84289-38-3Relevant academic research and scientific papers
Access to 2-Arylindoles via Decarboxylative C?C Coupling in Aqueous Medium and to Heteroaryl Carboxylates under Base-Free Conditions using Diaryliodonium Salts
Arun, Velladurai,Pilania, Meenakshi,Kumar, Dalip
, p. 3345 - 3349 (2016)
Easily accessible heteroaromatic carboxylic acids and diaryliodonium salts were successfully employed to construct valuable 2-arylindoles and heteroaryl carboxylates in a regioselective fashion. C2-arylated indoles were produced using a Pd-catalyzed decarboxylative strategy in water without any base, oxidant, or ligand. Heteroaryl carboxylates were prepared under metal and base-free conditions. This protocol was successfully utilized to synthesize Paullone, a cyclin-dependent kinase (CDK) inhibitor.
Auxin compositions of phenyl thioesters of indole-3-alkanoic acids and their use as auxin growth regulators
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, (2008/06/13)
Aryl esters and thioesters of indole-3-alkanoic acids, such as indole-3-acetaic acid and indole-3-butyric acid, are prepared by chemical reaction of the acid with a phenol, substituted phenol, or thiophenol in a tertiary amine solvent. A phosphorus or sul
