Deoxytrifluoromethylation of Alcohols.


Journal

Journal of the American Chemical Society
ISSN: 1520-5126
Titre abrégé: J Am Chem Soc
Pays: United States
ID NLM: 7503056

Informations de publication

Date de publication:
13 07 2022
Historique:
pubmed: 6 7 2022
medline: 15 7 2022
entrez: 5 7 2022
Statut: ppublish

Résumé

Deoxy-functionalization of alcohols represents a class of reactions that has had a profound impact on modern medicine. In particular, deoxyfluorination is commonly employed as a means to incorporate high-value fluorine atoms into drug-like molecules. Recently, the trifluoromethyl (CF

Identifiants

pubmed: 35786873
doi: 10.1021/jacs.2c04807
pmc: PMC9676087
mid: NIHMS1850482
doi:

Substances chimiques

Alcohols 0
Hydrocarbons, Fluorinated 0
Copper 789U1901C5

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

11961-11968

Subventions

Organisme : NIGMS NIH HHS
ID : R35 GM134897
Pays : United States

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Auteurs

Nicholas E Intermaggio (NE)

Merck Center for Catalysis at Princeton University, Princeton, New Jersey 08544, United States.

Agustin Millet (A)

Merck Center for Catalysis at Princeton University, Princeton, New Jersey 08544, United States.

Dali L Davis (DL)

Merck Center for Catalysis at Princeton University, Princeton, New Jersey 08544, United States.

David W C MacMillan (DWC)

Merck Center for Catalysis at Princeton University, Princeton, New Jersey 08544, United States.

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Classifications MeSH