 2 (DIMETHYLAMINO) 3 [2 OXO 2 PHENYLETHYLIDENE] 2 PHENYL 4H FURO[3,2 C]CHROMEN 4(2H) ONE; 2 (MORPHOLINO) 3 [2 OXO 2 PHENYLETHYLIDENE] 2 PHENYL 4H FURO[3,2 C]CHROMEN 4(2H) ONE; 2 (PIPERIDINYL) 3 [2 OXO 2 PHENYLETHYLIDENE] 2 PHENYL 4H FURO[3,2 C]CHROMEN 4(2H) ONE; 2 (PYRROLIDINYL) 3 [2 OXO 2 PHENYLETHYLIDENE] 2 PHENYL 4H FURO[3,2 C]CHROMEN 4(2H) ONE; 2 ETHOXY 3 [2 OXO 2 PHENYLETHYLIDENE] 2 PHENYL 4H FURO[3,2 C]CHROMEN 4(2H) ONE; 2 HYDROXY 3 [2 OXO 2 PHENYLETHYLIDENE] 2 PHENYL 2,3 DIHYDRO 4H FURO[3, 2 C]CHROMENE 4(2H) ONE; 2 ISOPROPOXY 3 [2 OXO 2 PHENYLETHYLIDENE] 2 PHENYL 4H FURO[3,2 C]CHROMEN 4(2H) ONE; 2 METHOXY 3 [2 OXO 2 PHENYLETHYLIDENE] 2 PHENYL 4H FURO[3,2 C]CHROMEN 4(2H) ONE; 2 PROPOXY 3 [2 OXO 2 PHENYLETHYLIDENE] 2 PHENYL 4H FURO[3,2 C]CHROMEN 4(2H) ONE; 2 PROPYNYLOXY 3 [2 OXO 2 PHENYLETHYLIDENE] 2 PHENYL 4H FURO[3,2 C]CHROMEN 4(2H) ONE; 4 OXO 3 [2 OXO 2 PHENYLETHYLIDENE] 2 PHENYL 3H,4H FURO[3,2 C]CHROMEN 1 IUM; CHROMENE DERIVATIVE; DIMETHYL [4 OXO 3 [2 OXO 2 PHENYLETHYLIDENE] 2 PHENYL 2,3 DIHYDRO 4H FURO[3,2 C]CHROMEN 2 YL]PHOSPHONATE; FURO[3,2 C]CHROMENE DERIVATIVE; UNCLASSIFIED DRUG; ALCOHOL DERIVATIVE; AMINE; BENZOPYRAN DERIVATIVE;

ADDITION REACTION; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; DRUG STRUCTURE; DRUG SYNTHESIS; INFRARED RADIATION; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; CHEMISTRY; METHODOLOGY; SYNTHESIS;

ALCOHOLS; AMINES; BENZOPYRANS; CHEMISTRY;

EID: 80051575233     PISSN: 13811991     EISSN: 1573501X     Source Type: Journal    
DOI: 10.1007/s11030-010-9264-3     Document Type: Article

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