ONE-POT AND SIMPLE REACTION FOR THE SYNTHESIS OF ALKYL p-TOLUENESULFINATE ESTERS UNDER SOLID-PHASE CONDITIONS
摘要:
A manipulatively one-pot and rapid method for the synthesis of alkyl p-toluenesulfinate esters 1 from p-toluenesulfinic acid, supported thionyl chloride on silica gel and aliphatic alcohols in solid phase conditions is described.
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
synthesis of cyclicsulfinates and sulfinamides based on intramolecular homolyticsubstitution (SHi) at the sulfuratom by aryl or alkyl radicals is described. Both alkyl and benzofused compounds can be accessed directly from easily prepared acyclic precursors. Enantiomerically enriched sulfur‐based heterocycles were formed through an SHi process with inversion of configuration at the sulfuratom. Cyclization
描述了基于在硫原子上被芳基或烷基自由基的分子内均质取代(S H i)合成环状亚磺酸酯和亚磺酰胺的通用且有效的方法。烷基和苯并稠合的化合物都可以直接从容易制备的无环前体中获得。对映体富集的硫基杂环是通过S H i过程形成的,硫原子上的构型反转。前手性自由基的环化进行的立体化学结果各不相同,具体取决于传入自由基的大小。2-吡啶基和2-喹啉基会生成联芳基化合物,这是由于攻击芳基亚磺酸盐的邻位而不是亲硫取代引起的。
作者:Charlotte S. Richards-Taylor、David C. Blakemore、Michael C. Willis
DOI:10.1039/c3sc52332b
日期:——
electrophilic coupling partner, such as a benzylic, allylic or alkyl halide, an electron-poor arene, or a cyclic epoxide, to provide the corresponding sulfone products in good to excellent yields. The mild reaction conditions and use of commercially available reaction components allows the easy preparation of a broad range of sulfones featuring a variety of functional groups. The process obviates the need
Direct synthesis of sulfinic esters via ultrasound accelerated tandem reaction of thiols and alcohols with <i>N</i>-bromosuccinimide
作者:Lan-Anh Thi Nguyen、Tri-Nghia Le、Cong-Thang Duong、Chi-Tam Vo、Fritz Duus、Thi Xuan Thi Luu
DOI:10.1080/17415993.2021.1928669
日期:2021.9.3
The direct transformation of various thiols and simple alcohols with N-bromosuccinimide into sulfinic esters has been investigated by using different categories of base/acidic catalysts as well as co-solvents under varied reaction conditions. The reaction was found out to afford the sulfinic esters with high yields in the absence of catalysts, especially within the shorter time under the acceleration
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