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Oxidative addition ofN-aminophthalimide to conjugated azoalkenes. Synthesis of the first C-azoaziridines

✍ Scribed by M. A. Kuznetsov; L. M. Kuznetsova; J. Schantl

Book ID
110666391
Publisher
SP MAIK Nauka/Interperiodica
Year
2000
Tongue
English
Weight
602 KB
Volume
36
Category
Article
ISSN
1023-1935

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ChemInform Abstract: Oxidative Addition
ChemInform Abstract: Oxidative Addition of N-Aminophthalimide to Conjugated Azoalkenes. Synthesis of the First C-Azoaziridines.
✍ M. A. Kuznetsov; L. M. Kuznetsova; J. Schantl πŸ“‚ Article πŸ“… 2001 πŸ› John Wiley and Sons βš– 34 KB πŸ‘ 2 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a β€œFull Text” option. The original article is trackable v

Oxidative addition of N-aminophthalimide
Oxidative addition of N-aminophthalimide to thiophene and selenophene: the first example of a 5-thia(seleno)-3,7-diazatricyclo[4.1.0.02,4]heptane system
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The first examples of condensed saturated heterocycles containing a central tricyclic bisaziridine core were obtained by oxidative addition of N-aminophthalimide to thiophene and selenophene. Their structures and spectral features are described.