N-Heterocycle-coordinated λ5-iodanes as IBX alternatives for alcohol oxidations

Bibliografiske detaljer
Parent link:Chemical Communications.— .— Cambridge: RSC Publishing
Vol. 61.— 2025.— P. 756-759
Andre forfattere: Antonkin N. S. Nikita Sergeevich, Vlasenko Yu. A. Yuliya Aleksandrovna, Puylaert P. Pim, Nachtsheim B. J. Boris, Postnikov P. S. Pavel Sergeevich
Summary:Title screen
We report the synthesis of novel N-coordinated λ5-iodanes as a unique class of hypervalent iodine compounds. X-ray diffraction analysis revealed their intriguing (pseudo)cyclic structure, showcasing distinctive N⋯I-secondary bonding interactions. We demonstrate the in situ generation of reactive diacetoxy derivatives, which exhibits remarkable efficacy in alcohol oxidation reactions. Thermal stability assessments using TGA/DSC analysis provide crucial insights into the handling and potential applications of these compounds. This work expands the frontier of hypervalent iodine chemistry, offering new tools for selective oxidation reactions
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AM_Agreement
Sprog:engelsk
Udgivet: 2025
Fag:
Online adgang:https://doi.org/10.1039/D4CC05058D
Format: Electronisk Book Chapter
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=680718

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