Organic Azides

Organic Azides

Author: Stefan Bräse

Publisher: John Wiley & Sons

Published: 2011-09-23

Total Pages: 536

ISBN-13: 0470682523

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Most current state-of-the-art overview of this important class of compounds, encompassing many new and emerging applications The number of articles on organic azides continues to increase tremendously; on average, there are more than 1000 new publications a year Covers basic chemistry as well as state-of-the-art applications in life science and materials science World-ranked authors describe their own research in the wider context of azide chemistry Includes a chapter on safe synthesis and handling (azides can decompose explosively)


Organic Azides

Organic Azides

Author: Stefan Bräse

Publisher: John Wiley & Sons

Published: 2010-02-01

Total Pages: 537

ISBN-13: 0470519983

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Most current state-of-the-art overview of this important class of compounds, encompassing many new and emerging applications The number of articles on organic azides continues to increase tremendously; on average, there are more than 1000 new publications a year Covers basic chemistry as well as state-of-the-art applications in life science and materials science World-ranked authors describe their own research in the wider context of azide chemistry Includes a chapter on safe synthesis and handling (azides can decompose explosively)


Azides and Nitrenes

Azides and Nitrenes

Author: Eric Scriven

Publisher: Elsevier

Published: 2012-12-02

Total Pages: 557

ISBN-13: 0323146236

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Azides and Nitrenes: Reactivity and Utility provides information pertinent to the fundamentals aspects of the chemistry of azides and nitrenes. This book discusses the mechanism and synthetic applications of alkyl azides. Organized into 10 chapters, this book begins with an overview of the properties and chemistry of alkyl azides and alkylnitrenes. This text then examines the various pathways to the preparation of vinyl azides. Other chapters consider the magnetic resonance spectrum of phenyl azide, which may be taken as a representative to which more complex examples can be related. This book discusses as well the acyl azides and acylnitrenes that have their nitrogen function attached to electron-withdrawing groups not possessing a heteroatom bearing an unshared electron pair next to the nitrogen function. The final chapter deals with the main uses for organic azides involved in photochemical cross-linking of polymeric systems. This book is a valuable resource for chemists, spectroscopists, and theoreticians.


Nitrogenation Strategy for the Synthesis of N-containing Compounds

Nitrogenation Strategy for the Synthesis of N-containing Compounds

Author: Ning Jiao

Publisher: Springer

Published: 2016-11-15

Total Pages: 221

ISBN-13: 9811028133

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This book focuses on direct nitrogenation strategies to incorporate one or more N-atoms into simple substrates especially hydrocarbons via C–H and/or C–C bond cleavage, which is a green and sustainable way to synthesize nitrogen-containing compounds. The book consists of seven chapters demonstrating interesting advances in the preparation of amines, amides, nitriles, carbamides, azides, and N-heterocyclic compounds and illustrating the mechanisms of these novel transformations. It offers an accessible introduction to nitrogenation reactions for chemists involved in N-compound synthesis and those interested in discovering new reagents and reactions. Ning Jiao is a Professor of Chemistry at Peking University, China.


"One-pot" Synthesis of Organic Azides from Alcohols and Protected Sugars

Author: Charles Alan Hartranft

Publisher:

Published: 2008

Total Pages: 266

ISBN-13:

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This thesis deals with a novel "one-pot" synthesis of organic azides from simple alcohols as well as protected sugars. Experimentation led to the successful azidation of both classes of compounds while providing for the isolation and characterization of unexpected byproducts and side reactions. All findings were strongly supported by previous literature while yields of azide products isolated in this research were more than adequate.