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dc.contributor.authorFernández Peña, Laura 
dc.contributor.authorGonzález-Andrés, Paula 
dc.contributor.authorBarbero, Asunción
dc.date.accessioned2025-07-04T17:00:32Z
dc.date.available2025-07-04T17:00:32Z
dc.date.issued2024
dc.identifier.citationRSC Adv., 2024, 14, 707–711es
dc.identifier.urihttps://uvadoc.uva.es/handle/10324/76255
dc.description.abstractWe herein present a selective methodology for the synthesis of disubstituted dihydropyrans by silyl-Prins cyclization of Z-vinylsilyl alcohols mediated by trimethylsilyl trifluoromethanesulfonate (TMSOTf). The reaction features broad substrate scope, short reaction times and ease of process scale-up. Moreover, to showcase the applicability of the proposed method, we also report a facile and linear synthesis of analogues of rhopaloic acid and natural doremox fragrance.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenges
dc.publisherRSCes
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.titleTowards an efficient methodology for the synthesis of functionalized dihydropyrans by silyl-Prins cyclization: access to truncated natural productses
dc.typeinfo:eu-repo/semantics/articlees
dc.identifier.doihttps://doi.org/10.1039/d3ra07520fes
dc.identifier.publicationfirstpage707es
dc.identifier.publicationlastpage711es
dc.identifier.publicationtitleTowards an efficient methodology for the synthesis of functionalized dihydropyrans by silyl-Prinses
dc.identifier.publicationvolume14es
dc.peerreviewedSIes
dc.type.hasVersioninfo:eu-repo/semantics/draftes


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