Vakhid a mamedov quinoxalines synthesis, reactions, mechanisms and structure springer (2016)
➤ Gửi thông báo lỗi ⚠️ Báo cáo tài liệu vi phạmNội dung chi tiết: Vakhid a mamedov quinoxalines synthesis, reactions, mechanisms and structure springer (2016)
Vakhid a mamedov quinoxalines synthesis, reactions, mechanisms and structure springer (2016)
Vakhid A. MamedovQuinoxalinesSynthesis, Reactions, Mechanisms and StructureVakhid A. MamedovQuinoxalinesSynthesis, Reactions, Mechanisms and Structure Vakhid a mamedov quinoxalines synthesis, reactions, mechanisms and structure springer (2016) eSpringerVakhid A. MamedovA.E. Arbuzov Institute of Organic andPhysical ChemistryKazan Scientific Center. Russian Academy of SciencesKazanRussiaISBN 978-3-319-29771-2 ISBN 978-3-319-29773-6 (eBook)DOI 10.1007/978-3-319-29773-6Library of Congress Control Number: 2016931837•V) Springer International P Vakhid a mamedov quinoxalines synthesis, reactions, mechanisms and structure springer (2016) ublishing Switzerland 2016This work is subject to copyright. All rights are reserved by the Publisher, whether the whole or part of the material is coVakhid a mamedov quinoxalines synthesis, reactions, mechanisms and structure springer (2016)
ncerned, specifically the rights of translation, reprinting, reuse of illustrations, recitation, broadcasting, reproduction on microfilms or in any otVakhid A. MamedovQuinoxalinesSynthesis, Reactions, Mechanisms and StructureVakhid A. MamedovQuinoxalinesSynthesis, Reactions, Mechanisms and Structure Vakhid a mamedov quinoxalines synthesis, reactions, mechanisms and structure springer (2016) logy now known or hereafter developed.The use of general descriptive names, registered names, trademarks, service marks, etc. in this publication does not imply, even in the absence of a specific statement, that such names are exempt from the relevant protective laws and regulations and therefore fr Vakhid a mamedov quinoxalines synthesis, reactions, mechanisms and structure springer (2016) ee for general use.The publisher, the authors and the editors arc safe to assume that the advice and information in this IxMlk arc believed to be trueVakhid a mamedov quinoxalines synthesis, reactions, mechanisms and structure springer (2016)
and accurate at the date of publication. Neither the publisher nor the authors or the editors give a warranty, express or implied, with respect to thVakhid A. MamedovQuinoxalinesSynthesis, Reactions, Mechanisms and StructureVakhid A. MamedovQuinoxalinesSynthesis, Reactions, Mechanisms and Structure Vakhid a mamedov quinoxalines synthesis, reactions, mechanisms and structure springer (2016) ingerNatureThe registered company is springer International Publishing AG SwitzerlandForewordHeterocycles form a fundamental basis for the development of pharmaceutical and agricultural products with wide applications. In this book the author describes the synthesis, and the chemical properties of a Vakhid a mamedov quinoxalines synthesis, reactions, mechanisms and structure springer (2016) n important class of heterocyclic chemistry, the quinoxalines.Chapter 1describes some properties of the Quinoxaline-As a Parent Heterocycle.Chapter 2cVakhid a mamedov quinoxalines synthesis, reactions, mechanisms and structure springer (2016)
overs recent advances in the Synthesis of Quinoxalines involving the methods based on the (a) condensation of 1,2-diaminobenzcncs and derivatives withVakhid A. MamedovQuinoxalinesSynthesis, Reactions, Mechanisms and StructureVakhid A. MamedovQuinoxalinesSynthesis, Reactions, Mechanisms and Structure Vakhid a mamedov quinoxalines synthesis, reactions, mechanisms and structure springer (2016) of MA'-dimethyl(dibenzyf)ethylencdiamine with 1,2- and 1,4-dihydroxybenzenes. (d) synthesis of quinoxalines from aniline and its derivatives, (c) synthesis of quinoxalines from heterocyclic systems and (f) synthesis of quinoxalines based on the carbocyclic system.From the data presented in this chap Vakhid a mamedov quinoxalines synthesis, reactions, mechanisms and structure springer (2016) ter many original and interesting methods recently appeared for the synthesis of quinoxalines, which arc difficult to obtain or in general arc unobtaiVakhid a mamedov quinoxalines synthesis, reactions, mechanisms and structure springer (2016)
nable. These new methods by Kaufmann. Tanimori, Kalinski and Shaabani are based on the reactions of a wide variety of compounds that deserve further aVakhid A. MamedovQuinoxalinesSynthesis, Reactions, Mechanisms and StructureVakhid A. MamedovQuinoxalinesSynthesis, Reactions, Mechanisms and Structure Vakhid a mamedov quinoxalines synthesis, reactions, mechanisms and structure springer (2016) Synthesis of hnidazol l.5-«|- and Imidazol l,2-tf|quinoxalincs. Chapter 5 discusses the Synthesis of Quinoxaline Macrocycles through (a) introduction of the quinoxaline system into macrocycles, (b) the closing of l.n-bis(quinoxalin-l-yl)alkancs and (c) from both resorcin |4|arenes and quinoxalines. Vakhid a mamedov quinoxalines synthesis, reactions, mechanisms and structure springer (2016) Chapter 6 demonstrates all known Rearrangements of Quinoxalin(on)cs in the Synthesis of Bcnzimidazol(on)es and the interesting new rearrangements disVakhid a mamedov quinoxalines synthesis, reactions, mechanisms and structure springer (2016)
covered by Mamedov, the author of this book, comprising (a) the acid catalysed conversion of “any of the spiro-derivatives of l,2,3,4-tetrahydrtinquinVakhid A. MamedovQuinoxalinesSynthesis, Reactions, Mechanisms and StructureVakhid A. MamedovQuinoxalinesSynthesis, Reactions, Mechanisms and StructureVakhid A. MamedovQuinoxalinesSynthesis, Reactions, Mechanisms and StructureVakhid A. MamedovQuinoxalinesSynthesis, Reactions, Mechanisms and StructureGọi ngay
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