Methods and Applications of Cycloaddition Reactions in Organic Syntheses

Methods and Applications of Cycloaddition Reactions in Organic Syntheses
Author: Nagatoshi Nishiwaki
Publisher: John Wiley & Sons
Total Pages: 996
Release: 2013-12-17
Genre: Science
ISBN: 1118778200

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Advanced tools for developing new functional materials and applications in chemical research, pharmaceuticals, and materials science Cycloadditions are among the most useful tools for organic chemists, enabling them to build carbocyclic and heterocyclic structures. These structures can then be used to develop a broad range of functional materials, including pharmaceuticals, agrochemicals, dyes, and optics. With contributions from an international team of leading experts and pioneers in cycloaddition chemistry, this book brings together and reviews recent advances, trends, and emerging research in the field. Methods and Applications of Cycloaddition Reactions in Organic Syntheses focuses on two component cycloadditions, with chapters covering such topics as: N1 unit transfer reaction to C–C double bonds [3+2] Cycloaddition of α, β-unsaturated metal-carbene complexes Formal [3+3] cycloaddition approach to natural product synthesis Development of new methods for the construction of heterocycles based on cycloaddition reaction of 1,3-dipoles Cycloreversion approach for preparation of large π-conjugated compounds Transition metal-catalyzed or mediated [5+1] cycloadditions Readers will learn methods for seamlessly executing important reactions such as Diels-Alder and stereoselective dipolar reactions in order to fabricate heterocyclic compounds, natural products, and functional molecules. The book not only features cutting-edge topics, but also important background information, such as the contributors’ process for developing new methodologies, to help novices become fully adept in the field. References at the end of each chapter lead to original research papers and reviews for facilitating further investigation of individual topics. Covering the state of the science and technology, Methods and Applications of Cycloaddition Reactions in Organic Syntheses enables synthetic organic chemists to advance their research and develop new functional materials and applications in chemical research, pharmaceuticals, and materials science.


Methods and Applications of Cycloaddition Reactions in Organic Syntheses
Language: en
Pages: 996
Authors: Nagatoshi Nishiwaki
Categories: Science
Type: BOOK - Published: 2013-12-17 - Publisher: John Wiley & Sons

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Advanced tools for developing new functional materials and applications in chemical research, pharmaceuticals, and materials science Cycloadditions are among th
Cycloaddition Reactions in Organic Synthesis
Language: en
Pages: 354
Authors: Shu Kobayashi
Categories: Science
Type: BOOK - Published: 2002 - Publisher: John Wiley & Sons

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During the miners' strike in the 1980s, a worker is killed in the striking coalfields of Wales. Some months later, a government minister thought to be connected
Cycloaddition Reactions in Organic Synthesis
Language: en
Pages: 388
Authors: W. Carruthers
Categories: Science
Type: BOOK - Published: 1990 - Publisher: Elsevier Science & Technology

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Paperback. Demonstrates the wide scope of cycloaddition reactions, including the Diels-Alder reaction, the ene reaction, 1,3-dipolar cycloadditions and [2]2] cy
Synthetic Applications of 1,3-Dipolar Cycloaddition Chemistry Toward Heterocycles and Natural Products, Volume 59
Language: en
Pages: 952
Authors: Albert Padwa
Categories: Science
Type: BOOK - Published: 2003-04-14 - Publisher: John Wiley & Sons

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Dipolar cycloaddition reactions have found many useful applications in chemistry, particularly with respect to the synthesis of compounds with new chiral center
The Diels-Alder Reaction
Language: en
Pages: 364
Authors: Francesco Fringuelli
Categories: Science
Type: BOOK - Published: 2002-01-21 - Publisher: John Wiley & Sons

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70 Jahre Forschung an der Diels-Alder-Reaktion: Dieses Buch fasst die wichtigsten und beeindruckendsten Ergebnisse in einzigartiger Weise zusammen! Zunächst we