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Quinoxalines = Synthesis, Reactions,...
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Quinoxalines = Synthesis, Reactions, Mechanisms and Structure /
Record Type:
Language materials, printed : Monograph/item
Title/Author:
Quinoxalines/ by Vakhid A. Mamedov.
Reminder of title:
Synthesis, Reactions, Mechanisms and Structure /
Author:
Mamedov, Vakhid A.
Description:
XV, 437 p. 591 illus., 546 illus. in color.online resource. :
Contained By:
Springer Nature eBook
Subject:
Organic chemistry. -
Online resource:
https://doi.org/10.1007/978-3-319-29773-6
ISBN:
9783319297736
Quinoxalines = Synthesis, Reactions, Mechanisms and Structure /
Mamedov, Vakhid A.
Quinoxalines
Synthesis, Reactions, Mechanisms and Structure /[electronic resource] :by Vakhid A. Mamedov. - 1st ed. 2016. - XV, 437 p. 591 illus., 546 illus. in color.online resource.
Introduction: Quinoxaline as a Parent Heterocycle -- Synthesis of Quinoxalines -- Synthesis of Pyrrolo[l,2-a]quinoxalines -- Synthesis of Imidazo[1,5-a]- and Imidazo[1,2-a]quinoxalines -- Synthesis of Quinoxaline Macrocycles -- Rearrangements of Quinoxalin(on)es in the Synthesis of Benzimidazol(on)es -- Appendix.
This book reviews the fundamental aspects of quinoxaline chemistry: synthesis, reactions, mechanisms, structure, properties, and uses. The first four chapters present a survey of the developments in quinoxaline chemistry since the publication of the monograph on “Condensed Pyrazines” by Cheeseman and Cookson in 1979. These chapters give comprehensive coverage of all the methods of the synthesis of quinoxalines and the important quinoxaline-containing ring systems such as thiazolo[3,4-a]-, pyrrolo[1,2-a]-, and imidazo[1,5-a]quinoxalines. Chapter five describes many new methods for the construction of quinoxaline macrocycles, which are important in applications such as optical devices and materials. The final chapter reviews all previously known rearrangements of heterocyclic systems that lead to benzimidazole derivatives. Mamedov critically analyses these transformations to reveal a novel acid-catalyzed rearrangement of quinoxalinones giving 2-heteroarylbenzimidazoles and 1-heteroarylbenzimidazolones in the presence of nucleophilic reactants (MAMEDOV Heterocycle Rearrangement). This book is of interest to researchers in the fields of heterocyclic and synthetic organic chemistry. .
ISBN: 9783319297736
Standard No.: 10.1007/978-3-319-29773-6doiSubjects--Topical Terms:
1148722
Organic chemistry.
LC Class. No.: QD415-436
Dewey Class. No.: 547
Quinoxalines = Synthesis, Reactions, Mechanisms and Structure /
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Introduction: Quinoxaline as a Parent Heterocycle -- Synthesis of Quinoxalines -- Synthesis of Pyrrolo[l,2-a]quinoxalines -- Synthesis of Imidazo[1,5-a]- and Imidazo[1,2-a]quinoxalines -- Synthesis of Quinoxaline Macrocycles -- Rearrangements of Quinoxalin(on)es in the Synthesis of Benzimidazol(on)es -- Appendix.
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This book reviews the fundamental aspects of quinoxaline chemistry: synthesis, reactions, mechanisms, structure, properties, and uses. The first four chapters present a survey of the developments in quinoxaline chemistry since the publication of the monograph on “Condensed Pyrazines” by Cheeseman and Cookson in 1979. These chapters give comprehensive coverage of all the methods of the synthesis of quinoxalines and the important quinoxaline-containing ring systems such as thiazolo[3,4-a]-, pyrrolo[1,2-a]-, and imidazo[1,5-a]quinoxalines. Chapter five describes many new methods for the construction of quinoxaline macrocycles, which are important in applications such as optical devices and materials. The final chapter reviews all previously known rearrangements of heterocyclic systems that lead to benzimidazole derivatives. Mamedov critically analyses these transformations to reveal a novel acid-catalyzed rearrangement of quinoxalinones giving 2-heteroarylbenzimidazoles and 1-heteroarylbenzimidazolones in the presence of nucleophilic reactants (MAMEDOV Heterocycle Rearrangement). This book is of interest to researchers in the fields of heterocyclic and synthetic organic chemistry. .
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