108293-35-2Relevant academic research and scientific papers
Sulfination of alcohols with sodium sulfinates promoted by BF3·OEt2: An unexpected access
Huang, Mingming,Hu, Liangzhen,Shen, Hang,Liu, Qing,Hussain, Muhammad Ijaz,Pan, Jing,Xiong, Yan
supporting information, p. 1874 - 1879 (2016/04/19)
A BF3·OEt2-promoted direct substitution of various alcohols with sodium sulfinates affording sulfinates under mild conditions has been developed. Further reaction of the hydroxysteroids achieves the highly complex sulfinates in good yields, which are two potential pharmacophores routinely encountered in drug discovery.
Preparation and Reactions of Some Cyclic Orthoester Derivatives
Crich, David,Ritchie, Timothy J.
, p. 2319 - 2328 (2007/10/02)
Deprotonation of the alkoxysulphone (5) followed by quenching with diphenyl disulphide yields the dithioorthoester (6) and not the expected ketene monothioacetal (7).Attempts at orthoester exchange of (6) with decanol with a variety of reagents lead to ring opened products.Quenching of the anion derived from (5) with sulphuryl chloride or bromine leads respectively to the chloride (19) and bromide (20).Solvolysis of these halides leads to formation of sulphinate esters.
