Issue 68, 2019

Synthesis of pyrrolo[3′,2′:4,5][1,3]diazepino[2,1,7-cd]pyrrolizine derivatives from dicyanovinylene-bis(meso-aryl)dipyrrin

Abstract

Pyrrolo[3′,2′:4,5][1,3]diazepino[2,1,7-cd]pyrrolizine derivatives 2 and 3 were synthesized from dicyanovinylene-bis(meso-aryl)dipyrrin in the presence of either BF3·OEt2 or InBr3, where 2 was readily oxidized in aerobic conditions to be 3. It was understood that the fully elongated π-conjugation of 3 is achieved via the conformation of 2. Crystal structures of 2 and 3 were elucidated by X-ray diffraction analysis. Furthermore, two redox states, 3ox and 3red were observed in the chemical redox processes.

Graphical abstract: Synthesis of pyrrolo[3′,2′:4,5][1,3]diazepino[2,1,7-cd]pyrrolizine derivatives from dicyanovinylene-bis(meso-aryl)dipyrrin

Supplementary files

Article information

Article type
Paper
Submitted
28 Oct 2019
Accepted
22 Nov 2019
First published
04 Dec 2019
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2019,9, 40031-40036

Synthesis of pyrrolo[3′,2′:4,5][1,3]diazepino[2,1,7-cd]pyrrolizine derivatives from dicyanovinylene-bis(meso-aryl)dipyrrin

J. Shin, RSC Adv., 2019, 9, 40031 DOI: 10.1039/C9RA08850D

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