Paper
Evidence for a carbonium ion rearrangement in the reaction of triisobutylaluminum and 1,3,3-trimethylcyclopropene
Published 1981 · Herman G. Richey, Barry Kubala, Mark A. Smith
Tetrahedron Letters
8
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Abstract
Abstract hidden due to publisher request; this does not indicate any issues with the research. Click the full text link above to read the abstract and view the original source.
Study Snapshot
Carbonium ion rearrangement plays a role in the formation of acyclic products in the reaction of triisobutylaluminum and 1,3,3-trimethylcyclopropene, supporting the proposed mechanism for carbalumination of alkenes.
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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