An efficient method for aromatic Friedel–Crafts alkylation, acylation, benzoylation, and sulfonylation reactions
作者:Ravi P Singh、Rajesh M Kamble、Kusum L Chandra、P Saravanan、Vinod K Singh
DOI:10.1016/s0040-4020(00)01005-x
日期:2001.1
Aromatic electrophilic substitution reactions such as alkylation, acylation, benzoylation, and sulfonylation were studied in the presence of a catalytic amount of Cu(OTf)2 and Sn(OTf)2. Cu(OTf)2 was very efficient for alkylation, acylation, and benzoylation reactions. However, in case of sulfonylation reactions, Sn(OTf)2 gave better results.
Selective Synthesis of <i>ortho-</i>Substituted Diarylsulfones by Using NHC-Au Catalysts under Mild Conditions
作者:Haibo Zhu、Yajing Shen、Daheng Wen、Zhang-Gao Le、Tao Tu
DOI:10.1021/acs.orglett.8b03957
日期:2019.2.15
A single-step gold(I)-catalyzed chemoselective protocol to access ortho-substituted diarylsulfones has been established. Acenaphthoimidazolylidene gold complexes are effective catalysts for the arylsulfonylation of boronic acids by potassium metabisulfite (K2S2O5) and diaryliodonium salts to access (poly-)ortho-substituted diarylsulfones even in gram scale. Unlike the transition metal-catalyzed two-component
已经建立了一步金(I)催化的化学选择方案以访问邻位取代的二芳基砜。ena啶咪唑基亚金络合物是焦亚硫酸氢钾(K 2 S 2 O 5)和二芳基碘鎓盐对硼酸进行芳基磺酰化的有效催化剂,即使以克为单位,也可得到(多)邻位取代的二芳基砜。与过渡金属催化的双组分偶联系统不同,二芳基碘鎓盐中的位阻芳基优先转移到体积较小的芳基上,以形成合成困难的靶标,包括具有药学重要性的靶标。
Acylation and Related Reactions under Microwaves. 4. Sulfonylation Reactions of Aromatics
reactive and/or nonvolatile reagents (anisole, xylenes, mesitylene) expeditious conditions (short reaction time at constant MW power without control of the temperature) were used. With less reactive and/or low-boiling reagents (benzene, toluene, halobenzenes), the rise in temperature and the increase of reaction time were controlled either by sequential MW irradiation or by a temperature order. It was shown
作者:Edward J. Emmett、Barry R. Hayter、Michael C. Willis
DOI:10.1002/anie.201305369
日期:2013.11.25
SO(2) efficient: A three‐component palladium‐catalyzed coupling of aryl lithium compounds; sulfurdioxide (provided by the easy‐to‐handle solid surrogate, DABSO); and aryl, heteroaryl, and alkenyl (pseudo)halides yields a diverse library of sulfones. An electron‐poor XantPhos‐type ligand suppresses aryl–aryl exchange and is key to obtaining high yields.
Aryldiazonium Salts and DABSO: A Versatile Combination for Three‐Component Sulfonylative Cross‐Coupling Reactions
作者:Pritha Das、Subhodeep Das、Ranjan Jana
DOI:10.1002/asia.202200085
日期:2022.6
A catalyzed synthesis of diarylsulfones with arylboronic acids and catalyst-free synthesis of arylvinyl and alkylvinyl sulfonesfromvinyl bronic acids or halides is reported.