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Green Analysis of the Bromination Reaction of Propiophenone Derivatives Mediated by Cu 2+ Complexes

Article

Authorship
Krapacher, Claudio R. ; ROSSI, LAURA ISABEL
Date
2020
Publishing House and Editing Place
Wiley-VCH
Magazine
ChemistrySelect, vol. 5 (pp. 4740-4747) - ISSN 2365-6549
Wiley-VCH
ISSN
2365-6549
Summary Information provided by the agent in SIGEVA
All processes and reactions were evaluated using green metrics.Alternatives for the α-halogenation reaction of ketones were studied, varying both the methodology and the brominating reactants. CuBr2 and its complexes with organic ligands derived from biomass were used as bromide source. Distinct regioselectivity and chemoselectivity were observed with the different complexes used. The CuBr2-βCD complex behave completely different to the rest of the complexes since the halogenation oc... All processes and reactions were evaluated using green metrics.Alternatives for the α-halogenation reaction of ketones were studied, varying both the methodology and the brominating reactants. CuBr2 and its complexes with organic ligands derived from biomass were used as bromide source. Distinct regioselectivity and chemoselectivity were observed with the different complexes used. The CuBr2-βCD complex behave completely different to the rest of the complexes since the halogenation occurred preferentially in the propiophenone aromatic ring.Among the complexes used, novel starch and chitosan complexes with CuBr2 were synthesized and characterized by EPR, FT-IR, UVV RD and TGA.
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Key Words
COPPER COMPLEXESSYNTHETIC METHODSHALOGENATIONGREEN METRICSCYCLODEXTRINS