127808-49-5Relevant articles and documents
A Commercially Available and User-Friendly Catalyst for Hydroamination Reactions under Technical Conditions
Zelenay, Benjamin,Munton, Peter,Tian, Xiaojie,Díez-González, Silvia
, p. 4725 - 4730 (2019/08/01)
The activity of a simple, commercially available copper salt, [Cu(NCMe)4](BF4) in intramolecular hydroamination reactions of alkynes and allenes is presented. Reactions were successfully carried out in technical acetonitrile in the presence of air. While attempts of alkene hydroamination failed, this catalyst was also found active in intermolecular aza-Michael reactions.
The acid-mediated intramolecular 1,3-dipolar cycloaddition of derived 2-nitro-1,1-ethenediamines for the synthesis of novel fused bicyclic isoxazoles
Page, Lee W.,Bailey, Matthew,Beswick, Paul J.,Frydrych, Simon,Gleave, Robert J.
scheme or table, p. 3388 - 3391 (2010/09/05)
The discovery of a novel synthesis of new fused bicyclic isoxazoles, for example, N-methyl-3-phenyl-5,6-dihydro-4H-isoxazolo[3,4-c]azepin-8-amine (2a), N-methyl-3-phenyl-4,5-dihydroisoxazolo[3,4-c]pyridin-7-amine (2b) and N-methyl-3-phenyl-4H-pyrrolo[3,4-
Synthesis of a bioprobe for elucidation of target molecule of spongean anti-malarial peroxides
Murakami, Nobutoshi,Kawanishi, Motoyuki,Itagaki, Sawako,Horii, Toshihiro,Kobayashi, Motomasa
, p. 3513 - 3516 (2007/10/03)
The reactants of an anti-malarial peroxide having a 6-carbomethoxymethyl-3- methoxy-1,2-dioxane moiety treated with FeSO4 were analyzed. For mechanistic study of the anti-malarial peroxide, two biotinylated probes to elucidate the target molecu
