Visible-Light-Induced Stoichiometric Coupling of Alkylarenes and Trifluoromethyl Ketones
Oxidizing agent
Stoichiometry
Primary (astronomy)
Surface Modification
DOI:
10.1021/acs.orglett.3c01307
Publication Date:
2023-05-17T15:56:51Z
AUTHORS (6)
ABSTRACT
A visible-light induced direct C(sp3)-H functionalization of alkylarenes with trifluoromethyl ketones has been reported to access valuable benzyl-substituted alcohols in a stoichiometric manner. Readily available petroleum-derived are employed as latent benzylation reagents. With bromine radical the hydrogen atom transfer reagent, primary, secondary, and tertiary benzyl C–H bonds suitable coupling partners. Additionally, late-stage modification bioactive molecules highlights potential application this approach.
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