1264737-41-8Relevant articles and documents
Isocyanide-Induced Esterification of Sulfinic Acids to Access Sulfinates
Yang, Jianjing,Dong, Haozhe,Yan, Kelu,Song, Xiaodan,Yu, Jie,Wen, Jiangwei
supporting information, p. 5417 - 5421 (2021/09/29)
The isocyanide-induced esterification of sulfinic acids with alcohols or thiophenols access to sulfinates has been developed. Various primary, secondary, and tertiary alcohols could be compatible with the established protocols. Notably, such an isocyanide-induced synthetic strategy presented the advantages of simple operation, good functional group tolerance, and more than 40 examples up to 99% yields. (Figure presented.).
Preparation method of sulfinate compound
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Paragraph 0039-0042, (2021/02/13)
The invention relates to a preparation method of a sulfinate compound shown as a formula (III), which comprises the following steps: by using a sulfonyl hydrazine compound shown as a formula (I) and alcohol shown as a formula (II) as raw materials, adding
Electrochemical Synthesis of Sulfinic Esters via Aerobic Oxidative Esterification of Thiophenols with Alcohols
Zhou, Hongyan,Duan, Jiaokui,Xie, Dongtai,Yang, Jingya,Ma, Ben,Wang, Ganggang,Wu, Chengqi,Wang, Xi-Cun
, p. 2705 - 2712 (2020/09/15)
A method for the electrochemical synthesis of sulfinic esters by aerobic oxidative coupling of thiophenols and alcohols has been developed. Using electrons as the redox reagent and O 2in air as the oxygen source, the reactions proceeded smoothly at room temperature, even for a gram-scale preparation. No use of catalyst, clean redox reagent, green and abundant oxygen source, and mild reaction conditions make this strategy eco-friendl.
