1372625-06-3Relevant academic research and scientific papers
Palladium-catalyzed cycloaddition of alkynyl aryl ethers with internal alkynes via selective ortho C-H activation
Minami, Yasunori,Shiraishi, Yuki,Yamada, Kotomi,Hiyama, Tamejiro
, p. 6124 - 6127 (2012/05/07)
Alkynyl aryl ethers react with internal alkynes through selective ortho C-H activation by a palladium(0) catalyst to give substituted 2-methylidene-2H- chromenes. The alkynoxy group acts as a directing group to promote ortho C-H functionalization. Deuterium-labeling experiments indicated that the arylpalladium hydride complex is a key intermediate via oxidative addition. Various functional groups tolerate the present transformation to give the corresponding products.
