Paper
Synthesis of methyl-1-(tert-butoxycarbonylamino)-2-vinylcyclopropanecarboxylate via a Hofmann rearrangement utilizing trichloroisocyanuric acid as an oxidant.
Published Jan 7, 2011 · Zackary D Crane, P. Nichols, T. Sammakia
The Journal of organic chemistry
Q2 SJR score
35
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0
Influential Citations
Abstract
A trichloroisocyanuric acid (TCCA) mediated Hofmann rearrangement was utilized to synthesize methyl-1-(tert-butoxycarbonylamino)-2-vinylcyclopropanecarboxylate. A variety of functional groups are tolerated in this reaction including vinyl, cyclopropyl, pyridyl, aryl, benzyl, and nitro groups.
Study Snapshot
This study demonstrates that trichloroisocyanuric acid-mediated Hofmann rearrangement can synthesize methyl-1-(tert-butoxycarbonylamino)-2-vinylcyclopropanecarboxylate with tolerance for various functional groups.
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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