2-(N-Methylanilino)-3-formylchromone - A versatile synthon for incorporation of chromone moiety in a variety of heterocyclic systems and macrocycles through reactions with bifunctional nucleophiles

Tetrahedron

Volumn 58, Issue 39, 2002, Pages 7883-7890

  Singh, Gurmit ^a   Singh, Lakhwinder ^a   Ishar, M P S ^a  

^a GURU NANAK DEV UNIVERSITY   (India)

Author keywords

Addition elimination; Chromano azepines; Chromano oxazepines; Chromano quinolines; Chromano thiazapine; Chromanopyrazoles; Chromanopyrole; Chromones; Condensation; Macrocycles

Indexed keywords

1,1' BIS(4 OXO 3 FORMYL 4H[1]BENZOPYRAN 2 YL) 4,4' BIPIPERIDINE; 2 (N METHYLANILINO) 3 FORMYLCHROMONE; 2 CHLORO 8 AMINOQUINOLINO[2,2 B]CHROMAN 12 ONE; 2 CHLORO[1]BENZOPYRANO[2,3 B][1,5]BENZOTHIAZEPIN 13 ONE; 2 CHLORO[1]BENZOPYRANO[2,3 B][1,5]BENZOXAZEPIN 13 ONE; 2 METHOXYCARBONYL[1]BENZOPYRANO[2,3 B]PYRROL 4 ONE; 2 METHOXYCARBONYLMETHYLAMINO 3 FORMYLCHROMONE; 6 CHLORO 1 PHENYL[1]BENZOPYRANO[2,3 C]PYRAZOL 4 ONE; 6H [1]BENZOPYRANO[2,3 B][1,5]BENZODIAZEPIN 13 ONE; 8 AMINOQUINOLINO[2,3 B]CHROMAN 12 ONE; [1]BENZOPYRANO[2,3 B][1,5]BENZOXAZEPIN 13 ONE; CHROMONE DERIVATIVE; FUNCTIONAL GROUP; HETEROCYCLIC COMPOUND; LIGAND; MACROCYCLIC COMPOUND; N,N' BIS(4 OXO 3 FORMYL 4H[1]BENZOPYRAN 2 YL) 3 XYLENEDIAMINE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL MODIFICATION; DRUG SYNTHESIS; PRIORITY JOURNAL; REACTION ANALYSIS;

EID: 0037163298     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(02)00908-0     Document Type: Article

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