Issue 29, 2024

Trifunctionalization of C[double bond, length as m-dash]C bonds in vinyl azides to access densely functionalized phenanthridines enabled by the NCS/AgNO2 system

Abstract

An unprecedented trifunctionalization of C[double bond, length as m-dash]C bonds in 2-(1-azidovinyl)-1,1′-biphenyls has been successfully achieved using the NCS/AgNO2 system, leading to the preparation of 6-(dichloro(nitro)methyl)phenanthridines in moderate to good yields. In this process, the NCS/AgNO2 system serves as a NO2 radical initiator as well as a chloro group source. The present protocol is a rare example of the selective construction of densely functionalized phenanthridine derivatives in a one-pot manner.

Graphical abstract: Trifunctionalization of C [[double bond, length as m-dash]] C bonds in vinyl azides to access densely functionalized phenanthridines enabled by the NCS/AgNO2 system

Supplementary files

Article information

Article type
Paper
Submitted
30 May 2024
Accepted
02 Jul 2024
First published
03 Jul 2024

Org. Biomol. Chem., 2024,22, 5982-5986

Trifunctionalization of C[double bond, length as m-dash]C bonds in vinyl azides to access densely functionalized phenanthridines enabled by the NCS/AgNO2 system

S. Ren, J. Zhu and Y. Liu, Org. Biomol. Chem., 2024, 22, 5982 DOI: 10.1039/D4OB00905C

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