Crystallographic characterization of a stable 7-phosphanorbornadiene-7-oxide: 2,3-benzo-1,4,5,6,7-pentaphenyl-7-phosphabicyclo[2.2.1] hepta-2,5-diene-7-oxide
β Scribed by Christine Gottardo; Stephen Fratpietro; Alan N. Hughes; Mark Stradiotto
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 158 KB
- Volume
- 11
- Category
- Article
- ISSN
- 1042-7163
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β¦ Synopsis
The stable 7-phosphanorbornadiene derivative, 2,3-benzo-1,4,5,6,7-pentaphenyl-7-phosphabicyclo[2.2.1]hepta-2,5-diene-7-oxide (1) was synthesized in 45% yield via the Diels-Alder reaction of pentaphenylphosphole oxide and benzyne. The reaction occurs specifically to give a single isomer, which was characterized by use of X-ray crystallography and 31
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Hexahydro-4a-methyl-7,7-diphenyl-1(2H)-naphthalenone. -A clean and efficient route to the hitherto not reported title compound (VIII) starting from the known 3-ethenylcyclohexanone (I) is given. The approach represents a general strategy for the synthesis of related 7,7-diarylhexahydronaphthalenone