A facile synthesis of 4-, 5- and 6-chloromethyl-1H-indole-2-carboxylates: Replacement of a sulfonic acid functionality by chlorine

Tetrahedron

Volumn 60, Issue 40, 2004, Pages 8829-8837

  Pete, Béla ^a   Parlagh, Gyula ^a  

^a BUDAPEST UNIVERSITY OF TECHNOLOGY AND ECONOMICS   (Hungary)

Author keywords

4 (Chloromethyl)indoles; 5 (Chloromethyl)indoles; 6 (Chloromethyl)indoles; Desulfination; Fischer synthesis; Japp Klingemann reaction

Indexed keywords

3 (2 DIMETHYLAMINOETHYL) 5 CHLOROMETHYL 1H INDOLE 2 CARBOXYLIC ACID ETHYL ESTER; 3 (2 METHOXYCARBONYLETHYL) 4 CHLOROMETHYL 1H INDOLE 2 CARBOXYLIC ACID ETHYL ESTER; 3 (2 METHOXYCARBONYLETHYL) 5 CHLOROMETHYL 1H INDOLE 2 CARBOXYLIC ACID ETHYL ESTER; 3 (2 METHOXYCARBONYLETHYL) 6 CHLOROMETHYL 1H INDOLE 2 CARBOXYLIC ACID ETHYL ESTER; 3 (3 METHOXYCARBONYLPROPYL) 4 CHLOROMETHYL 1H INDOLE 2 CARBOXYLIC ACID ETHYL ESTER; 3 (3 METHOXYCARBONYLPROPYL) 5 CHLOROMETHYL 1H INDOLE 2 CARBOXYLIC ACID ETHYL ESTER; 3 (3 METHOXYCARBONYLPROPYL) 6 CHLOROMETHYL 1H INDOLE 2 CARBOXYLIC ACID ETHYL ESTER; 3 (3 PROPYL) 5 CHLOROMETHYL 1H INDOLE 2 CARBOXYLIC ACID ETHYL ESTER; CARBOXYLIC ACID DERIVATIVE; CHLORINE; INDOLE DERIVATIVE; MESYLIC ACID DERIVATIVE; SULFONIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; DRUG SYNTHESIS; PRIORITY JOURNAL; REACTION ANALYSIS;

EID: 4444376212     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2004.07.038     Document Type: Article

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