## Abstract Protection of the terminal alkyne function in 1β(4βethynylphenyl)β4β(propβ2βenyl)β2,6,7βtrioxabicyclo[2.2.2]octane with a trimethylsilyl group permits the selective catalytic reduction of the olefin moiety with tritium gas to give after deprotection 1β(4βethynylphenyl)β4β[2,3β^3^H~2~]pr
(.+-.)-4-tert-Butyl-3-cyano-1-(4-ethynylphenyl)-2,6,7-trioxabicyclo[2.2.2]octane: synthesis of a remarkably potent GABAA receptor antagonist
β Scribed by Palmer, Christopher J.; Cole, Loretta M.; Casida, John E.
- Book ID
- 118010114
- Publisher
- American Chemical Society
- Year
- 1988
- Tongue
- English
- Weight
- 430 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0022-2623
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
The preparation of novel 3-(4-methyl-2,6,7-trioxabicyclo[2.2.2]octyl)-A2-isoxazolines 2 via nitrile oxide cycloaddition chemistry is described. The target compounds were produced in moderate to good yields using only 2.2 equivalents of alkene and without the need for slow addition of reagents. Cyclo
## 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