Paper
Reactions of Substituted 2,3,7-Triazabicyclo[3.3.0]oct-3-ene-4-carboxylic Acid Esters with Halogens
Published 2001 · A. Molchanov, A. Stepakov, R. Kostikov
Russian Journal of Organic Chemistry
Q4 SJR score
5
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0
Influential Citations
Abstract
Substituted 2,3,7-triazabicyclo[3.3.0]oct-3-ene-4-carboxylic acid esters react with chlorine and bromine to give the corresponding 4-halo-2,3,7-triazabicyclo[3.3.0]oct-2-ene-4-carboxylates. Heating of the latter to 120°C under reduced pressure leads to elimination of nitrogen molecule and formation of 6-halo-3-azabicyclo[3.1.0]hexane-6-carboxylates.
Study Snapshot
Substituted 2,3,7-triazabicyclo[3.3.0]oct-3-ene-4-carboxylic acid esters react with chlorine and bromine to produce 4-halo-2,3,7-triazabicyclo[3.3.0]oct-2-ene-4-
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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