Synthesis of tetrasubstituted thiophenes starting from amino mercaptoacrylates and α-brominated acetamides

dc.contributor.authorSuarez J.A.Q.
dc.contributor.authorRicardo A.P.
dc.contributor.authorCosta J.M.F.
dc.contributor.authorGoncalves C.P.
dc.contributor.authorTremante M.A.
dc.contributor.authorSaavedra M.S.A.
dc.date.accessioned2024-03-12T19:21:05Z
dc.date.available2024-03-12T19:21:05Z
dc.date.issued2021
dc.description.abstract© 2021 Bentham Science Publishers.Some thiophenic derivatives show important biological activity or are used as intermediates in organic synthesis. For this reason, it is very important to develop new synthesis procedures with good yields and using few synthesis steps. The present work offers an overview of the method for obtaining substituted thiophenes reported in the literature, and the synthetic procedures used from push-pull systems. In this work, we present the synthesis of 14 new tetrasubstituted thiophenes starting from amino mercaptoacrylates and α-brominated acetamides, derived from furoyl and benzoylacetonitrile, respectively. Best yields (66 to 85%) were obtained through ultrasonic irradiation. Combined use of spectroscopic methods and elementary analysis was done for characterization of all the compounds.
dc.description.firstpage748
dc.description.issuenumber6
dc.description.lastpage756
dc.description.volume25
dc.identifier.doi10.2174/1385272825666210111112449
dc.identifier.issn1385-2728
dc.identifier.urihttps://dspace.mackenzie.br/handle/10899/34692
dc.relation.ispartofCurrent Organic Chemistry
dc.rightsAcesso Aberto
dc.subject.otherlanguageAmino mercaptoacrylates salts
dc.subject.otherlanguageAroylacetonitriles
dc.subject.otherlanguagePush-pull
dc.subject.otherlanguageThiophenes
dc.subject.otherlanguageα-brominated acetamides
dc.titleSynthesis of tetrasubstituted thiophenes starting from amino mercaptoacrylates and α-brominated acetamides
dc.typeArtigo
local.scopus.citations5
local.scopus.eid2-s2.0-85116030267
local.scopus.updated2024-12-01
local.scopus.urlhttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85116030267&origin=inward
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