An entry to the azocino[4,3- b ]indole framework through a dehydrogenative activation of 1,2,3,4-tetrahydrocarbazoles mediated by DDQ: Formal synthesis of (±)-uleine

Journal of Organic Chemistry

Volumn 76, Issue 1, 2011, Pages 335-338

  Patir, Süleyman ^a   Ertürk, Erkan ^b  

^a HACETTEPE UNIVERSITY   (Turkey)

^b MATERIALS INSTITUTE   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

AMIDE FUNCTIONALITIES; CASCADE REACTIONS; CYCLIZATION REACTIONS; FORMAL SYNTHESIS; HIGH YIELD; IMINIUM CATION; SELECTIVE ADDITION; TOTAL SYNTHESIS;

AMIDES; POSITIVE IONS; SYNTHESIS (CHEMICAL);

CYCLIZATION;

1,2,3,4 TETRAHYDROCARBAZOLE DERIVATIVE; 2,3 DICHLORO 5,6 DICYANOBENZOQUINONE; ALKALOID DERIVATIVE; AMIDE; AZOCINO[4,3 B]INDOLE; BENZOQUINONE DERIVATIVE; IMINE; INDOLE DERIVATIVE; NUCLEOPHILE; ULEINE; UNCLASSIFIED DRUG;

ARTICLE; CYCLIZATION; DEHYDROGENATION; REACTION ANALYSIS; SYNTHESIS;

ALKALOIDS; AZOCINES; BENZOQUINONES; BRIDGED COMPOUNDS; CARBAZOLES; CYCLIZATION; INDOLES; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR STRUCTURE; STEREOISOMERISM;

EID: 78650886244     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo1021663     Document Type: Article

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