175235-80-0Relevant articles and documents
Regioselectivity in the intramolecular heck reaction of a series of cyclic sulfonamides: An experimental and computational study
Geoghegan, Kimberly,Evans, Paul,Rozas, Isabel,Alkorta, Ibon
, p. 13379 - 13387 (2012/11/07)
Regioselectivity in the intramolecular Heck reaction of a series of N-sulfonyl-2,5-dihydro-3-substituted pyrroles was studied. These substrates are unbiased in terms of the formed ring size of the new heterocycle. Results indicate that high levels of regi
Reversible Friedel-Crafts acylations of 3-alkyl-1-(phenylsulfonyl)pyrroles: Application to the synthesis of an ant trail pheromone
Xiao, Dong,Schreier, Jeffrey A.,Cook, James H.,Seybold, Paul G.,Ketcha, Daniel M.
, p. 1523 - 1526 (2007/10/03)
Friedel-Crafts acylations of 3-alkyl-1-(phenylsulfonyl)pyrroles appear to be kinetically favored at the adjacent C-2 position but rearrangement to the C-5 position can occur after prolonged reaction times. This reversible Friedel-Crafts methodology has been employed for the synthesis of the ant trail pheromone, methyl 4-methylpyrrole-2-carboxylate.