Abstract
In recent years, the pharmacological potential of quinoxalines has received vast interest due to its many applications. This review centers on a critical overview of chemical diversity and physicochemical properties of bioactive quinoxaline libraries. In addition, recent strategies for obtaining structurally diverse quinoxalines using highly selective processes will be discussed.
Keywords: Quinoxaline, heterocycles, C-H activation, drug-likeness, organometallics.
Current Organic Synthesis
Title:Drug Likeness and Selective Functionalization of Quinoxalines
Volume: 12 Issue: 6
Author(s): Samuel R. A. Ferreira, Marcia S. F. Franco, Evelyn M. L. P. Diniz, Flavio da Silva Emery and Giuliano Cesar Clososki
Affiliation:
Keywords: Quinoxaline, heterocycles, C-H activation, drug-likeness, organometallics.
Abstract: In recent years, the pharmacological potential of quinoxalines has received vast interest due to its many applications. This review centers on a critical overview of chemical diversity and physicochemical properties of bioactive quinoxaline libraries. In addition, recent strategies for obtaining structurally diverse quinoxalines using highly selective processes will be discussed.
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Cite this article as:
Ferreira R. A. Samuel, Franco S. F. Marcia, Diniz M. L. P. Evelyn, Silva Emery da Flavio and Clososki Cesar Giuliano, Drug Likeness and Selective Functionalization of Quinoxalines, Current Organic Synthesis 2015; 12 (6) . https://dx.doi.org/10.2174/157017941206150828110053
DOI https://dx.doi.org/10.2174/157017941206150828110053 |
Print ISSN 1570-1794 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6271 |
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Organic synthesis is a fundamental discipline in chemistry, crucial for the creation of complex molecules with diverse applications in pharmaceuticals, materials science, and beyond. However, the process of designing efficient synthetic routes for target molecules remains challenging. Chemical graph theory, a branch of theoretical chemistry, offers powerful tools for understanding ...read more
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