Metal-free nucleophilic trifluoromethylselenolation via an iodide-mediated umpolung reactivity of trifluoromethylselenotoluenesulfonate.
fluorine
nucleophilic substitution
perfluoroalkylselenolation
selenium
trifluoromethylselenolation
Journal
Beilstein journal of organic chemistry
ISSN: 1860-5397
Titre abrégé: Beilstein J Org Chem
Pays: Germany
ID NLM: 101250746
Informations de publication
Date de publication:
2020
2020
Historique:
received:
23
10
2020
accepted:
02
12
2020
entrez:
28
12
2020
pubmed:
29
12
2020
medline:
29
12
2020
Statut:
epublish
Résumé
We report herein a practical method to generate CF
Identifiants
pubmed: 33363671
doi: 10.3762/bjoc.16.252
pmc: PMC7736694
doi:
Types de publication
Journal Article
Langues
eng
Pagination
3032-3037Informations de copyright
Copyright © 2020, Grollier et al.; licensee Beilstein-Institut.
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