A mild and efficient route to 2-benzyl tryptamine derivatives via ring-opening of β-carbolines

Tetrahedron

Volumn 64, Issue 42, 2008, Pages 10004-10008

  Hadjaz, Fariza ^a   Yous, Saïd ^a   Lebegue, Nicolas ^a   Berthelot, Pascal ^a   Carato, Pascal ^a  

^a UNIV LILLE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

2 (3 HYDROXYBENZYL)TRYPTAMINE; 2 (3 METHOXYBENZYL)TRYPTAMINE; 2 (3,4 DIMETHOXYBENZYL)TRYPTAMINE; 2 (3,4,5 TRIMETHOXYBENZYL)TRYPTAMINE; 2 (4 METHOXYCARBONYLBENZYL)TRYPTAMINE; 2 (4 METHYLBENZYL)TRYPTAMINE; 2 BENZYLTRYPTAMINE; 5 ETHYL 2 (3 HYDROXYBENZYL) N PROPYL TRYPTAMINE; 5 ETHYL 2 (3 HYDROXYBENZYL)TRYPTAMINE; 5 ETHYL 2 (3 METHOXYBENZYL) N PROPYL TRYPTAMINE; 5 ETHYL 2 (3 METHOXYBENZYL)TRYPTAMINE; 5 ETHYL 2 (3,5 DI TERT BUTYL 4 HYDROXYBENZYL)TRYPTAMINE; BETA CARBOLINE; INDOLE DERIVATIVE; TRYPTAMINE DERIVATIVE; UNCLASSIFIED DRUG;

ALKYLATION; ARTICLE; DRUG SYNTHESIS; HYDROGENATION; PICTET SPENGLER REACTION; PRIORITY JOURNAL; RING OPENING;

EID: 50549091288     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.07.056     Document Type: Article

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