Paper
Triphenylphosphine‐Catalyzed Dehydrogenative Coupling Reaction of Carboxylic Acids with Silanes – A Convenient Method for the Preparation of Silyl Esters
Published Apr 2, 2007 · Guo‐Bin Liu, Hong Zhao, T. Thiemann
Advanced Synthesis & Catalysis
22
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0
Influential Citations
Abstract
Triphenylphosphine has been found to be an efficient catalyst for the dehydrosilylation of carboxylic acids with silanes. In the presence of 4 mol% of triphenylphosphine (PPh 3 ), dehydrosilylation reactions in DMF afforded the corresponding silyl esters at 120 °C in good yield.
Study Snapshot
Triphenylphosphine is an efficient catalyst for dehydrosilylation of carboxylic acids with silanes, leading to the preparation of silyl esters at 120°C in good yield.
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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