An alternative approach to the synthesis of functionalized pyrido[2,3-b]indoles

Tetrahedron

Volumn 57, Issue 22, 2001, Pages 4787-4792

  Beccalli, Egle M ^a   Clerici, Francesca ^a   Marchesini, Alessandro ^a  

^a UNIVERSITY OF MILAN   (Italy)

Author keywords

carbolines; Enamines; Oxindoles; Thermal cyclization

Indexed keywords

3 (1 ETHOXYCARBONYL 3 MORPHOLIN 4 YL 2 PHENYLALLYLIDENE) 2 OXO 2,3 DIHYDRO INDOLE 1 CARBOXYLIC ACID ETHYL ESTER; 3 (1 ETHOXYCARBONYL 3 MORPHOLIN 4 YL 3 PHENYLALLYLIDENE) 2 OXO 2,3 DIHYDRO INDOLE 1 CARBOXYLIC ACID ETHYL ESTER; 3 (3 AMINO 2 METHOXYCARBONYL BUT 2 ENYLIDENE) 2 OXO 2,3 DIHYDRO INDOLE 1 CARBOXYLIC ACID ETHYL STER; 3 (3 MORPHOLIN 4 YL 2 PHENYL 1 TRIFLUOROMETHYLALLYLIDENE) 2 OXO 2,3 DIHYDRO INDOLE 1 CARBOXYLIC ACID ETHYL ESTER; 3 (3 MORPHOLIN 4 YL 2 PHENYLALLYLIDENE) 2 OXO 2,3 DIHYDRO INDOLE 1 CARBOXYLIC ACID ETHYL ESTER; 3 (3 MORPHOLIN 4 YL 3 PHENYLALLYLIDENE) 2 OXO 2,3 DIHYDRO INDOLE 1 CARBOXYLIC ACID ETHYL ESTER; 3 INDOL 2(3H) ONE DERIVATIVE; ACETIC ACID; ALPHA CARBOLINE DERIVATIVE; AMMONIUM ACETATE; CARBOLINE DERIVATIVE; ENAMINE; ESTER DERIVATIVE; INDOLE DERIVATIVE; KETONE DERIVATIVE; PYRIDO[2,3 B]INDOLE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; CYCLIZATION; PRIORITY JOURNAL; SYNTHESIS;

EID: 0035962769     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(01)00404-5     Document Type: Article

References (20)