1015198-46-5Relevant articles and documents
Diastereoselective allylation and crotylation of N-tert-butanesulfinyl imines with allylic alcohols
Barros, Olga Soares Do Rego,Sirvent, Juan Alberto,Foubelo, Francisco,Yus, Miguel
, p. 6898 - 6901 (2014)
The palladium-catalyzed allylation of N-tert-butanesulfinyl imines with allylic alcohols in the presence of InI as reducing reagent takes place with high diastereoselectivity in reasonable yields. The reaction with crotyl alcohol is totally regioselective
Multifunctional 1,3-diphenylguanidine for the carboxylative cyclization of homopropargyl amines with CO2 under ambient temperature and pressure
Gao, Xiao-Tong,Xie, Shi-Liang,Zhou, Feng,Wu, Hai-Hong,Zhou, Jian
supporting information, p. 14303 - 14306 (2019/12/03)
Herein, we report that 1,3-diphenylguanidine (DPG) could be utilized for the carboxylative cyclization of homopropargyl amines with CO2 under ambient temperature and pressure, in combination with AgSbF6, which enabled the synthesis o
Synthesis and in vitro antitumor activity of novel iridium(III) complexes with enantiopure C2-symmetrical vicinal diamine ligands
Yang, Qing,Chang, Jun,Song, Jiao,Qian, Meng-Ting,Yu, Jian-Ming,Sun, Xun
, p. 4602 - 4607 (2013/08/23)
Four novel iridium(III) complexes with enantiopure C2- symmetrical vicinal diamine ligands were designed, synthesized, and characterized by FT-IR, NMR, and MS. The cytotoxicities of all of the complexes against the human solid tumor cell lines
