Paper
Cycloaddition of 6-Hydroxy-2,6-dimethylcyclohexa-2,4-dienone: A Stereoselective Entry into Functionalized Bicyclo[2.2.2]octanes and a Novel 1,2-Migration of Methyl Group.
Published Dec 1, 2008 · Vishwakarma Singh, Girish Chandra, S. Mobin
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Abstract
Cycloaddition of 6-hydroxy-2,6-dimcthylcyclohexa-2,4-dienones with ethyl vinyl ether, butyl vinyl ether, vinyl acetate and vinyl phenyl sulphone leading to a stereoselective entry into bicyclo[2.2.2]octanes having quaternary methyl group is reported. A novel thermal 1,2-methyl migration has also been described.
Study Snapshot
This study demonstrates a novel 1,2-methyl migration in bicyclo[2.2.2]octanes by cycloaddition of 6-hydroxy-2,6-dimethylcyclohexa-2,4-dienones with ethyl vinyl ether, butyl vinyl ether
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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