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Unusual Formation of 2-Aryl-7,7-dimethyl-6,8-epidiseleno-5,6,7,8-tetrahydro-5-quinazolones

✍ Scribed by Natalija Tonkikh; Helmut Duddeck; Marina Petrova; Ojars Neilands; Andris Strakovs

Publisher
John Wiley and Sons
Year
1999
Tongue
English
Weight
196 KB
Volume
1999
Category
Article
ISSN
1434-193X

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✦ Synopsis

The selenious acid oxidation of 2-aryl-7,7-dimethyl-5,6,7,8-formation of an intramolecular unsymmetrical diselenide by selenious acid oxidation and reports the first derivatives of tetrahydro-5-quinazolones 2a-c leads to the corresponding 2-aryl-7,7-dimethyl-6,8-epidiseleno-5,6,7,8-tetrahydro-5-the new ring system 2,3-diselenabicyclo[3.2.1]octane. quinazolones 3a-c.

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