Synthesis of tryptamine derivatives via a direct, one-pot reductive alkylation of indoles

Journal of Organic Chemistry

Volumn 77, Issue 14, 2012, Pages 6351-6357

  Righi, Marika ^a   Topi, Francesca ^a   Bartolucci, Silvia ^a   Bedini, Annalida ^a   Piersanti, Giovanni ^a   Spadoni, Gilberto ^a  

^a UNIVERSITY OF URBINO   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

DIRECT SYNTHESIS; GENERAL METHOD; GRAM-SCALE SYNTHESIS; ONE POT; RECEPTOR ANTAGONISTS; REDUCTIVE ALKYLATION; TRYPTAMINES;

FUNCTIONAL GROUPS; HORMONES;

ALKYLATION;

2,2,2 TRIFLUORO N [2(2 METHYL 1H INDOL 3 YL) ETHYL] ACETAMIDE; 2[2(2 METHYL 1H INDOL 3 YL) ETHYL] ISOINDOLYN 1,3 DIONE; 4 METHYL N [2(2 METHYL 1H INDOL 3 YL) ETHYL] BENZENESULFONAMIDE; ACETAL DERIVATIVE; AMINOETHYL ACETAL DERIVATIVE; BENZYL 2(2 METHYL 1H INDOL 3 YL) ETHYLCARBAMATE; INDOLE DERIVATIVE; LUZINDOLE; MELATONIN; N [2(1 ALLYL 1H INDOL 3 YL) ETHYL] ACETAMIDE; N [2(1 BENZYL 1H INDOL 3 YL) ETHYL] ACETAMIDE; N [2(1 BENZYL 5 METHOXY 1H INDOL 3 YL) ETHYL] ACETAMIDE; N [2(1 METHYL 1H INDOL 3 YL) ETHYL] ACETAMIDE; N [2(1(4 METHOXYBENZYL) 1H INDOL 3 YL) ETHYL] ACETAMIDE; N [2(1,2 DIMETHYL 1H INDOL 3 YL) ETHYL] ACETAMIDE; N [2(2 BENZYL 1H INDOL 3 YL) ETHYL] ACETAMIDE; N [2(2 BUTYL 1H INDOL 3 YL) ETHYL] ACETAMIDE; N [2(2 CYCLOPENTYL 1H INDOL 3 YL) ETHYL] ACETAMIDE; N [2(2 METHYL 1H INDOL 3 YL)ETHYL] ACETAMIDE; N [2(2 METHYL 5(4,4,5,5 TETRAMETHYL 1,3,2 DIOXABOROLAN 2 YL) 1H INDOL 3 YL) ETHYL] ACETAMIDE; N [2(2 PHENYL 1H INDOL 3 YL)ETHYL] ACETAMIDE; N [2(2 TERT BUTYL 1H INDOL 3 YL) ETHYL] ACETAMIDE; N [2(2,5 DIMETHYL 1H INDOL 3 YL) ETHYL] ACETAMIDE; N [2(5 CHLORO 2 METHYL 1H INDOL 3 YL) ETHYL] ACETAMIDE; N [2(5 METHOXY 2 METHYL 1H INDOL 3 YL) ETHYL] ACETAMIDE; N [2(6 METHOXY 2 PHENYL 1H INDOL 3 YL) ETHYL] ACETAMIDE; N,N' [2,2' (1H INDOLE 2,3 DIYL) BIS (ETHANE 2,1 DIYL)] DIACETAMIDE; NITROGEN; TRYPTAMINE DERIVATIVE; UNCLASSIFIED DRUG; UNINDEXED DRUG;

ALKYLATION; ARTICLE; CHEMICAL STRUCTURE; ONE POT SYNTHESIS;

ALKYLATION; INDOLES; MOLECULAR STRUCTURE; STEREOISOMERISM; TRYPTAMINES;

EID: 84864064281     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo3010028     Document Type: Article

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