87228-63-5Relevant academic research and scientific papers
Iodine-DMSO-promoted divergent reactivities of arylacetylenes
Rather, Suhail A.,Kumar, Atul,Ahmed, Qazi Naveed
supporting information, p. 4511 - 4514 (2019/04/26)
An unprecedented set of efficient, economical, atom-economic and exceedingly selective I2-DMSO-promoted methods is described for the generation of different structures. The reaction represents the first of its kind, involving the use of different iodine concentrations, temperatures, acids and salt to adjust the selectivity for the synthesis of different alkenes, α-functionalized ketones and α-ketomethylthioesters.
Oxidative Thioesterification of Alkenes Mediated by 1,3-Dibromo-5,5-dimethylhydantoin and DMSO for the Synthesis of α-Ketothioesters
Hua, Jiawei,Xu, Jiaqi,Xu, Jia,Zhou, Bochao,Zhang, Dong,Yang, Zhao,Fang, Zheng,Guo, Kai
, p. 4056 - 4060 (2019/07/03)
A simple and mild approach for the synthesis of α-ketothioesters via 1,3-Dibromo-5,5-dimethylhydantoin (DBH)/DMSO mediated oxidative thioesterification of alkenes has been developed. Various of α-ketothioesters products were produced in moderate to good y
UTILIZATION OF METHYLTHIOMETHYL p-TOLYL SULFONE IN ORGANIC SYNTHESIS
Ogura, Katsuyuki,Yahata, Nobuhiro,Hashizume, Kimitoshi,Tsuyama, Koichi,Takahashi, Kazumasa,Iida, Hirotada
, p. 767 - 770 (2007/10/02)
Methylthiomethyl p-tolyl sulfone was found to be one of the useful reagents for preparation of various organic compounds such as S-methyl α-ketocarbothioates, carboxylic esters, five- and six-membered cycloalkanones, and α-methoxy-α-arylacetic esters.
