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Iodine-catalyzed oxidative amination of sodium sulfinates: A convenient approach to the synthesis of sulfonamides under mild conditions

dc.contributor.authorChonchanok Buathongjanen_US
dc.contributor.authorDanupat Beukeawen_US
dc.contributor.authorSirilata Yotphanen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-11-23T09:58:33Z
dc.date.available2018-11-23T09:58:33Z
dc.date.issued2015-01-01en_US
dc.description.abstract© 2015 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim. The iodine-catalyzed oxidative amination of sodium sulfinates in the presence of sodium percarbonate as the oxidant has been developed. The reaction shows good substrate scope and tolerates a wide range of functionalities in both amine and sodium sulfinate substrates. Aliphatic amines, heteroaromatic amines and hydrochloride salts of amines canbe employed as the amine sources in this transformation. Mechanistic studies indicated that a radical pathway might be involved in the reaction process. This transition-metalfree protocol offers an alternative and convenient approach for a preparation of a series of sulfonamides in moderate to good yields under mild conditions.en_US
dc.identifier.citationEuropean Journal of Organic Chemistry. Vol.2015, No.7 (2015), 1575-1582en_US
dc.identifier.doi10.1002/ejoc.201403531en_US
dc.identifier.issn10990690en_US
dc.identifier.issn1434193Xen_US
dc.identifier.other2-s2.0-85027934131en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/35766
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85027934131&origin=inwarden_US
dc.subjectChemistryen_US
dc.titleIodine-catalyzed oxidative amination of sodium sulfinates: A convenient approach to the synthesis of sulfonamides under mild conditionsen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85027934131&origin=inwarden_US

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