Tetrahedron Letters p. 1523 - 1526 (1996)
Update date:2022-08-05
Topics:
Xiao, Dong
Schreier, Jeffrey A.
Cook, James H.
Seybold, Paul G.
Ketcha, Daniel M.
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.
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Doi:10.1016/0040-4039(95)02388-7
(1996)Doi:10.1246/bcsj.69.1139
(1996)Doi:10.1016/0022-328X(95)05787-P
(1996)Doi:10.1016/0040-4039(96)00323-1
(1996)Doi:10.1006/bioo.1996.0004
(1996)Doi:10.1039/CC9960000127
(1996)
