Issue 93, 2015
From the journal:

RSC Advances

Light triggered addition/annulation of 2-isocyanobiphenyls toward 6-trifluoromethyl-phenanthridines under photocatalyst-free conditions†

Xiangyang Tang,a   Shuang Song,a   Cuibo Liu,*ab   Rongjiao Zhua  and  Bin Zhang*abc  

* Corresponding authors

a Department of Chemistry, School of Science, Tianjin University, Tianjin 300072, China
E-mail: bzhang@tju.edu.cn, chemliucuibo@163.com

b Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin 300072, China

c The Key Lab of Systems Bioengineering, Ministry of Education, Tianjin University, Tianjin 300072, China

Abstract

A photocatalyst-free, light promoted sequential radical addition/annulation of 2-isocyanobiphenyls to 6-trifluoromethyl phenanthridines is presented. Wide substrate scopes and scale-up experiment demonstrate the promising efficiency and utility of this strategy.

Graphical abstract: Light triggered addition/annulation of 2-isocyanobiphenyls toward 6-trifluoromethyl-phenanthridines under photocatalyst-free conditions

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Article information

DOI
https://doi.org/10.1039/C5RA16645D
Article type
Communication
Submitted
18 Aug 2015
Accepted
03 Sep 2015
First published
04 Sep 2015

RSC Adv., 2015,5, 76363-76367

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Light triggered addition/annulation of 2-isocyanobiphenyls toward 6-trifluoromethyl-phenanthridines under photocatalyst-free conditions

X. Tang, S. Song, C. Liu, R. Zhu and B. Zhang, RSC Adv., 2015, 5, 76363 DOI: 10.1039/C5RA16645D

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