Klaus Banert 
Science of Synthesis: Houben-Weyl Methods of Molecular Transformations Vol. 41 [EPUB ebook] 
Nitro, Nitroso, Azo, Azoxy, and Diazonium Compounds, Azides, Triazenes, and Tetrazenes

Ajutor

Science of Synthesis: Houben-Weyl Methods of Molecular Transformations is the entirely new edition of the acclaimed reference series Houben-Weyl, the standard synthetic chemistry resource since 1909. This new edition is published in English and will comprise 48 volumes published between the years 2000 and 2008.


Science of Synthesis is a quality reference work developed by a highly esteemed editorial board to provide a comprehensive and critical selection of reliable organic and organometallic synthetic methods. This unique resource is designed to be the first point of reference when searching for a synthesis strategy.



  • Contains the expertise of presently 400 leading chemists worldwide

  • Critically evaluates the preparative applicability and significance of the synthetic methods

  • Discusses relevant background information and provides detailed experimental procedures


For full information on the Science of Synthesis series, visit the Science of Synthesis Homepage

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<p>41.1 Product Class 1: Nitroalkanes<br>41.2 Product Class 2: Nitrosoalkanes and Nitroso Acetals (<em>N</em>, <em>N</em>-Dialkoxyamines)<br>41.3 Product Class 3: <em>N</em>-Nitroamines<br>41.4 Product Class 4: <em>N</em>-Nitrosoamines<br>41.5 Product Class 5: Aliphatic Azoxy Compounds (Aliphatic Diazene Oxides)<br>41.6 Product Class 6: Aliphatic Azo Compounds<br>41.7 Product Class 7: Diazonium Compounds<br>41.8 Product Class 8: Azidoalkanes<br>41.9 Product Class 9: Alkyltriazenes<br>41.10 Product Class 10: Alkyltetrazenes<br>41.11 Product Class 11: <em>N</em>, <em>N</em>-Dihaloamines</p>
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Limba Engleză ● Format EPUB ● Pagini 770 ● ISBN 9783131783813 ● Mărime fișier 30.0 MB ● Editor Klaus Banert ● Editura Thieme ● Oraș Stuttgart ● Țară DE ● Publicat 2014 ● Ediție 1 ● Descărcabil 24 luni ● Valută EUR ● ID 3140736 ● Protecție împotriva copiilor DRM social

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