N-alkenyl indoles as useful intermediates for alkaloid synthesis

Journal of Organic Chemistry

Volumn 76, Issue 22, 2011, Pages 9488-9496

  Li, Hao ^a   Boonnak, Nawong ^a   Padwa, Albert ^a  

^a EMORY UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALKENYL; COPPER IODIDE; COUPLING PROCEDURE; CROSS COUPLING REACTIONS; CYCLIZATION REACTIONS; CYCLOPENTANOL; ENAMINES; ETHYLENE DIAMINE; INDOLE DERIVATIVES; INDOLE RINGS; PROTONATION REACTIONS; QUATERNARY STEREOCENTERS; RADICAL CYCLIZATIONS; SELECTIVE FUNCTIONALIZATION;

BROMINE COMPOUNDS; ETHERS; METABOLITES; NITROGEN COMPOUNDS; REACTION INTERMEDIATES; SYNTHESIS (CHEMICAL);

CYCLIZATION;

12 AMINO 2,3,3A,4,11,12,12A,12B OCTAHYDRO 10 HYDROXYISOQUINO[2,1,8 LMA]CARBAZOL 5(1H) ONE; 2 [2 (1H INDOL 1 YL)ALLYL]CYCLOPENTANONE; 3 METHYL 1 (PROP 1 EN 2 YL) 1H INDOLE; ALKALOID; COPPER IODIDE; DIMETHYL 1,1' (4 METHYLPENT 1 ENE 2,4 DIYL)BIS(1H INDOLE 3 CARBOXYLATE); ETHYLENEDIAMINE; INDOLE DERIVATIVE; IODIDE; METHYL 1 (1 BROMOBUT 2 EN 2 YL) 1H INDOLE 3 CARBOXYLATE; METHYL 1 (2,6A DIMETHYLHEXAHYDRO 2H CYCLOPENTA[B]FURAN 2 YL) 1H INDOLE 3 CARBOXYLATE; METHYL 1 (BUT 1 EN 2 YL) 1H INDOLE 3 CARBOXYLATE; METHYL 1 [3 (2 HYDROXY 2 METHYLCYCLOPENTYL)PROP 1 EN 2 YL] 1H INDOLE 3 CARBOXYLATE; METHYL 1 [3 (2 HYDROXY 2 PHENYLCYCLOPENTYL)PROP 1 EN 2 YL] 1H INDOLE 3 CARBOXYLATE; METHYL 1 [3 (2 OXOCYCLOHEXYL)PROP 1 EN 2 YL] 1H INDOLE 3 CARBOXYLATE; METHYL 1 [3 (2 OXOCYCLOPENTYL)PROP 1 EN 2 YL] 1H INDOLE 3 CARBOXYLATE; METHYL 1 [3 [2 [[(METHYLTHIO)CARBONOTHIOYL]OXY]CYCLOHEXYL]PROP 1 EN 2 YL] 1H INDOLE 3 CARBOXYLATE; METHYL 1 [3 [2 [[(METHYLTHIO)CARBONOTHIOYL]OXY]CYCLOPENTYL]PROP 1 EN 2 YL] 1H INDOLE 3 CARBOXYLATE; METHYL 5 METHYL 11B PHENYL 2,3,3A,11B TETRAHYDRO 1H CYCLOPENTA[3,4]PYRIDO [1,2 A]INDOLE 11 CARBOXYLATE; N ALKENYL INDOLE DERIVATIVE; UNCLASSIFIED DRUG; VINBURNINE;

ARTICLE; CROSS COUPLING REACTION; CYCLIZATION;

ALKALOIDS; ALKENES; CATALYSIS; COPPER; CROSS-LINKING REAGENTS; CYCLIZATION; HETEROCYCLIC COMPOUNDS WITH 4 OR MORE RINGS; INDOLES; MOLECULAR STRUCTURE; STEREOISOMERISM; VINCA ALKALOIDS;

EID: 81055144514     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo201955c     Document Type: Article

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