1071469-55-0Relevant articles and documents
Synthesis and antidepressant-like activity of selenophenes obtained via iron(iii)-PhSeSePh-mediated cyclization of Z-selenoenynes
Gai, Bibiana M.,Stein, Andre L.,Roehrs, Juliano A.,Bilheri, Filipe N.,Nogueira, Cristina W.,Zeni, Gilson
supporting information; experimental part, p. 798 - 807 (2012/02/05)
We present here the synthesis and antidepressant-like action of a series of 2,5-disubstituted-3-(organoseleno)-selenophenes prepared by a novel synthetic route, the FeCl3-diorganyl dichalcogenide-mediated intramolecular cyclization of (Z)-chalc
Copper iodide-catalyzed cyclization of (Z)-chalcogenoenynes
Stein, Andre L.,Alves, Diego,Da Rocha, Juliana T.,Nogueira, Cristina W.,Zeni, Gilson
scheme or table, p. 4983 - 4986 (2009/05/07)
(Chemical Equation Presented) We present here our results of the efficient copper-catalyzed cyclizations of chalcogenoenynes and establish a route to obtain 3-substituted chalcogenophenes in good to excellent yields. In addition, the obtained chalcogenophenes were readily transformed to more complex products using the palladium-catalyzed cross-coupling reactions with boronic acids to give Suzuki-type products in good yields.
