112238-67-2Relevant academic research and scientific papers
Electrochemical Difunctionalization of Olefines: Access to Selenomethyl-Substituted Cyclic Ethers or Lactones
Meng, Xiu-Jin,Zhong, Ping-Fu,Wang, Yu-Mei,Wang, Heng-Shan,Tang, Hai-Tao,Pan, Ying-Ming
, p. 506 - 511 (2020)
A metal- and oxidant-free electrochemical method for preparing selenomethyl-substituted cyclic ethers or lactones via difunctionalization of olefines is presented. A series of selenomethyl-substituted cyclic ethers, particularly 9- and 11- membered, selen
Preparation of Heterocycles via Visible-Light-Driven Aerobic Selenation of Olefins with Diselenides
Zhang, Qing-Bao,Yuan, Pan-Feng,Kai, Liang-Lin,Liu, Kai,Ban, Yong-Liang,Wang, Xue-Yang,Wu, Li-Zhu,Liu, Qiang
supporting information, p. 885 - 889 (2019/02/14)
The aerobic dehydrogenative cyclization of alkenes with easily accessible diselenides facilitated by visible light is reported. Notably, the features of this transition-metal-free protocol are pronounced efficiency and practicality, good functional group
PHENYLSELENO-LACTONIZATION OF OLEFINIC NITRILES PROMOTED BY PEROXYDISULPHATE ION OXIDATION OF DIPHENYL DISELENIDE
Tiecco, Marcello,Testaferri, Lorenzo,Tingoli, Marco,Bartoli, Donatella
, p. 6819 - 6832 (2007/10/02)
The oxidation of diphenyl diselenide with ammonium peroxydisulphate is a very simple and efficient method to produce phenylselenium cations in the absence of nucleophilic counter ions.The reaction carried out in the presence of an olefin, in acetonitrile
Stereoselective Selenolactonization by Superelectrophilic Benzeneselenenyl Triflate
Murata, Shizuaki,Suzuki, Toshiyasu
, p. 849 - 852 (2007/10/02)
Benzeneselenenyl triflate is prepared from benzeneselenenyl chloride and silver trifluoromethanesulfonate.It performs selenium-induced cyclization of β,γ-, γ,δ-, and δ,ε-unsaturated carboxylic acids.
