Sornsiri HlekhlaiNatthapol SamakkanadTassaporn SawangphonManat PohmakotrVichai ReutrakulDarunee SoorukramThaworn JaipetchChutima KuhakarnMahidol University2018-11-092018-11-092014-11-01European Journal of Organic Chemistry. Vol.2014, No.33 (2014), 7433-7442109906901434193X2-s2.0-84942001936https://repository.li.mahidol.ac.th/handle/20.500.14594/33610© Copyright 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. Oxone® (2KHSO5·KHSO4·K2SO4) was used to promote the nitration of alkenes and alkynes with sodium nitrite (NaNO2) and potassium iodide (KI). This stable, easy-to-handle, and environmentally benign oxidant was used under mild conditions (room temperature) and provided short reaction times. Styrene derivatives that did not contain electron-donating groups afforded the corresponding nitro alkenes in moderate to good yields, whereas aliphatic alkenes and electron-deficient alkenes were not good substrates. Under similar reaction conditions, aryl alkynes yielded β-iodonitro alkenes. Oxone® (2KHSO5·KHSO4·K2SO4) was used to promote the reactions of alkenes and alkynes with sodium nitrite (NaNO2) and potassium iodide (KI) to afford the corresponding nitro and β-iodonitro-substituted alkenes, respectively, in moderate to good yields.Mahidol UniversityChemistryArticleSCOPUS10.1002/ejoc.201402750