On the cyclopropyl conjugation in benzo[a]spiro[2,5]octa-1,4-diene-3-one
β Scribed by P. Rys; P. Skrabal; H. Zollinger
- Publisher
- Elsevier Science
- Year
- 1971
- Tongue
- French
- Weight
- 89 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0040-4039
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π SIMILAR VOLUMES
Photolysis of benzo[a]spiro [2,5]octa-1,4-dien-3-one derivative 8a afforded spiro-fused tetracycles 10 as a pair of diastereomers in 1.7:1 ratio. The photochemical process occurred by cycloaddition of the intermediate-sulfone stabilized biradical 9 to the tethered olefin. Photolysis of dienone 8b ga
## 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 βFull Textβ option. The original article is trackable v
## Abstract The photoelectron spectra of spiro[3.4]octane (**1**), spiro[3.4]octeneβ5 (**2**), spiro[3.4]βoctaβ5,7βdiene (**3**), spiro[4.4]noneneβ2 (**4**) and spiro[4.4]nonaβ2,4βdiene (**5**) have been recorded. The first bands of these spectra are correlated with orbitals which are Οβorbitals, _