Gelişmiş Arama

Basit öğe kaydını göster

dc.contributor.authorKaniskan, Nevin
dc.contributor.authorKökten, Şule
dc.contributor.authorÇelik, İlhami
dc.date.accessioned2019-10-20T09:13:28Z
dc.date.available2019-10-20T09:13:28Z
dc.date.issued2012
dc.identifier.issn1551-7004
dc.identifier.issn1551-7012
dc.identifier.urihttps://hdl.handle.net/11421/16924
dc.descriptionWOS: 000313583500018en_US
dc.description.abstractA convenient route for efficient conversion of unprotected anthranilic acids into the corresponding N-(2-aminoarylacyl)benzotrazoles is described. N-(2-Aminoarylacyl)benzotrazoles have been successfully used to synthesize primary, secondary and tertiary anthranilamides in high yields (71-96%).en_US
dc.description.sponsorshipAnadolu University [1002F88]en_US
dc.description.sponsorshipThis work is dedicated to Professor Cemil Ogretir, who died on 19th January, 2011. It is gratefully acknowledged that this work was supported financially by Anadolu University (Project No: 1002F88) and we are also grateful to AUBIBAM for providing <SUP>1</SUP>H and <SUP>13</SUP>C NMR spectra.en_US
dc.language.isoengen_US
dc.publisherArkat Usa Incen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAnthranilic Aciden_US
dc.subjectBenzotriazoleen_US
dc.subjectN-(2-Aminoarylacyl)Benzotrazolesen_US
dc.subjectAnthranilamidesen_US
dc.titleA new protocol for the synthesis of primary, secondary and tertiary anthranilamides utilizing N-(2-aminoarylacyl)benzotriazolesen_US
dc.typearticleen_US
dc.relation.journalArkivocen_US
dc.contributor.departmentAnadolu Üniversitesi, Fen Fakültesi, Fizik Bölümüen_US
dc.identifier.startpage198en_US
dc.identifier.endpage213en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.contributor.institutionauthorÇelik, İlhami


Bu öğenin dosyaları:

DosyalarBoyutBiçimGöster

Bu öğe ile ilişkili dosya yok.

Bu öğe aşağıdaki koleksiyon(lar)da görünmektedir.

Basit öğe kaydını göster