Paper
A new pathway for the preparation of biologically active 2 substituted 1,5-dihydrobenzo[e][1,2,4]oxadiazepines and related compounds by palladium-catalyzed cyclization of amidoximes with o-iodobenzyl bromide or 2-bromo-3-chloromethylpyridine
Published Jun 17, 2012 · E. Abele,, L. Golomba, T. Beresneva
Arkivoc
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Abstract
A simple palladium-catalyzed one-pot synthesis of 2-substituted 1,5-dihydrobenzo[ e ][1,2,4]- oxadiazepines from corresponding ( E )-amidoximes and o -iodobenzyl bromide or 2-bromo-3-chloromethylpyridine is described. Of the derivatives prepared 2-[6-(quinolin-2-ylsulfanyl)- hexyl]-1,5-dihydrobenzo[ e ][1,2,4]oxadiazepine exhibits high activity on HT-1080 (hyman fibro-sarcoma) and MG-22A (mouse hepatoma) cancer cell lines.
Study Snapshot
Palladium-catalyzed one-pot synthesis of 2-substituted 1,5-dihydrobenzo[e][1,2,4]oxadiazepines demonstrates high activity against HT-1080 and MG-22A cancer cell lines.
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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