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dc.contributor.authorKatritzky, Alan R.
dc.contributor.authorAbdel-Fattah, Ashraf A. A.
dc.contributor.authorÇelik, İlhami
dc.date.accessioned2019-10-20T09:03:11Z
dc.date.available2019-10-20T09:03:11Z
dc.date.issued2007
dc.identifier.issn1551-7004
dc.identifier.issn1551-7012
dc.identifier.urihttps://dx.doi.org/10.3998/ark.5550190.0008.b09
dc.identifier.urihttps://hdl.handle.net/11421/16651
dc.descriptionWOS: 000251573700010en_US
dc.description.abstractReactions of readily available and stable N-(alpha-amidoalkyl)benzotriazoles 1 ( derived from a variety of aliphatic, aromatic or heterocyclic aldehydes) with diverse nitroalkanes, nitriles, alkynes and esters afforded N-(beta-nitroalkyl) amides 4 (54-96%), N-(beta-cyanoalkyl) amides 6 (58-88%), N- acylpropargylamines 11 (41-87%) and esters of beta-N-acylamino acids 13 (68-96%), respectively.en_US
dc.language.isoengen_US
dc.publisherArkat Usa Incen_US
dc.relation.isversionof10.3998/ark.5550190.0008.b09en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAmidoalkylationen_US
dc.subjectN-(Beta-Nitroalkyl) Amidesen_US
dc.subjectN-(Beta-Cyanoalkyl)-Amidesen_US
dc.subjectN-Acylpropargylaminesen_US
dc.subjectBeta-N-Acylamino Acidsen_US
dc.titleBenzotriazole-mediated amidoalkylations of nitroalkanes, nitriles, alkynes and estersen_US
dc.typearticleen_US
dc.relation.journalArkivocen_US
dc.contributor.departmentAnadolu Üniversitesi, Fen Fakültesi, Fizik Bölümüen_US
dc.identifier.startpage96en_US
dc.identifier.endpage113en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.contributor.institutionauthorÇelik, İlhami


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