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

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.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.identifier.doi 10.1039/d0ra04255b
dc.identifier.issn 2046-2069
dc.identifier.scopus 2-s2.0-85093700687
dc.identifier.uri https://doi.org/10.1039/d0ra04255b
dc.identifier.uri https://hdl.handle.net/20.500.14720/6960
dc.language.iso en en_US
dc.publisher Royal Soc Chemistry 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
dspace.entity.type Publication
gdc.author.id Ebadi, Dr. Abdol Ghaffar/0000-0003-4472-5866
gdc.author.id Mert, Nihat/0000-0001-7185-3316
gdc.author.id Vessally, Esmail/0000-0002-6465-7605
gdc.author.id Toughani, Mohsen/0000-0001-9437-0114
gdc.author.scopusid 59624726300
gdc.author.scopusid 55408378200
gdc.author.scopusid 57216693356
gdc.author.scopusid 6601956926
gdc.author.scopusid 22982172500
gdc.author.wosid Ebadi, Abdol/Aav-9463-2021
gdc.author.wosid Mert, Nihat/Hjh-5486-2023
gdc.coar.access open access
gdc.coar.type text::journal::journal article
gdc.description.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
gdc.description.departmenttemp [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
gdc.description.endpage 37313 en_US
gdc.description.issue 61 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q1
gdc.description.startpage 37299 en_US
gdc.description.volume 10 en_US
gdc.description.woscitationindex Science Citation Index Expanded
gdc.description.wosquality Q2
gdc.identifier.pmid 35521237
gdc.identifier.wos WOS:000578727600037
gdc.index.type WoS
gdc.index.type Scopus
gdc.index.type PubMed

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