1670-83-3Relevant articles and documents
Palladium-Catalyzed Carbonylation of Haloindoles: No Need for Protecting Groups
Kumar, Kamal,Zapf, Alexander,Michalik, Dirk,Tillack, Annegret,Heinrich, Timo,Boettcher, Henning,Arlt, Michael,Beller, Matthias
, p. 7 - 10 (2004)
(Equation presented) For the first time, palladium-catalyzed carbonylations of unprotected bromoindoles have been performed successfully with different N- and 0-nucleophiles. Various indole carboxylic acid derivatives are accessible in excellent yield. For example, aminocarbonylation of 4-, 5-, 6-, or 7-bromoindole with arylethylpiperazines provides a direct one-step synthesis for CNS active amphetamine derivatives.
NEW SYNTHESIS OF INDOLE-7-CARBOXYLIC ACID
Dulenko, V. I.,Nikolyukin, Yu. A.
, p. 36 - 37 (1986)
A new preparative method for synthesis of indole-7-carboxylic acid has been developed, consisting in reductive cyclization of β-(dimethylamino)-3-carbomethoxy-2-nitrostyrene by the action of iron in acetic acid.