Synthesis of new 2-vinylation products of indole via a Michael-type addition reaction with dimethyl acetylenedicarboxylate and their diels-alder reactivity as precursors of new carbazoles

Journal of Organic Chemistry

Volumn 71, Issue 20, 2006, Pages 7793-7799

  Çavdar, Hüseyin ^a   Saraçoǧlu, Nurullah ^a  

^a ATATÜRK UNIVERSITY   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

ADDITION REACTIONS; ANNEALING; AROMATIC COMPOUNDS; SYNTHESIS (CHEMICAL);

DIELS-ALDER REACTIONS; DIMETHYL ACETYLENEDICARBOXYLATE; TETRACYANOETHYLENE;

NITROGEN COMPOUNDS;

1,2 DICYANO 4,5 DICHLOROQUINONE; 1,4 BENZOQUINONE; 2 VINYLINDOLE DERIVATIVE; 4,7 DIHYDROINDOLE; ACETYLENEDICARBOXYLIC ACID DIMETHYL ESTER; CARBAZOLE DERIVATIVE; INDOLE DERIVATIVE; N PHENYLTRIAZOLINEDIONE; NAPHTHOQUINONE; QUINONE DERIVATIVE; TETRACYANOETHYLENE; TRIAZOLINE DERIVATIVE; UNCLASSIFIED DRUG; VINYL DERIVATIVE;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; DIELS ALDER REACTION; MICHAEL ADDITION; ORGANIC CHEMISTRY; STRUCTURE ANALYSIS; SYNTHESIS;

CARBAZOLES; CARBOXYLIC ACIDS; INDOLES; MOLECULAR STRUCTURE; VINYL COMPOUNDS;

EID: 33749131944     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo061336f     Document Type: Article

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