Mechanochemical Synthesis and Functionalization of Oxadiazo[2.2.2]octenes Through Oxidative Nitroso Diels–Alder Reaction and Hetero‐Cope Rearrangement

ABSTRACT The present work reports a straightforward approach for the mechanochemical oxidative nitroso Diels–Alder (DA) reaction for the rapid synthesis of oxadiazo[2.2.2]octenes and a mechanochemical [3+3] hetero‐Cope rearrangement to access the corresponding dioxazines within reduced reaction time (up to 1.5 min and 1.5 h, respectively), high yields and reproducibility toward different functional groups.

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Publication Details

Journal
Asian Journal of Organic Chemistry
Published
2026-09-30
DOI
https://doi.org/10.1002/ajoc.70557
Primary Topic
Crystallography and molecular interactions
Type
article
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article

Mechanochemical Synthesis and Functionalization of Oxadiazo[2.2.2]octenes Through Oxidative Nitroso Diels–Alder Reaction and Hetero‐Cope Rearrangement

Fabio Bellina, Antonio Del Vecchio, Mauro Pineschi, Marco Lessi et al.
Asian Journal of Organic Chemistry
Crystallography and molecular interactions
article

Mechanochemical Synthesis and Functionalization of Oxadiazo[2.2.2]octenes Through Oxidative Nitroso Diels–Alder Reaction and Hetero‐Cope Rearrangement

Fabio Bellina, Antonio Del Vecchio, Mauro Pineschi, Marco Lessi, Caterina Campinoti, Simona Marchetti
article en

Abstract

ABSTRACT The present work reports a straightforward approach for the mechanochemical oxidative nitroso Diels–Alder (DA) reaction for the rapid synthesis of oxadiazo[2.2.2]octenes and a mechanochemical [3+3] hetero‐Cope rearrangement to access the corresponding dioxazines within reduced reaction time (up to 1.5 min and 1.5 h, respectively), high yields and reproducibility toward different functional groups.

Asian Journal of Organic ChemistryVol. 15(10)
University of Pisa (IT), Consorzio Interuniversitario Reattività Chimica e Catalisi (IT)
Openalex Percentile: Top 13%
Crystallography and molecular interactions
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