Issue 12, 2016

Iodosobenzene-mediated direct and efficient oxidation of β-dicarbonyls to vicinal tricarbonyls catalyzed by iron(iii) salts

Abstract

Iodosobenzene was found to be effective in the direct oxidation of β-dicarbonyls to vicinal tricarbonyl compounds catalyzed by Fe(NO3)·9H2O under mild and environmentally friendly conditions. Also, the present protocol was applied to the one-pot synthesis of heterocyclic compounds via vicinal tricarbonyls as the reactive intermediates. As for the reaction pathway, a plausible mechanism involving iodonium ylide, reactive carbene species and an α-hydroxylated intermediate was proposed.

Graphical abstract: Iodosobenzene-mediated direct and efficient oxidation of β-dicarbonyls to vicinal tricarbonyls catalyzed by iron(iii) salts

Supplementary files

Article information

Article type
Research Article
Submitted
28 Jul 2016
Accepted
26 Sep 2016
First published
27 Sep 2016

Org. Chem. Front., 2016,3, 1686-1690

Iodosobenzene-mediated direct and efficient oxidation of β-dicarbonyls to vicinal tricarbonyls catalyzed by iron(III) salts

J. Cui, Y. Duan, J. Yu and C. Zhang, Org. Chem. Front., 2016, 3, 1686 DOI: 10.1039/C6QO00405A

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