Sulfur-Arylation of Sulfenamides via Ullmann-Type Coupling with (Hetero)aryl Iodides.
Journal
Organic letters
ISSN: 1523-7052
Titre abrégé: Org Lett
Pays: United States
ID NLM: 100890393
Informations de publication
Date de publication:
30 Jun 2023
30 Jun 2023
Historique:
pmc-release:
30
06
2024
medline:
3
7
2023
pubmed:
20
6
2023
entrez:
20
6
2023
Statut:
ppublish
Résumé
Sulfur-(hetero)arylation of sulfenamides with commercially abundant (hetero)aryl iodides by Ullmann-type coupling with inexpensive copper(I) iodide as the catalyst is reported. A broad scope of reaction inputs was demonstrated, including both aryl and alkyl sulfenamides and highly sterically hindered aryl and 5- and 6-membered ring heteroaryl iodides. Relevant to many bioactive high oxidation state sulfur compounds, the (hetero)arylation of
Identifiants
pubmed: 37338140
doi: 10.1021/acs.orglett.3c01874
pmc: PMC10330900
mid: NIHMS1913721
doi:
Substances chimiques
Iodides
0
sulfenamide
0
Sulfamerazine
UR1SAB295F
Sulfur
70FD1KFU70
Sulfur Compounds
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
4759-4764Subventions
Organisme : NIGMS NIH HHS
ID : R35 GM122473
Pays : United States
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