Electrophilic 2-thienylselenenylation of thiophene. Preparation of oligo (seleno-2, 5-thienylenes)
M Tiecco, L Testaferri, L Bagnoli, F Marini, A Temperini…
Index: Tiecco, Marcello; Testaferri, Lorenzo; Bagnoli, Luana; Marini, Francesca; Temperini, Andrea; Tomassini, Cristina; Santi, Claudio Tetrahedron, 2000 , vol. 56, # 20 p. 3255 - 3260
Full Text: HTML
Citation Number: 15
Abstract
The substitution reactions of thiophene and 2-methylthiophene with the electrophilic selenenylating agent produced from the 2, 2′-dithienyl diselenide by oxidation with iodobenzene diacetate involve only the α-positions and give rise to the formation of oligo (seleno-2, 5-thienylenes). Products deriving from the attack at the α-positions of thiophene and 2-methylthiophene were also observed starting from the 5, 5′-dimethyl-2, 2′- ...
Related Articles:
Mechanism of the lithium iodine exchange in an iodothiophene
[Reich, Hans J.; Whipple, Wesley L. Canadian Journal of Chemistry, 2005 , vol. 83, # 9 p. 1577 - 1587]