334701-11-0Relevant academic research and scientific papers
Cyclodimerization of indol-2-ylacetylenes. An example of intermolecular enyne-alkyne cycloaddition
Passarella, Daniele,Giardini, Alessandra,Martinelli, Marisa,Silvani, Alessandra
, p. 127 - 129 (2001)
The cyclodimerization of methyl 3-(indol-2-yl)-1-(phenylsulfonyl)acetylene that proceeded through an enzyme-alkyne cycloaddition to give 4-(indol-2-yl)carbazoles was discussed. The behaviour of indolyl-acetylenes bearing an electron-withdrawing group was
A convenient access to 1,3-disubstituted furo[3,4-b]indoles by acid ion-exchange resin-catalyzed furan formation
Basset, Joan,Romero, Manel,Serra, Tha?s,Pujol, M. Dolors
, p. 356 - 362 (2012/01/06)
Efficient synthesis of furo[3,4-b]indoles starting from the corresponding indole is reported. The first route involves derivatization, protection, and deprotection steps, which stretch the syntheses. The second method provides a shorter and more efficient strategy to accessing the furoindole. The innovation starts with alkylation at C-2 of the indole presenting at the C-3 position a ketone-acetal, followed by the cycloaromatization catalyzed by polymeric ion-exchange resins. The second route represents a significant improvement over other methods previously described.
