856118-83-7Relevant academic research and scientific papers
Tandem one-pot synthesis of polysubstituted NH-pyrroles involving the palladium-catalyzed intramolecular oxidative amination of the zinc bromide complex of β-enamino esters
Kim, Ju Hyun,Choi, Suh Young,Bouffard, Jean,Lee, Sang-Gi
, p. 9253 - 9261 (2014)
The Pd-catalyzed oxidative olefin amination of the zinc bromide complex intermediate, formed by the sequential reaction of nitriles with a Reformatsky reagent and 1-alkynes, affords pyrrole derivatives in good to excellent yields. This tandem protocol pro
Reaction of functionalized azomethine ylides with acetylenic dipolarophiles: the facile synthesis of functionalized 2H- and 1H-pyrroles
Kawashima, Keisuke,Hiromoto, Masanori,Hayashi, Kyohei,Kakehi, Akikazu,Shiro, Motoo,Noguchi, Michihiko
, p. 941 - 944 (2008/02/04)
The reaction of functionalized azomethine ylides as C-unsubstituted nitrile ylide equivalents with acetylenic dipolarophiles is mentioned. Therein, the initially formed cycloadducts, 2,5-dihydropyrroles, by the reaction of the azomethine ylides with subst
