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Synthetic Applications of 1,3-Dipolar Cycloaddition Chemistry Toward Heterocycles and Natural Products, Albert Padwa


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Автор: Albert Padwa
Название:  Synthetic Applications of 1,3-Dipolar Cycloaddition Chemistry Toward Heterocycles and Natural Products
Перевод названия: Синтетические приложения 1,3-диполярного циклоприсоединения к гетероциклам
ISBN: 9780471387268
Издательство: Wiley
Классификация:


ISBN-10: 0471387266
Обложка/Формат: Hardcover
Страницы: 952
Вес: 1.30 кг.
Дата издания: May 16, 2002
Язык: English
Ссылка на Издательство: Link
Поставляется из: Англии
Описание: A comprehensive reference on the synthetic chemistry of cycloaddition reactions Dipolar cycloaddion reactions have found many useful applications in chemistry, particularly with respect to the synthesis of compounds with new chiral centers. Such asymmetric syntheses have a growing importance in the pharmaceutical and agricultural industries with respect to the preparation of chiral drugs and natural products. This much-needed volume updates the popular 1984 edition with advances made over the last twenty years in cycloaddition reactions. While the 1984 volume focused on theory, structure, reactivities, and selectivities, the new volume is geared toward synthetic applications. Both carbonyl ylides and nitronates, important members of the 1,3-dipole family that were not reviewed previously, are now included. Also, beyond the capability of the 1,3-dipolar cycloadditon reaction to produce heterocycles, the ability of heteroatom-containing cycloadducts to transform into a variety of other functionalized organic molecules, cylclic or acyclic, and the ability of many 1,3-dipolar cycloadditions to generate rings containing several contiguous stereocenters in one synthetic operation is discussed. Volume 59 provides the only comprehensive reference on the market detailing the synthetic chemistry of cycloaddition reactions.
Дополнительное описание: Кол-во стр.: 952
Формат: 241 x 164
Дата издания: 2002
Илюстрации: Illustrations
Вес: 1304
Круг читателей: undergraduate; postgraduate; research, professional




The Chemistry of Heterocycles

Автор: Ji Ram, Vishnu
Название: The Chemistry of Heterocycles
ISBN: 0081010338 ISBN-13(EAN): 9780081010334
Издательство: Elsevier Science
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Цена: 26107.00 р.
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Описание:

Heterocycles are ubiquitously present in nature and occupy a unique place in organic chemistry as they are part of the DNA and haemoglobin that make the life possible.

The Chemistry of Heterocycles Volume 1 covers an introduction to the topic, followed by a chapter on the nomenclature of all classes of isolated, fused and polycyclic heterocycles. The third chapter delineates the highly strained three membered N, O and S containing aromatic and non-aromatic heterocycles with one and more than one similar and dissimilar heteroatom. The four-membered heterocycles are abundantly present in various natural and synthetic products of pharmacological importance. This chapter describes the natural abundance, synthesis, chemical reactivity, structural features and their medicinal importance. This class of compounds are present as sub-structures in penicillin and cytotoxic Taxol. Lastly, a chapter on the natural abundance, synthesis, chemical reactivity and pharmacological importance of 5-membered heterocycles with N, O, S heteroatom is covered. The chemistry of heterocycles with mixed heteroatom such as, N-S, N-O, N-S etc. is also described.

  • Gives in-depth, clear information about various systems of nomenclature along with widely acceptable IUPAC system for naming various classes of heterocycles
  • Provides complete information about natural occurrences, synthesis, chemical reactivity, pharmacological importance of heterocycles and their application in material science
  • Highly relevant for graduate students and researchers, providing updated information about various isolated and fused N, O and, S containing heterocycles
Incorporation of Heterocycles into Combinatorial Chemistry

Автор: Babaev
Название: Incorporation of Heterocycles into Combinatorial Chemistry
ISBN: 3319500139 ISBN-13(EAN): 9783319500133
Издательство: Springer
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Цена: 7685.00 р.
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Описание: The author has summarized a decade of teaching combinatorial chemistry into this timely brief. The solid phase synthesis of unnatural heterocyclic alpha-amino acids is illustrated by practical examples starting from the ABCs of peptide synthesis explored in chapter one. Chapter two is concerned with the solid phase synthesis which is shown on various techniques – BillBoard, tea-bag, and Lantern devices, and demonstrated on heterocyclic examples and protocols. In the third chapter the tools for accelerating chemical synthesis – solid phase and liquid phase – are reviewed. Here the techniques of parallel refluxing (including microwave and flow technique) and parallel separation (filtration, centrifugation, evaporation, and chromatography) are described. In the chapters 4 and 5 the author goes on to describe how the liquid phase synthesis of heterocycles (reductive amination and Ugi reaction of heterocycles) is illustrated with the use of semi-automated protocols. Finally, the design of combinatorial libraries of heterocycles is reviewed including the original author’s findings.

Synthesis of Heterocycles in Contemporary Medicinal Chemistry

Автор: ?asar
Название: Synthesis of Heterocycles in Contemporary Medicinal Chemistry
ISBN: 3319399152 ISBN-13(EAN): 9783319399157
Издательство: Springer
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Цена: 36570.00 р.
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Описание: The series Topics in Heterocyclic Chemistry presents critical reviews on present and future trends in the research of heterocyclic compounds. Overall the scope is to cover topics dealing with all areas within heterocyclic chemistry, both experimental and theoretical, of interest to the general heterocyclic chemistry community. The series consists of topic related volumes edited by renowned editors with contributions of experts in the field. All chapters from Topics in Heterocyclic Chemistry are published Online First with an individual DOI. In references, Topics in Heterocyclic Chemistry is abbreviated as Top Heterocycl Chem and cited as a journal.


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