2-(2,5-Dimethoxyphenyl)pyrrole-3-carbonitrile-Reference-Cited by-同舟云学术

2-(2,5-Dimethoxyphenyl)pyrrole-3-carbonitrile

Published:2023-04-20 Issue:2 Volume:2023 Page:M1627
ISSN:1422-8599
Container-title:Molbank
language:en
Short-container-title:Molbank

Author:

Grimm Yannic¹,Schollmeyer Dieter¹,Detert Heiner¹

Affiliation:

1. Department of Chemistry, Johannes Gutenberg-Universität Mainz, 55122 Mainz, Germany

Abstract

The Cadogan reaction of 2-aryl-3-nitropyridines leads to δ-carbolines. The title compound is a side product in this reaction, generated via a ring opening of a nitrene and cyclization. A crystal structure analysis gives an enormous unit cell.

Publisher

MDPI AG

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://www.mdpi.com/1422-8599/2023/2/M1627/pdf

Reference23 articles.

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5. Cadogan, J.I.G., and Tait, B.S. (1975). Reduction of nitro- and nitroso-compounds by tervalent phosphorus reagents. Part XV. Reactions of certain aryl 2-nitrophenyl sulphides and their 2-azido-analogues leading to evidence for the intermediacy of 2,3-dihydro-1,3,2-benzothiazaphosph(V)oles (thiazaphosphoranes) and to the formation of dihydrodimethylphenothiazinones and pyrimido- and pyrido-[1,2-b]indazoles. J. Chem. Soc. Perkin Trans. 1, 2396–2405.