Issue 39, 2021

Iron-catalyzed radical cascade cyclization of oxime esters with isocyanides: synthesis of 1-cyanoalkyl isoquinolines and 6-cyanoalkyl phenanthridines

Abstract

An iron-catalyzed radical cascade cyclization of oxime esters with isocyanides for the synthesis of 1-cyanoalkyl isoquinolines and 6-cyanoalkyl phenanthridines has been developed. This demonstrates excellent functional group tolerance and broad substrate scope. A diverse range of potentially valuable 1-cyanoalkyl isoquinolines and 6-cyanoalkyl phenanthridines were obtained in moderate to good yields.

Graphical abstract: Iron-catalyzed radical cascade cyclization of oxime esters with isocyanides: synthesis of 1-cyanoalkyl isoquinolines and 6-cyanoalkyl phenanthridines

Supplementary files

Article information

Article type
Paper
Submitted
08 Aug 2021
Accepted
16 Sep 2021
First published
16 Sep 2021

Org. Biomol. Chem., 2021,19, 8597-8606

Iron-catalyzed radical cascade cyclization of oxime esters with isocyanides: synthesis of 1-cyanoalkyl isoquinolines and 6-cyanoalkyl phenanthridines

D. Xue, R. Liu, D. Zhang, N. Li, Y. Xue, Q. Ge and L. Shao, Org. Biomol. Chem., 2021, 19, 8597 DOI: 10.1039/D1OB01556G

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