Paper
Synthesis of 3‐phenoxy‐1,3‐dihydro‐1‐isobenzofuranones by palladium‐catalyzed carbonylative cyclization of 2‐bromobenzaldehyde with phenols
Published Jul 1, 1999 · C. Cho, D. Baek, S. Shim
Journal of Heterocyclic Chemistry
Q3 SJR score
10
Citations
0
Influential Citations
Abstract
2-Bromobenzaldehyde reacts with phenols in acetonitrile under carbon monoxide pressure in the presence of a catalytic amount of bis(triphenylphosphine)palladium(II) chloride to afford the corresponding 3-phenoxy-1,3-dihydro-1-isobenzofuranones in high yields.
Study Snapshot
This method enables the synthesis of 3-phenoxy-1,3-dihydro-1-isobenzofuranones in high yields by catalyzing carbonylative cyclization of 2-bromobenzaldehyde with phenols under carbon monoxide pressure.
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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