Issue 1, 2015
From the journal:

Chemical Communications

Isoquinolino[4,3,2-de]phenanthridine: synthesis and its use in 1,3-dipolar cycloadditions to form nitrogen-containing polyaromatic hydrocarbons†

S. Ito,*a   Y. Tokimarua  and  K. Nozaki*a  

* Corresponding authors

a Department of Chemistry and Biotechnology, Graduate School of Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656, Japan
E-mail: ito_shingo@chembio.t.u-tokyo.ac.jp, nozaki@chembio.t.u-tokyo.ac.jp

Abstract

The synthesis of the novel azomethine ylide, isoquinolino[4,3,2-de]phenanthridine, and its use in 1,3-dipolar cycloaddition with various alkenes and alkynes to form the corresponding fused pyrrolidines and pyrroles is reported.

Graphical abstract: Isoquinolino[4,3,2-de]phenanthridine: synthesis and its use in 1,3-dipolar cycloadditions to form nitrogen-containing polyaromatic hydrocarbons

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Article information

DOI
https://doi.org/10.1039/C4CC06643J
Article type
Communication
Submitted
23 Aug 2014
Accepted
03 Nov 2014
First published
04 Nov 2014

Chem. Commun., 2015,51, 221-224

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Isoquinolino[4,3,2-de]phenanthridine: synthesis and its use in 1,3-dipolar cycloadditions to form nitrogen-containing polyaromatic hydrocarbons

S. Ito, Y. Tokimaru and K. Nozaki, Chem. Commun., 2015, 51, 221 DOI: 10.1039/C4CC06643J

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