Paper
Synthesis and [3 + 2] Cycloaddition of a 2,2‐Dialkoxy‐1‐Methylenecyclopropane: 6,6‐Dimethyl‐1‐Methylene‐4,8‐Dioxaspiro[2.5]octane and cis‐5‐(5,5‐Dimethyl‐1,3‐Dioxan‐2‐ylidene)Hexahydro‐1(2H)‐Pentalen‐2‐one
Published Dec 12, 2003 · Masaharu Nakamura, X. Wang, M. Isaka
Organic Syntheses
UNKNOWN SJR score
4
Citations
0
Influential Citations
Abstract
2,2-Bis(chloromethyl)-5,5-dimethyl-1,3-dioxane 2-Cyclopenten-1-one 6,6-Dimethyl-1-methylene-4,8-dioxaspiro[2.5]octane 1,6,6-Trimethyl-4,8-dioxaspiro[2.5]oct-1-ene Keywords: substituted cyclopropenone acetal; alkylidene cyclopropanone acetal; dipolar trimethylenemethane; cycloaddition; cysteine protease inhibitor; biological activity; cycloadditions; electron acceptors
Study Snapshot
Cycloaddition of 2,2'-dialkoxy-1'-methylenecyclopropane to 1,6,6-Trimethyl-4,8-dioxaspiro[2.5]octane leads to a cysteine protease inhibitor with biological activity.
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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