Synthesis of multi-substituted pyridines from ylidenemalononitriles and their emission properties-Reference-Cited by-同舟云学术

Synthesis of multi-substituted pyridines from ylidenemalononitriles and their emission properties

Published:2021 Issue:9 Volume:19 Page:1991-1999
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

de Souza Juliana M.¹²³⁴⁵,Abdiaj Irini¹²³⁴,Chen Jiaqi⁶⁷⁸⁴,Hanson Kenneth⁶⁷⁸⁴^ORCID,de Oliveira Kleber T.⁵⁹¹⁰¹¹^ORCID,McQuade D. Tyler¹²³⁴

Affiliation:

1. Department of Chemical and Life Science Engineering

2. Virginia Commonwealth University

3. Richmond

4. USA

5. Departamento de Química

6. Department of Chemistry & Biochemistry

7. Florida State University

8. Tallahassee

9. Universidade Federal de São Carlos

10. São Carlos

11. Brazil

Abstract

A mild and solvent-free methodology to obtain a scope of multi-substituted pyridines at room temperature is presented. One of the resulting amino-nicotinonitriles exhibits a preliminary evidence of aggregation-induced emission (AIE).

Funder

National Institutes of Health

Fundação de Amparo à Pesquisa do Estado de São Paulo

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/OB/D0OB02591G

Reference44 articles.

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2. F. Yates , R. T.Courts and A. F.Casy , in Pyridine and Its Derivatives; supplement IV , ed. R. A. Abramovitch , Wiley , New York , 1975 , p. 445

3. E. F. V. Scriven , Pyridines: from Lab to Production , Elsevier , Amsterdam , 1st edn, 2013

4. Investigating the continuous synthesis of a nicotinonitrile precursor to nevirapine

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