Paper
Selective Reduction of Hydroxy Carbonyl to Carbonyl Compounds with Trialkylborane/Trifluoromethanesulfonic Acid
Published Jan 1, 1991 · G. Olah, A. Wu
Synthesis
2
Citations
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Influential Citations
Abstract
Triethyl- or triisopropylborane/trifluoromethanesulfonic (triflic) acid is a convenient reagent for the selective reduction of hydroxy substituted carboxylic acids, ketones and aldehydes to yield the corresponding carbonyl compounds. The scope of the reaction, experimental conditions and suggested mechanisms are discussed
Study Snapshot
Trialkylborane/trifluoromethanesulfonic acid selectively reduces hydroxy carbonyl to carbonyl compounds, offering potential applications in organic synthesis and pharmaceutical research.
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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