Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2018 Apr 3;57(15):4078-4082.
doi: 10.1002/anie.201800818. Epub 2018 Mar 12.

Selective C(sp3 )-H Aerobic Oxidation Enabled by Decatungstate Photocatalysis in Flow

Affiliations

Selective C(sp3 )-H Aerobic Oxidation Enabled by Decatungstate Photocatalysis in Flow

Gabriele Laudadio et al. Angew Chem Int Ed Engl. .

Abstract

A mild and selective C(sp3 )-H aerobic oxidation enabled by decatungstate photocatalysis has been developed. The reaction can be significantly improved in a microflow reactor enabling the safe use of oxygen and enhanced irradiation of the reaction mixture. Our method allows for the oxidation of both activated and unactivated C-H bonds (30 examples). The ability to selectively oxidize natural scaffolds, such as (-)-ambroxide, pregnenolone acetate, (+)-sclareolide, and artemisinin, exemplifies the utility of this new method.

Keywords: C(sp3)−H functionalization; aerobic oxidation; decatungstate; flow chemistry; photocatalysis.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Scheme 1
Scheme 1
a) Transition‐metal‐catalyzed C(sp3)−H oxidation strategies. b) Electrochemical C(sp3)−H oxidation. c) Our strategy for selective C(sp3)−H aerobic oxidation enabled by decatungstate photocatalysis in flow.
Scheme 2
Scheme 2
Scope of the C(sp3)−H oxidation enabled by decatungstate photocatalysis in flow. The oxidation site is indicated in gray and with an asterisk, unless otherwise noted. [a] The yield was determined by GC. [b] The reaction was carried out in the absence of 1 m HCl. [c] The reaction was carried out with CH3CN/dichloromethane (2.5:1) as the solvent. [d] The reaction was carried out with a residence time of 1.5 h. Boc=tert‐butoxycarbonyl.

Similar articles

Cited by

References

    1. None
    1. He J., Wasa M., Chan K. S. L., Shao Q., Yu J. Q., Chem. Rev. 2017, 117, 8754–8786; - PMC - PubMed
    1. Roudesly F., Oble J., Poli G., J. Mol. Catal. A 2017, 426, 275–296;
    1. Gensch T., Hopkinson M. N., Glorius F., Wencel-Delord J., Chem. Soc. Rev. 2016, 45, 2900–2936; - PubMed
    1. Hartwig J. F., J. Am. Chem. Soc. 2016, 138, 2–24; - PMC - PubMed

Publication types