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Relevant bibliographies by topics / Aryl azene oxides

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Academic literature on the topic 'Aryl azene oxides'

Author: Grafiati

Published: 18 May 2024

Last updated: 31 July 2025

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Journal articles on the topic "Aryl azene oxides"

1

Schipper, Derek J., Mohamed El-Salfiti, Christopher J. Whipp, and Keith Fagnou. "Direct arylation of azine N-oxides with aryl triflates." Tetrahedron 65, no. 26 (2009): 4977–83. http://dx.doi.org/10.1016/j.tet.2009.03.077.

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2

Kim, Doyoung, Hyewon Ju, Wooseok Lee, and Sungwoo Hong. "Photocatalytic 1,3-Oxyheteroarylation of Aryl Cyclopropanes with Azine N-oxides." Chemical Science, 2024. http://dx.doi.org/10.1039/d4sc06723a.

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Cyclopropanes, valuable C3 building blocks in organic synthesis, possess high strain energy and inherent stability. We present an efficient, environmentally benign 1,3-oxyheteroarylation of aryl cyclopropanes using azine N-oxides as bifunctional...

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3

Schipper, Derek J., Mohamed El-Salfiti, Christopher J. Whipp, and Keith Fagnou. "ChemInform Abstract: Direct Arylation of Azine N-Oxides with Aryl Triflates." ChemInform 40, no. 44 (2009). http://dx.doi.org/10.1002/chin.200944145.

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Dissertations / Theses on the topic "Aryl azene oxides"

1

Das, Purak. "Aryl azene oxides : synthesis, structure and mesogenic behaviour." Thesis, University of North Bengal, 2006. http://hdl.handle.net/123456789/870.

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2

Whipp, Christopher J. "Part 1: The Direct Arylation of Azine N-Oxides with Aryl Triflates Part 2: The Site-Selective Direct Arylation of Substituted Indoles." Thesis, University of Ottawa (Canada), 2010. http://hdl.handle.net/10393/28792.

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Part 1: The Direct Arylation of Azine N -Oxides with Aryl Triflates. Two sets of conditions for the palladium-catalyzed direct arylation of azine N-oxides with aryl triflates have been developed. Using palladium(II) acetate, a trialkylphosphine ligand, a carbonate base and pivalic acid, both mono- and diarylated azine N-oxides could be synthesized in good to excellent yields.* The reaction regioselectivity was examined for 3-substituted pyridine N-oxides, with arylation at C2 being favoured. The methodology was applied to the efficient formal synthesis of a biologically active diaryl pyridin

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