Facile synthesis of coumarin- and quinolone-annulated benzazoninone derivatives by an intramolecular heck reaction strategy via 9- exo -trig cyclization

Synthesis

Volumn , Issue 10, 2011, Pages 1569-1574

  Majumdar, K C ^a   Ghosh, Tapas ^a   Samanta, Srikanta ^a  

^a UNIVERSITY OF KALYANI   (India)

Author keywords

aza Claisen rearrangement; benzazoninones; coumarin; Heck reaction; quinolone

Indexed keywords

AZA-CLAISEN REARRANGEMENT; BENZAZONINONES; COUMARIN; HECK REACTIONS; QUINOLONES;

SYNTHESIS (CHEMICAL);

CYCLIZATION;

4,7 DIMETHYL 14 METHYLENE 7,9,14,15 TETRAHYDRO 3H QUINO[6,5 D] [3] BENZAZONINE 3,8 (4H) DIONE; 5 ALLYL 6 (METHYLAMINO)COUMARIN; 5 METHYL 12 METHYLENE 12,13 DIHYDRO 5H DIBENZO[B,F]AZONIN 6 (7H) ONE; 7 ETHYL 4 METHYL 14 METHYLENE 7,9,14,15 TETRAHYDRO 3H QUINO [6,5 D] [3] BENZAZONINE 3,8 (4H) DIONE; 7 METHYL 14 METHYLENE 14,15 DIHYDROBENZO[F]CHROMENO [6,5 B]AZONINE 3,8 (7H,9H) DIONE; BENZAZOCINE DERIVATIVE; COUMARIN DERIVATIVE; N (2 ALLYLPHENYL) 2 (2 IODOPHENYL) N METHYLACETAMIDE; N (2 ALLYLPHENYL) N ETHYL 2 (2 IODOPHENYL)ACETAMIDE; N (5 ALLYL 1 METHYL 2 OXO 1,2 DIHYDROQUINOLIN 6 YL) 2 (2 IODOPHENYL) M METHYLACETAMIDE; N (5 ALLYL 1 METHYL 2 OXO 1,2 DIHYDROQUINOLIN 6 YL) N ETHYL 2 (2 IODOPHENYL)ACETAMIDE; N (5 ALLYL 2 OXO 2H CHROMEN 6 YL) 2 (2 IODOPHENYL) N METHYLACETAMIDE; N (5 ALLYL 2 OXO 2H CHROMEN 6 YL) N ETHYL 2 (2 IODOPHENYL)ACETAMIDE; QUINOLONE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CATALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; CLAISEN REARRANGEMENT; CYCLIZATION; DRUG SYNTHESIS; ENTROPY; HECK REACTION; MELTING POINT;

EID: 79955866849     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0030-1260005     Document Type: Article

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