Paper
Nickel-catalyzed [3+2+2] cycloaddition of ethyl cyclopropylideneacetate and diynes. Synthesis of 7,6- and 7,5-fused bicyclic compounds
Published Apr 30, 2007 · Kyotaro Maeda, S. Saito
Tetrahedron Letters
Q3 SJR score
39
Citations
0
Influential Citations
Abstract
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Study Snapshot
Nickel-catalyzed [3+2+2] cycloaddition of ethyl cyclopropylideneacetate and diynes effectively synthesizes 7,6- and 7,5-fused bicyclic compounds in good yields.
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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References
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Rhodium-catalyzed enantioselective cycloaddition of 1,6-enynes with cyclopropylideneacetamides produces bicyclic (cyclopent-2-en-1-ylidene)acetamides with high enanti
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