Synthesis of <i>N</i>-arylsulfonamides via Chan-Lam Coupling Between Aryl Boronic Acids and <i>N</i>-[(sulfonyl)imino]phenyliodinanes
dc.contributor.author | Merchan-Arenas, Diego R. | |
dc.contributor.author | Rivero-Jerez, Paula S. | |
dc.contributor.author | Perez, Edwin G. | |
dc.date.accessioned | 2025-01-20T22:04:15Z | |
dc.date.available | 2025-01-20T22:04:15Z | |
dc.date.issued | 2021 | |
dc.description.abstract | We synthesized a library of 32 sulfonamides via CuBr2 catalyzed Chan-Lam C-N coupling, reaching excellent yields (until 81 %) under ligand-base-free, mild conditions, and short reaction times. A new non-toxic, versatile and easy to prepare starting materials, N-[(Sulfonyl)imino]phenyliodinanes were first time proposed as the nitrogen source in this synthetic tool. Finally, the sulfonamides were used as valuable building blocks in the synthesis of mono-alkyl anilines through their alkylation and Fukuyama deprotection steps. | |
dc.fuente.origen | WOS | |
dc.identifier.doi | 10.1002/slct.202103876 | |
dc.identifier.issn | 2365-6549 | |
dc.identifier.uri | https://doi.org/10.1002/slct.202103876 | |
dc.identifier.uri | https://repositorio.uc.cl/handle/11534/94074 | |
dc.identifier.wosid | WOS:000726827000026 | |
dc.issue.numero | 45 | |
dc.language.iso | en | |
dc.pagina.final | 12810 | |
dc.pagina.inicio | 12806 | |
dc.revista | Chemistryselect | |
dc.rights | acceso restringido | |
dc.subject | Chan-Lam C-N coupling | |
dc.subject | Iodinanes | |
dc.subject | N-aryl sulfonamides | |
dc.subject | monoalkyl anilines | |
dc.title | Synthesis of <i>N</i>-arylsulfonamides via Chan-Lam Coupling Between Aryl Boronic Acids and <i>N</i>-[(sulfonyl)imino]phenyliodinanes | |
dc.type | artículo | |
dc.volumen | 6 | |
sipa.index | WOS | |
sipa.trazabilidad | WOS;2025-01-12 |