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2-Amino-5-chloro-1H-pyrrole-3,4-dicarbonitrile

1
Department of Life Sciences, School of Sciences, European University Cyprus, 6 Diogenis Str., Engomi, P.O. Box 22006, 1516 Nicosia, Cyprus
2
Department of Chemistry, University of Cyprus, P.O. Box 20537, 1678 Nicosia, Cyprus
*
Author to whom correspondence should be addressed.
Academic Editor: Luke R. Odell
Molbank 2021, 2021(1), M1191; https://doi.org/10.3390/M1191
Received: 6 February 2021 / Accepted: 11 February 2021 / Published: 13 February 2021
(This article belongs to the Special Issue Heterocycle Reactions)
The reaction of tetracyanoethylene (TCNE) with HCl (g) in the presence of Sn (1 equiv) and AcOH resulted in 2-amino-5-chloro-1H-pyrrole-3,4-dicarbonitrile in a 74% yield. The compound was fully characterized. View Full-Text
Keywords: TCNE; heterocycle; polyfunctionalized; pyrrole; cyano group TCNE; heterocycle; polyfunctionalized; pyrrole; cyano group
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MDPI and ACS Style

Kalogirou, A.S.; Koutentis, P.A. 2-Amino-5-chloro-1H-pyrrole-3,4-dicarbonitrile. Molbank 2021, 2021, M1191. https://doi.org/10.3390/M1191

AMA Style

Kalogirou AS, Koutentis PA. 2-Amino-5-chloro-1H-pyrrole-3,4-dicarbonitrile. Molbank. 2021; 2021(1):M1191. https://doi.org/10.3390/M1191

Chicago/Turabian Style

Kalogirou, Andreas S.; Koutentis, Panayiotis A. 2021. "2-Amino-5-chloro-1H-pyrrole-3,4-dicarbonitrile" Molbank 2021, no. 1: M1191. https://doi.org/10.3390/M1191

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