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Gold-Catalyzed Oxime-Oxime Rearrangement

dc.authorid Menges, Nurettin/0000-0002-5990-6275
dc.authorscopusid 57204732269
dc.authorscopusid 36872923100
dc.authorscopusid 56673662600
dc.authorscopusid 23973608700
dc.authorscopusid 7006382595
dc.authorwosid Kaya, Serdal/P-3609-2018
dc.authorwosid Guven, Sinem/P-3273-2019
dc.authorwosid Menges, Nurettin/F-9678-2016
dc.contributor.author Guven, Sinem
dc.contributor.author Ozer, Merve Sinem
dc.contributor.author Kaya, Serdal
dc.contributor.author Menges, Nurettin
dc.contributor.author Balci, Metin
dc.date.accessioned 2025-05-10T17:37:39Z
dc.date.available 2025-05-10T17:37:39Z
dc.date.issued 2015
dc.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
dc.department-temp [Guven, Sinem; Ozer, Merve Sinem; Kaya, Serdal; Menges, Nurettin; Balci, Metin] Middle E Tech Univ, Dept Chem, TR-06800 Ankara, Turkey; [Kaya, Serdal] Giresun Univ, Dept Chem, TR-28200 Giresun, Turkey; [Menges, Nurettin] Yuzuncu Yil Univ, Fac Pharm, TR-65100 Van, Turkey en_US
dc.description Menges, Nurettin/0000-0002-5990-6275 en_US
dc.description.abstract The gold-catalyzed reaction of pyrrole and indole oximes having a propargyl group attached to the nitrogen atom was studied. The selective 6-endo-dig mode of cyclization was observed for the terminal alkynes giving rise to the formation of pyrazine N-oxides in the presence of a gold catalyst. However, the reaction with substituted alkyne transferred the oxime functionality intramolecularly from one carbon atom to another via the 7-endo-dig cyclization process. This transformation is unprecedented in the literature and is named an oximeoxime rearrangement. en_US
dc.description.sponsorship Scientific and Technological Research Council of Turkey (TUBITAK) [TBAG-112 T360]; Turkish Academy of Sciences (TUBA); Middle East Technical University (METU) en_US
dc.description.sponsorship Financial support from the Scientific and Technological Research Council of Turkey (TUBITAK, Grant No. TBAG-112 T360), the Turkish Academy of Sciences (TUBA), and Middle East Technical University (METU) is gratefully acknowledged. We also thank Research Assistant Ozlem Sari (METU) for her help with calculations. en_US
dc.description.woscitationindex Science Citation Index Expanded - Index Chemicus - Current Chemical Reactions
dc.identifier.doi 10.1021/acs.orglett.5b01041
dc.identifier.endpage 2663 en_US
dc.identifier.issn 1523-7060
dc.identifier.issn 1523-7052
dc.identifier.issue 11 en_US
dc.identifier.pmid 25992473
dc.identifier.scopus 2-s2.0-84930633059
dc.identifier.scopusquality Q1
dc.identifier.startpage 2660 en_US
dc.identifier.uri https://doi.org/10.1021/acs.orglett.5b01041
dc.identifier.uri https://hdl.handle.net/20.500.14720/14438
dc.identifier.volume 17 en_US
dc.identifier.wos WOS:000355962200025
dc.identifier.wosquality Q1
dc.language.iso en en_US
dc.publisher Amer Chemical Soc en_US
dc.relation.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.title Gold-Catalyzed Oxime-Oxime Rearrangement en_US
dc.type Article en_US

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