Issue 15, 2019

Ring-opening C(sp3)–C coupling of cyclobutanone oxime esters for the preparation of cyanoalkyl containing heterocycles enabled by photocatalysis

Abstract

Here we report a ring-opening C(sp3)–C coupling of cyclobutanone oxime esters for the preparation of cyanoalkyl containing heterocycles under visible-light or sunlight irradiation. The reaction protocol is operationally simple and proceeds at room temperature without extra additives, allowing access to a variety of functionalized alkylnitriles in moderate to excellent yields. This transformation shows wide functional group compatibility and can be easily scaled up. A mechanism study discloses that the cyanoalkyl radical is involved in the present reaction.

Graphical abstract: Ring-opening C(sp3)–C coupling of cyclobutanone oxime esters for the preparation of cyanoalkyl containing heterocycles enabled by photocatalysis

Supplementary files

Article information

Article type
Research Article
Submitted
11 May 2019
Accepted
06 Jun 2019
First published
10 Jun 2019

Org. Chem. Front., 2019,6, 2765-2770

Ring-opening C(sp3)–C coupling of cyclobutanone oxime esters for the preparation of cyanoalkyl containing heterocycles enabled by photocatalysis

W. Zhang, Y. Pan, C. Yang, X. Li and B. Wang, Org. Chem. Front., 2019, 6, 2765 DOI: 10.1039/C9QO00625G

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