An article Cobalt-Catalyzed E-Selective Isomerization of Alkenes with a Phosphine-Amido-Oxazoline Ligand WOS:000537629600045 published article about STEREOSELECTIVE-SYNTHESIS; TRISUBSTITUTED ALKENES; OLEFIN METATHESIS; TERMINAL ALKENES; TRI; PHENYLPROPANOIDS; DERIVATIVES; COMPLEXES; MECHANISM; ALKYNES in [Liu, Hongmei; Cai, Cheng; Ding, Yanghao; Chen, Jianhui; Liu, Bosheng; Xia, Yuanzhi] Wenzhou Univ, Coll Chem & Mat Engn, Wenzhou 325035, Peoples R China in 2020.0, Cited 83.0. Recommanded Product: 500-22-1. The Name is 3-Pyridinecarboxaldehyde. Through research, I have a further understanding and discovery of 500-22-1
An efficient method to access (E)-trisubstituted alkenes is reported via cobalt-catalyzed isomerization of 1,1-disubstituted alkenes using a phosphine-amido-oxazoline ligand. The reaction could also convert mono- and 1,2-disubstituted alkenes to (E)-internal alkenes with benzylic selectivity. This protocol is atom-economy and operationally simple and uses readily available starting materials with good functional tolerance. This catalytic system could be scaled up to gram scale smoothly with a catalyst loading of 0.1 mol %.
Recommanded Product: 500-22-1. Welcome to talk about 500-22-1, If you have any questions, you can contact Liu, HM; Cai, C; Ding, YH; Chen, JH; Liu, BS; Xia, YZ or send Email.
Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem