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dc.contributor.authorKhayitov, Jonibek
dc.contributor.authorYuldashev, Tashmurza Rakhmonovich
dc.contributor.authorBuronov, Firdavsiy Eshburiyevich
dc.contributor.authorIsmailov, Boburbek Mahmudjanovich
dc.contributor.authorRakhimov, Khusniddin
dc.contributor.authorBobomuradov, Utkir Ziyadullayevich
dc.contributor.authorAvlayarova, Nargiza Maxmudovna
dc.contributor.authorYunusov, Khaydar E.
dc.date.accessioned2025-10-17T08:26:28Z
dc.date.available2025-10-17T08:26:28Z
dc.date.issued2024-07
dc.identifier.issn(print) 2676-7279
dc.identifier.urihttps://dspace.kstu.uz/xmlui/handle/123456789/541
dc.description.abstractThioesters are a class of highly useful compounds in synthetic chemistry, and many thioester compounds show biological and pharmacological activities. Organic halides and thiols are widely accessible chemical feedstocks and are widely used in industry as building blocks. The synthesis of thioesters from these basic chemicals is important for chemical synthesis nowadays. Over the years, many efforts have been made to access thioester derivatives through thiocarbonylation of organic halides with thiols using different carbon monoxide sources including CO, CO2, COgen, [CpFe(CO)2]2, Cr(CO)6, etc. Herein, we summarize the recent advances of these carbonylative coupling reactions.en_US
dc.language.isoenen_US
dc.publisherChemical Review and Lettersen_US
dc.relation.ispartofseries2645-4947;(print) 2676-7279
dc.subjectCarbonylative coupling reactionsen_US
dc.subjectThioestersen_US
dc.subjectOrganic halidesen_US
dc.subjectThiolsen_US
dc.subjectPalladium catalystsen_US
dc.titleTransition metal-catalyzed carbonylative coupling of aryl/alkyl halides with thiols: A straightforward synthesis of thioester derivativesen_US
dc.typeArticleen_US


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