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Volumn 17, Issue 1, 2013, Pages 55-61

An efficient and facile synthesis of 3-amino-5-chromenyl-butenolides from 3-formyl chromone, dialkyl acetylenedicarboxylate, and primary amines

Author keywords

3 Amino 5 chromenyl butenolides; Chromones; Enaminones; MCR; Multicomponant reactions

Indexed keywords

AMINE; BUTENOLIDE; CHROMONE DERIVATIVE; DICARBOXYLIC ACID; ETHYL 2 (6 CHLORO 4 OXO 4H CHROMEN 3 YL) 2,5 DIHYDRO 4 (ISOBUTYLAMINO) 5 OXOFURAN 3 CARBOXYLATE; ETHYL 4 (1 PHENYLETHYLAMINO) 2 (6 CHLORO 4 OXO 4H CHROMEN 3 YL) 2,5 DIHYDRO 5 OXOFURAN 3 CARBOXYLATE; ETHYL 4 (ALLYLAMINO) 2 (6 CHLORO 4 OXO 4H CHROMEN 3 YL) 2,5 DIHYDRO 5 OXOFURAN 3 CARBOXYLATE; ETHYL 4 (ALLYLAMINO) 2,5 DIHYDRO 5 OXO 2 (4 OXO 4H CHROMEN 3 YL)FURAN 3 CARBOXYLATE; ETHYL 4 (BENZYLAMINO) 2 (6 CHLORO 4 OXO 4H CHROMEN 3 YL) 2,5 DIHYDRO 5 OXOFURAN 3 CARBOXYLATE; ETHYL 4 (BENZYLAMINO) 2,5 DIHYDRO 5 OXO 2 (4 OXO 4H CHROMEN 3 YL)FURAN 3 CARBOXYLATE; METHYL 2 (6 CHLORO 4 OXO 4H CHROMEN 3 YL) 2,5 DIHYDRO 4 (ISOBUTYLAMINO) 5 OXOFURAN 3 CARBOXYLATE; METHYL 4 (1 BENZYLAMINO) 2 (6 CHLORO 4 OXO 4H CHROMEN 3 YL) 2,5 DIHYDRO 5 OXOFURAN 3 CARBOXYLATE; METHYL 4 (1 PHENYLETHYLAMINO) 2 (6 CHLORO 4 OXO 4H CHROMEN 3 YL) 2,5 DIHYDRO 5 OXOFURAN 3 CARBOXYLATE; METHYL 4 (ALLYLAMINO) 2 (6 CHLORO 4 OXO 4H CHROMEN 3 YL) 2,5 DIHYDRO 5 OXOFURAN 3 CARBOXYLATE; METHYL 4 (ALLYLAMINO) 2,5 DIHYDRO 5 OXO 2 (4 OXO 4H CHROMEN 3 YL)FURAN 3 CARBOXYLATE; NUCLEOPHILE; UNCLASSIFIED DRUG;

EID: 84873406907     PISSN: 13811991     EISSN: 1573501X     Source Type: Journal    
DOI: 10.1007/s11030-013-9423-4     Document Type: Article
Times cited : (10)

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