dc.contributor.author
Pugnal, Lucas V. B. L.
dc.contributor.author
Vega, Kimberly B.
dc.contributor.author
Pissinati, Emanuele F.
dc.contributor.author
Correia, José Tiago M.
dc.contributor.author
Zukerman-Schpector, Julio
dc.contributor.author
Martin, Ruben
dc.contributor.author
Paixão, Márcio W.
dc.date.accessioned
2023-06-29T13:31:06Z
dc.date.accessioned
2024-04-23T10:15:21Z
dc.date.available
2024-12-04T23:45:11Z
dc.date.issued
2023-05-25
dc.identifier.uri
http://hdl.handle.net/2072/535774
dc.description.abstract
A dual photocatalytic sulfonylation-arylation of electron-rich alkenes is described. By combining sulfinate salts, (hetero)-aryl-bromides and 2,3-dihydrofuran under Ru and Ni dual catalysis, over 35 examples of aryl-sulfonylated scaffolds could be obtained in good to excellent yields, under mild reaction conditions and high diastereoselectivity.
eng
dc.format.extent
6 p.
cat
dc.publisher
Wiley-VCH
cat
dc.rights
Creative Commons. Attribution-NonCommercial
dc.source
RECERCAT (Dipòsit de la Recerca de Catalunya)
dc.subject.other
Química
cat
dc.title
1,2-Arylsulfonylation of Vinyl Ethers and Esters Enabled by Dual Ni Catalysis
cat
dc.type
info:eu-repo/semantics/article
cat
dc.type
info:eu-repo/semantics/acceptedVersion
cat
dc.relation.projectID
Brazilian funding agencies CNPq (INCT Catálise, Grants No 444061/2018-5 and Universal Project 405052/2021-9)
cat
dc.relation.projectID
FAPESP (21/06099-5, 20/09353-7, 21/ 01354-7, 22/04597-0, 17/10015-6 and 19/ 01560-6 fellowships)
cat
dc.relation.projectID
FEDER/MCI PID2021-123801NB-I00
cat
dc.relation.projectID
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - Brasil (CAPES) - Financial code 001
cat
dc.identifier.doi
https://doi.org/10.1002/cctc.202201434
dc.rights.accessLevel
info:eu-repo/semantics/openAccess
