A method for the electrochemical synthesis of sulfinic esters by aerobicoxidative coupling of thiophenols and alcohols has been developed. Using electrons as the redox reagent and O2 in 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
We have developed a protocol for the NaHSO3‐promoted esterification of sulfonyl hydrazides with alcohols for the synthesis of sulfinicesters. Various sulfonyl hydrazides could be converted to the corresponding sulfinicesters in good to high yields. The merits of this protocol include mild transition‐metal‐free reaction conditions, an inexpensive and available reagent, and operational simplicity.
Here, we developed a new cobalt nanocatalyst supported on N–SiO2-doped activated carbon (Co/N–SiO2–AC), which exhibits excellent catalytic performance towards the oxidative esterification of (hetero)aryl and alkyl thiols with alcohols. A wide array of sulfinic esters were efficiently afforded in an exclusive chemoselective manner. The developed synthetic method proceeds with the merits of mild reaction
Palladium-Catalyzed Sulfinylation of Aryl- and Alkenylborons with Sulfinate Esters
作者:Minori Suzuki、Kazuya Kanemoto、Yu Nakamura、Takamitsu Hosoya、Suguru Yoshida
DOI:10.1021/acs.orglett.1c01292
日期:2021.5.7
An efficient, direct sulfinylation of organoborons catalyzed by palladium is disclosed. Treatment of organoborons and sulfinate esters in the presence of a palladium precatalyst provided a broad range of sulfoxides. Various organosulfur compounds having oxidizable functional groups were successfully prepared through the sulfoxide synthesis.
An efficient and eco-friendly electrochemical synthesis of various sulfinic esters from thiols and alcohols via sequential S–H/S bond cleavage and double S–O bond formation under mild reaction conditions has been developed. Stoichiometric oxidants, metal catalysts, activating agents and even added bases were avoided in this method, and the only by-product generated from this reaction was dihydrogen