Paper
Triallyl(aryl)silanes serve as a convenient agent for silicon-based cross-coupling reaction of aryl halides
Published Dec 7, 2003 · Y. Nakao, Takuro Oda, A. Sahoo
Journal of Organometallic Chemistry
Q3 SJR score
31
Citations
0
Influential Citations
Abstract
Abstract hidden due to publisher request; this does not indicate any issues with the research. Click the full text link above to read the abstract and view the original source.
Study Snapshot
Triallyl(aryl)silanes efficiently cross-couple aryl bromides with a palladium catalyst and tetrabutylammonium fluoride, yielding a wide variety of functional groups and a high efficiency.
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
Full text analysis coming soon...
References
···
···
···
···
Citations
···
···
···
···