Issue 4, 2017

Convenient synthesis of 6-alkyl phenanthridines and 1-alkyl isoquinolines via silver-catalyzed oxidative radical decarboxylation

Abstract

A convenient and efficient protocol for the synthesis of 6-alkyl phenanthridines and 1-alkyl isoquinolines has been developed. The reaction relies on the coupling of 2-isocyanobiphenyls and vinyl isonitriles with alkyl radicals formed by the silver-catalyzed decarboxylation of stoichiometric aliphatic carboxylic acids, and affords diverse phenanthridine and isoquinoline derivatives under mild reaction conditions. The experiment of β-scission of cyclobutylcarbinyl radicals is used to shed light on the reaction mechanism.

Graphical abstract: Convenient synthesis of 6-alkyl phenanthridines and 1-alkyl isoquinolines via silver-catalyzed oxidative radical decarboxylation

Supplementary files

Article information

Article type
Paper
Submitted
26 Oct 2016
Accepted
23 Dec 2016
First published
23 Dec 2016

Org. Biomol. Chem., 2017,15, 957-971

Convenient synthesis of 6-alkyl phenanthridines and 1-alkyl isoquinolines via silver-catalyzed oxidative radical decarboxylation

Q. Yao, X. Zhou, X. Zhang, C. Wang, P. Wang and M. Li, Org. Biomol. Chem., 2017, 15, 957 DOI: 10.1039/C6OB02331B

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