An efficient metal-free and catalyst-free C�S/C�O bond-formation strategy: synthesis of pyrazole-conjugated thioamides and amides

dc.contributor.authorSharma, Shubham
dc.contributor.authorSingh, Dharmender
dc.contributor.authorKumar, Sunit
dc.contributor.authorVaishali
dc.contributor.authorJamra, Rahul
dc.contributor.authorBanyal, Naveen
dc.contributor.authorDeepika
dc.contributor.authorMalakar, Chandi C.
dc.contributor.authorSingh, Virender
dc.date.accessioned2024-01-21T10:33:07Z
dc.date.accessioned2024-08-13T11:16:19Z
dc.date.available2024-01-21T10:33:07Z
dc.date.available2024-08-13T11:16:19Z
dc.date.issued2023-03-02T00:00:00
dc.description.abstractAn operationally simple and metal-free approach is described for the synthesis of pyrazole-tethered thioamide and amide conjugates. The thioamides were generated by employing a three-component reaction of diverse pyrazole C-3/4/5 carbaldehydes, secondary amines, and elemental sulfur in a single synthetic operation. The advantages of this developed protocol refer to the broad substrate scope, metal-free and easy to perform reaction conditions. Moreover, the pyrazole C-3/5-linked amide conjugates were also synthesized via an oxidative amination of pyrazole carbaldehydes and 2-aminopyridines using hydrogen peroxide as an oxidant. � 2023 Sharma et al.en_US
dc.identifier.doi10.3762/bjoc.19.22
dc.identifier.issn18605397
dc.identifier.urihttps://kr.cup.edu.in/handle/32116/3269
dc.identifier.urlhttps://www.beilstein-journals.org/bjoc/articles/19/22
dc.language.isoen_USen_US
dc.publisherBeilstein-Institut Zur Forderung der Chemischen Wissenschaftenen_US
dc.subjectC�S/O bond formationen_US
dc.subjectmetal-freeen_US
dc.subjectoxidative amidationen_US
dc.subjectpyrazole carbaldehydesen_US
dc.subjectsulfur insertionen_US
dc.subjectthioamidesen_US
dc.titleAn efficient metal-free and catalyst-free C�S/C�O bond-formation strategy: synthesis of pyrazole-conjugated thioamides and amidesen_US
dc.title.journalBeilstein Journal of Organic Chemistryen_US
dc.typeArticleen_US
dc.type.accesstypeOpen Accessen_US

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