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Direct Sulfonamidation of (Hetero)aromatic C-H Bonds With Sulfonyl Azides: a Novel and Efficient Route Ton-(hetero)aryl Sulfonamides

dc.authorid Ebadi, Dr. Abdol Ghaffar/0000-0003-4472-5866
dc.authorid Mert, Nihat/0000-0001-7185-3316
dc.authorid Vessally, Esmail/0000-0002-6465-7605
dc.authorid Toughani, Mohsen/0000-0001-9437-0114
dc.authorscopusid 59624726300
dc.authorscopusid 55408378200
dc.authorscopusid 57216693356
dc.authorscopusid 6601956926
dc.authorscopusid 22982172500
dc.authorwosid Ebadi, Abdol/Aav-9463-2021
dc.authorwosid Mert, Nihat/Hjh-5486-2023
dc.contributor.author Liu, Zhi
dc.contributor.author Ebadi, Abdolghaffar
dc.contributor.author Toughani, Mohsen
dc.contributor.author Mert, Nihat
dc.contributor.author Vessally, Esmail
dc.date.accessioned 2025-05-10T17:08:03Z
dc.date.available 2025-05-10T17:08:03Z
dc.date.issued 2020
dc.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
dc.department-temp [Liu, Zhi] East China Jiaotong Univ, Sch Elect & Automat Engn, Nanchang 330013, Jiangxi, Peoples R China; [Ebadi, Abdolghaffar] Islamic Azad Univ, Jouybar Branch, Dept Agr, Jouybar, Iran; [Toughani, Mohsen; Vessally, Esmail] Islamic Azad Univ, Babol Branch, Dept Fishery, Babol, Iran; [Mert, Nihat] Yuzuncu Yil Univ, Fac Vet Med, Dept Biochem, TR-65080 Van, Turkey; Payame Noor Univ, Dept Chem, Tehran, Iran en_US
dc.description Ebadi, Dr. Abdol Ghaffar/0000-0003-4472-5866; Mert, Nihat/0000-0001-7185-3316; Vessally, Esmail/0000-0002-6465-7605; Toughani, Mohsen/0000-0001-9437-0114 en_US
dc.description.abstract N-Aryl sulfonamides belong to a highly important class of organosulfur compounds which are found in a number of FDA-approved drugs such as dofetilide, dronedarone, ibutilide, sotalol, sulfadiazine, sulfamethizole, vemurafenib, and many more. There is therefore continuing interest in the development of novel and convenient protocols for the preparation of these pharmaceutically important compounds. Recently, direct sulfonamidation of (hetero)aromatic C-H bonds with easily available sulfonyl azides has emerged as an attractive and powerful strategy to accessN-(hetero)aryl sulfonamides where non-toxic nitrogen gas forms as the sole by-product. This review highlights recent advances and developments (2012-2020) in this fast growing research area with emphasis on the mechanistic features of the reactions. en_US
dc.description.woscitationindex Science Citation Index Expanded
dc.identifier.doi 10.1039/d0ra04255b
dc.identifier.endpage 37313 en_US
dc.identifier.issn 2046-2069
dc.identifier.issue 61 en_US
dc.identifier.pmid 35521237
dc.identifier.scopus 2-s2.0-85093700687
dc.identifier.scopusquality Q1
dc.identifier.startpage 37299 en_US
dc.identifier.uri https://doi.org/10.1039/d0ra04255b
dc.identifier.uri https://hdl.handle.net/20.500.14720/6960
dc.identifier.volume 10 en_US
dc.identifier.wos WOS:000578727600037
dc.identifier.wosquality Q2
dc.language.iso en en_US
dc.publisher Royal Soc Chemistry en_US
dc.relation.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.title Direct Sulfonamidation of (Hetero)aromatic C-H Bonds With Sulfonyl Azides: a Novel and Efficient Route Ton-(hetero)aryl Sulfonamides en_US
dc.type Article en_US

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