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The Chemistry of Vinyl, Allenyl, and Ethynyl Azides

Institute of Chemistry, Chemnitz University of Technology, Strasse der Nationen 62, 09111 Chemnitz, Germany [Pg.115]

Dedicated to Professor Helmut Quast on the occasion of his 75th birthday [Pg.115]

1 Introduction and Early Synthetic Methods for Vinyl Azides [Pg.115]

In the case of other vinyl halides with an electron acceptor in the j3-position, the generation of vinyl azides is often followed by rapid liberation of dinitrogen and formation of a five-membered aromatic heterocycle. In 1958, for example, treatment of nitro [Pg.115]

Organic Azides Syntheses and Applications Edited by Stefan Erase and Klaus Banert 2010 John Wiley Sons, Ltd. ISBN 978-0-470-51998-1 [Pg.115]


See other pages where The Chemistry of Vinyl, Allenyl, and Ethynyl Azides is mentioned: [Pg.115]    [Pg.117]    [Pg.119]    [Pg.121]    [Pg.123]    [Pg.125]    [Pg.127]    [Pg.129]    [Pg.131]    [Pg.133]    [Pg.135]    [Pg.137]    [Pg.139]    [Pg.141]    [Pg.143]    [Pg.145]    [Pg.147]    [Pg.149]    [Pg.151]    [Pg.153]    [Pg.155]    [Pg.157]    [Pg.159]    [Pg.161]    [Pg.163]    [Pg.165]   


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Allenyl

Allenyl azides

Allenylation

Azide chemistry

Ethynyl azides

Ethynylation

Ethynyls

The Vinyls

Vinyl azide

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