Lewis acid-mediated domino reaction of 3-bromomethylthiophenes with arenes/heteroarenes
Lewis acid-mediated domino reaction of 3-bromomethylthiophenes with various types of arenes and heteroarenes is reported.
Dhayalan, Vasudevan,Mohanakrishnan, Arasambattu K.
experimental part
p. 2149 - 2160
(2012/06/16)
Thienopyrroles: Synthesis, Diels-ALder Reaction, and Synthetic Utility
5H-Thienopyrrole 1a and the N-substituted derivatives 1b-h and 11-13 were synthesized by the novel retro-malonate addition reaction.Thienopyrroles readily underwent the Diels-Alder reaction with reactive dienophiles, such as N-phenylmaleimid
Sha, Chin-Kang,Tsou, Chiu-Peng
p. 2446 - 2450
(2007/10/02)
Synthesis of 5H-Thienopyrrole
5H-Thienopyrrole (4) was synthesized by a novel phosphineimine-alkylidenemalonate cyclization reaction.
Sha, Chin-Kang,Tsou, Chiu-Peng
p. 310 - 311
(2007/10/02)
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