Ecofriendly Synthesis in Aqueous Medium: An Expeditious Approach to New N,N-Diethyl Amide Bearing Benzenemethanesulfonamides

dc.contributor.authorAjani, O.O.
dc.contributor.authorFamiloni, O.B.
dc.contributor.authorEcheme, J.O.
dc.contributor.authorWu, F.
dc.date.accessioned2019-09-05T09:53:02Z
dc.date.available2019-09-05T09:53:02Z
dc.date.issued2013-12
dc.description.abstractAn highly expeditious synthetic approach for the synthesis of benzenemethanesulfonamides (1a-k) and their new corresponding N,N-diethyl substituted amido moieties (2a-k) has been achieved in aqueous medium at room temperature. The reaction condition was thoroughly optimized thereby allowing significant rate enhancement and resulting into excellent yields. The chemical structures of the successful candidates were confirmed using elemental analytical and spectroscopic data such as IR, 1 H NMR, 13C NMR and some selected mass spectral data.en_US
dc.identifier.citationAjani, O. O., Familoni, O. B., Echeme, J. O., & Wu, F. (2013). Ecofriendly Synthesis in Aqueous Medium: An Expeditious Approach to New N, N-Diethyl Amide Bearing Benzenemethanesulfonamides. The Open Organic Chemistry Journal, 7, 1-10.en_US
dc.identifier.urihttps://ir.unilag.edu.ng/handle/123456789/5160
dc.language.isoenen_US
dc.publishereprints.covenantuniversity.edu.ngen_US
dc.subjectResearch Subject Categories::NATURAL SCIENCES::Chemistry::Organic chemistry::Organic synthesisen_US
dc.subjectsulfonamideen_US
dc.subjectamino acidsen_US
dc.subjectspectroscopyen_US
dc.subjectsulfonylationen_US
dc.titleEcofriendly Synthesis in Aqueous Medium: An Expeditious Approach to New N,N-Diethyl Amide Bearing Benzenemethanesulfonamidesen_US
dc.typeArticleen_US
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