Paper
Regioselective C(sp2)-H dual functionalization of indoles using hypervalent iodine(III): bromo-amination via 1,3-migration of imides on indolyl(phenyl)iodonium imides.
Published Jan 27, 2015 · K. Moriyama, Kazuma Ishida, H. Togo
Chemical communications
Q1 SJR score
28
Citations
0
Influential Citations
Abstract
A regioselective C(sp(2))-H dual functionalization of indoles, which underlies bromo-amination via the 1,3-migration of imide groups on indolyl(phenyl)iodonium imides as novel imide-combined hypervalent iodines(III), has been developed to provide 2-bis(sulfonyl)amino-3-bromo-indoles under the metal-free conditions.
Study Snapshot
This regioselective C(sp2)-H dual functionalization of indoles using hypervalent iodine(III) allows for the production of 2-bis(sulfonyl)amino-3-bromo-indoles under metal-free conditions.
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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