Paper
Reaction of 2-trimethylsiloxy-1,3,2-oxazaphospholanes with phenol and ethanol
Published 1981 · L. K. Kibardina, Michael A. Pudovik, A. N. Pudovik
Bulletin of the Academy of Sciences of the USSR, Division of chemical science
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Abstract
ConclusionsThe reaction of 2-trimethylsiloxy-3-phenyl(methyl)-1,3,2-oxazaphospholanes with phenol or ethanol proceeds in two directions, with rupture of the endocyclic P-N bond and via desilylation of the starting phospholane. The end reaction products are alkylarylphosphorous acids.
Study Snapshot
The reaction of 2-trimethylsiloxy-1,3,2-oxazaphospholanes with phenol or ethanol produces alkylarylphosphorous acids through rupture of the endocyclic P-N bond and desilylation of the starting phospholane.
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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