Issue 91, 2016

Iron-catalyzed oxidative sp3 carbon–hydrogen bond functionalization of 3,4-dihydro-1,4-benzoxazin-2-ones

Abstract

A novel and efficient iron-catalyzed sp3 carbon–hydrogen bond functionalization of benzoxazinone derivatives has been developed. For the first time, benzoxazin-2-ones were used as substrates in an oxidative dehydrogenative coupling reaction. The experiments were performed under mild reaction conditions to construct alkyl–aryl C(sp3)–C(sp2) bonds. The application of this method to the gram-scale synthesis of natural product cephalandole A has been accomplished in a 3-step sequence. A plausible one electron oxidation involved mechanism is proposed.

Graphical abstract: Iron-catalyzed oxidative sp3 carbon–hydrogen bond functionalization of 3,4-dihydro-1,4-benzoxazin-2-ones

Supplementary files

Article information

Article type
Communication
Submitted
17 Jul 2016
Accepted
08 Sep 2016
First published
09 Sep 2016

Chem. Commun., 2016,52, 13341-13344

Iron-catalyzed oxidative sp3 carbon–hydrogen bond functionalization of 3,4-dihydro-1,4-benzoxazin-2-ones

C. Huo, J. Dong, Y. Su, J. Tang and F. Chen, Chem. Commun., 2016, 52, 13341 DOI: 10.1039/C6CC05885J

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