Biomimetic Iodofunctionalization of Aromatic and Heteroaromatic Compounds Catalyzed by Selenium Tetrachloride

Abstract A biomimetic iodofunctionalization of aromatic and heteroaromatic compounds has been developed using NaI as a source of iodine and 30% H2O2 as a mild oxidant, as well as SeCl4 as a commercially available catalyst in water without a co-solvent. The method affords iodinated compounds in isola...

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Main Authors: Beatriz C. O. Rocha, Givago P. Perecim, Cristiano Raminelli
Format: Article
Language:English
Published: Georg Thieme Verlag KG 2019-10-01
Series:SynOpen
Subjects:
Online Access:http://www.thieme-connect.de/DOI/DOI?10.1055/s-0039-1690337
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author Beatriz C. O. Rocha
Givago P. Perecim
Cristiano Raminelli
author_facet Beatriz C. O. Rocha
Givago P. Perecim
Cristiano Raminelli
author_sort Beatriz C. O. Rocha
collection DOAJ
description Abstract A biomimetic iodofunctionalization of aromatic and heteroaromatic compounds has been developed using NaI as a source of iodine and 30% H2O2 as a mild oxidant, as well as SeCl4 as a commercially available catalyst in water without a co-solvent. The method affords iodinated compounds in isolated yields of 37 to 99%. The catalytic system has potential for the bromination of aromatic substrates.
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spelling doaj.art-e4aebf73572e46a1975e11267bfbd93a2022-12-21T19:53:26ZengGeorg Thieme Verlag KGSynOpen2509-93962019-10-01030414214710.1055/s-0039-1690337Biomimetic Iodofunctionalization of Aromatic and Heteroaromatic Compounds Catalyzed by Selenium TetrachlorideBeatriz C. O. RochaGivago P. PerecimCristiano Raminelli0Instituto de Ciências Ambientais, Químicas e Farmacêuticas, Universidade Federal de São PauloAbstract A biomimetic iodofunctionalization of aromatic and heteroaromatic compounds has been developed using NaI as a source of iodine and 30% H2O2 as a mild oxidant, as well as SeCl4 as a commercially available catalyst in water without a co-solvent. The method affords iodinated compounds in isolated yields of 37 to 99%. The catalytic system has potential for the bromination of aromatic substrates.http://www.thieme-connect.de/DOI/DOI?10.1055/s-0039-1690337biomimetic synthesisiodofunctionalizationselenium catalysisiodinationaqueous reaction
spellingShingle Beatriz C. O. Rocha
Givago P. Perecim
Cristiano Raminelli
Biomimetic Iodofunctionalization of Aromatic and Heteroaromatic Compounds Catalyzed by Selenium Tetrachloride
SynOpen
biomimetic synthesis
iodofunctionalization
selenium catalysis
iodination
aqueous reaction
title Biomimetic Iodofunctionalization of Aromatic and Heteroaromatic Compounds Catalyzed by Selenium Tetrachloride
title_full Biomimetic Iodofunctionalization of Aromatic and Heteroaromatic Compounds Catalyzed by Selenium Tetrachloride
title_fullStr Biomimetic Iodofunctionalization of Aromatic and Heteroaromatic Compounds Catalyzed by Selenium Tetrachloride
title_full_unstemmed Biomimetic Iodofunctionalization of Aromatic and Heteroaromatic Compounds Catalyzed by Selenium Tetrachloride
title_short Biomimetic Iodofunctionalization of Aromatic and Heteroaromatic Compounds Catalyzed by Selenium Tetrachloride
title_sort biomimetic iodofunctionalization of aromatic and heteroaromatic compounds catalyzed by selenium tetrachloride
topic biomimetic synthesis
iodofunctionalization
selenium catalysis
iodination
aqueous reaction
url http://www.thieme-connect.de/DOI/DOI?10.1055/s-0039-1690337
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AT givagopperecim biomimeticiodofunctionalizationofaromaticandheteroaromaticcompoundscatalyzedbyseleniumtetrachloride
AT cristianoraminelli biomimeticiodofunctionalizationofaromaticandheteroaromaticcompoundscatalyzedbyseleniumtetrachloride