Issue 16, 2017

Palladium-catalyzed C–H olefination of uracils and caffeines using molecular oxygen as the sole oxidant

Abstract

The palladium-catalyzed oxidative C–H olefination of uracils or caffeines with alkenes using an atmospheric pressure of molecular oxygen as the sole oxidant has been disclosed. This novel strategy offers an efficient and environmentally friendly method to biologically important C5-alkene uracil derivatives or C8-alkene caffeine derivatives.

Graphical abstract: Palladium-catalyzed C–H olefination of uracils and caffeines using molecular oxygen as the sole oxidant

Supplementary files

Article information

Article type
Paper
Submitted
12 Mar 2017
Accepted
30 Mar 2017
First published
31 Mar 2017

Org. Biomol. Chem., 2017,15, 3499-3506

Palladium-catalyzed C–H olefination of uracils and caffeines using molecular oxygen as the sole oxidant

X. Zhang, L. Su, L. Qiu, Z. Fan, X. Zhang, S. Lin and Q. Huang, Org. Biomol. Chem., 2017, 15, 3499 DOI: 10.1039/C7OB00616K

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