PhI(OAc)2/KI-mediated reaction of aryl sulfinates with alkenes, alkynes, and α,β-unsaturated carbonyl compounds: Synthesis of vinyl sulfones and β-iodovinyl sulfones

Praewpan KatrunSupanimit ChiampanichayakulKanokwan KorworapanManat PohmakotrVichai ReutrakulThaworn JaipetchChutima KuhakarnMahidol University2018-09-242018-09-242010-10-01European Journal of Organic Chemistry. No.29 (2010), 5633-5641109906901434193X2-s2.0-78249261544https://repository.li.mahidol.ac.th/handle/20.500.14594/28917(Diacetoxyiodo)benzene [PhI(OAc)2, DIB] was able to promote the reaction of sodium aryl sulfinate and potassiumiodide (KI) with alkenes and alkynes to afford the corresponding vinyl sulfones and β-iodovinyl sulfones, respectively, in good yields. The salient features of this reaction are that it employs a commercially available and environmentally benign hypervalent iodine(III) reagent, a one-step reaction, a short reaction time, and mild reaction conditions. (Diacetoxyiodo)benzene/KI was able to promote the reaction of sodium aryl sulfinates with alkenes to afford vinyl sulfones in good yields. Alkynes underwent a similar reaction to give β-iodovinyl sulfones. The present method can be considered to be a convenient and attractive alternative to the existing methods for the synthesis of these intermediates, which are important in organic chemistry. © 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.Mahidol UniversityChemistryPhI(OAc)2/KI-mediated reaction of aryl sulfinates with alkenes, alkynes, and α,β-unsaturated carbonyl compounds: Synthesis of vinyl sulfones and β-iodovinyl sulfonesArticleSCOPUS10.1002/ejoc.201000641