Pyrolysis Products of Some Pyrazolinodiazepines: Homodiazepines and Pyrazolopyridines
Author:
Affiliation:
1. Ecole Nationale Supérieure de Chimie, Université de Haute‐Alsace, F‐68093 Mulhouse Cédex, France
2. UFR de Physique Fondamentale, Université des Sciences et Techniques de Lille, F‐59655 Villeneuve d'Ascq Cédex, France
Publisher
Wiley
Subject
Inorganic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/cber.19871201103
Reference21 articles.
1. Chemospezifität und Regioselektivität bei der Cycloaddition von Diazoalkanen an 1 H ‐1,2‐Diazepine
2. Pyrazolino-diazepines and homodiazepines
3. Synthese und Struktur eines Cyclopropapyridins
4. Synthesis and Structure of a Cyclopropapyridine
5. By convention the direct adducts which are the major ones are those bearing a nitrogen atom at the 1‐position; the inverse adducts bear an sp3carbon atom in this position (homodiazepine 4 numbering).
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1. 2,2′-Bis-azonia-Cope Rearrangements of 2,3-Homo-6H-1,4-diazepinium Dications;European Journal of Organic Chemistry;2013-06-17
2. Some thoughts on choosing the correct space group;Acta Crystallographica Section B Structural Science;1995-12-01
3. Stereospecific Synthesis of 2-Oxazinyl-4-oxoazetidinecarbamates Starting from a 1,2-Diazepine. A new type of intramolecular transbenzoylation;Helvetica Chimica Acta;1988-06-15
4. ChemInform Abstract: Pyrolysis Products of Some Pyrazolinodiazepines: Homodiazepines and Pyrazolopyridines.;ChemInform;1988-02-02
5. A Torquospecific 1,5-Electrocyclization;Helvetica Chimica Acta;1987-12-16
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