1033757-55-9Relevant academic research and scientific papers
SeCl2-Mediated Approach Toward Indole-Containing Polysubstituted Selenophenes
Martins, Guilherme M.,Back, Davi F.,Kaufman, Teodoro S.,Silveira, Claudio C.
, p. 3252 - 3264 (2018/03/25)
A novel and efficient SeCl2-mediated chalcogenative cyclization strategy toward 3-selenophen-3-yl-1H-indoles from readily available and conveniently substituted propargyl indoles is described. It entails an unprecedented selenirenium-induced 1,
Bronsted acid catalyzed alkylation of indoles with tertiary propargylic alcohols: Scope and limitations
Sanz, Roberto,Miguel, Delia,Martinez, Alberto,Gohain, Mukut,Garcia-Garcia, Patricia,Fernandez-Rodriguez, Manuel A.,Alvarez, Estela,Rodriguez, Felix
supporting information; experimental part, p. 7027 - 7039 (2011/02/28)
Direct alkylation of indoles with a wide variety of tertiary propargylic alcohols under Bronsted acid catalysis conditions has been studied. A general and environmentally friendly method for the synthesis of 3-propargylated indoles with quaternary carbon
Br?nsted acid catalyzed C3-selective propargylation and benzylation of indoles with tertiary alcohols
Sanz, Roberto,Miguel, Delia,álvarez-Gutiérrez, Julia M.,Rodríguez, Félix
experimental part, p. 975 - 978 (2009/04/04)
A Br?nsted acid catalyzed C3-selective tert-alkylation of indoles using tertiary propargylic and benzylic alcohols has been developed. New C3-propargylated indole derivatives with a quaternary carbon at the propargylic position have been efficiently synth
