Mild and efficient synthesis and base-promoted rearrangement of novel isoxazolo[4,5-b]pyridines

An efficient method for the synthesis of isoxazolo[4,5-b]pyridines has been developed on the basis of readily available 2-chloro-3-nitropyridines via the intramolecular nucleophilic substitution of the nitro group as a key step. The previously unknown base-promoted Boulton–Katritzky rearrangement of...

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Autors principals:	Vladislav V. Nikol’skiy, Mikhail E. Minyaev, Maxim A. Bastrakov, Alexey M. Starosotnikov
Format:	Artigo
Idioma:	Inglês
Publicat:	Beilstein-Institut 2024-05-01
Col·lecció:	Beilstein Journal of Organic Chemistry
Matèries:	aromatic nitro compounds boulton–katritzky rearrangement isoxazolo[4,5-b]pyridines nucleophilic substitution 1,2,3-triazoles
Accés en línia:	https://doi.org/10.3762/bjoc.20.94
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