Journal
ORGANOMETALLICS
Volume 34, Issue 8, Pages 1597-1600Publisher
AMER CHEMICAL SOC
DOI: 10.1021/om501170z
Keywords
-
Categories
Funding
- Manasaki Foundation
- Onassis Foundation
Ask authors/readers for more resources
The Au/TiO2-catalyzed reaction between 1,1,2,2-tetramethyldisilane and terminal alkynes yields substituted 1,4-disila-2,5-cyclohexadienes (1,1,4,4-tetramethyl-1,4-dihydro-1,4-disilines) in moderate to good yields. The reaction proceeds via initial SiSi activation of disilane by gold nanoparticles to form with alkynes isolable cis-1,2-disilyl adducts (cis-1,2-bis(dimethylsilyl)ethenes), which, under the reaction conditions, undergo a Au-catalyzed dehydrogenative cycloaddition to a second alkyne molecule, forming the final cycloadducts.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available