Paper
Synthesis of 2,6-diaryl-3-(trifluoromethyl)pyridines by regioselective Suzuki–Miyaura reactions of 2,6-dichloro-3-(trifluoromethyl)pyridine
Published Mar 27, 2013 · Shahzad Ahmed, M. Sharif, Khurram Shoaib
Tetrahedron Letters
Q3 SJR score
19
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
Regioselective Suzuki-Miyaura reactions can efficiently synthesize 2,6-diaryl-3-(trifluoromethyl)pyridines with different aryl substituents in a single-pot process without phosphane ligands.
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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