386758-32-3Relevant academic research and scientific papers
A tandem Heck-aza-Michael addition protocol for the one-pot synthesis of isoindolines from unprotected amines
Chen, Ke,Pullarkat, Sumod A.
experimental part, p. 6600 - 6606 (2012/09/08)
A palladacycle-catalyzed tandem Heck-intramolecular aza-Michael reaction protocol has been developed for the one-pot synthesis of 1-substituted isoindolines from N-unprotected 2-bromobenzylamines and acrylates with high yields.
Consecutive condensation, C-N and N-N bond formations: A copper-catalyzed one-pot three-component synthesis of 2 H -indazole
Kumar, Manian Rajesh,Park, Ahbyeol,Park, Namjin,Lee, Sunwoo
supporting information; experimental part, p. 3542 - 3545 (2011/09/12)
2H-Indazoles are synthesized using copper-catalyzed, one-pot, three-component reactions of 2-bromobenzaldehydes, primary amines, and sodium azide. A copper catalyst plays the key role in the formation of C-N and N-N bonds. This method has a broad substrate scope with a high tolerance for a variety of functional groups.
