CENTRAL to the consideration of mechanism in many of the transformations of molecules of the formula (CH),, has been tetracyclo[4.4.0.02"0 .05"]deca-3,8-diene (I).3a-g We describe here a degenerate isomerization of bicyclo-[4.?.2]deca-2,4,7,9-tetraene (II) which most strongly implicates I as an inte
Thermal Isomerization of 7,8-Diazabicyclo[4.2.2]deca-2,4,7,9-tetraene N-oxide to Benzaldehyde Oxime
β Scribed by Henrik Olsen
- Book ID
- 102252370
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- German
- Weight
- 287 KB
- Volume
- 65
- Category
- Article
- ISSN
- 0018-019X
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β¦ Synopsis
Abstract
Thermal transformation of 7,8βdiazabicyclo[4.2.2]decaβ2,4,7,9βtetraene Nβoxide (3) was observed, (Z)βbenzaldehyde oxime being the major product, with (E)βbenzaldehyde oxime as a minor product. NβOxide 3 was labeled with deuterium Ξ± to the oxidized Nβatom. The location of the deuterium label in the thermolysis products fitted one of two reasonable mechanisms.
π SIMILAR VOLUMES
is%= : The title compound which incorporates a strained bridgehead double and highly deformed cis and trans stilbene structures in bicyclo[4.2.2]decane ring system was synthesized in good yield as an air-sensitive substance. Some reactions pertinent to strain were examined.