Аннотация:
The reaction of 2-azanorbornene derivatives with nitrile oxides (generated in situ by dehydrohalogenation of N-hydroxyimoyl halides) affords two regioisomers with the exo-arrangement of the isoxazoline ring.
Образец цитирования:
T. A. Solodovnikova, N. V. Zyk, A. Yu. Gavrilova, “Reaction of 2-azabicyclo[2.2.1]heptenes with nitrile oxides”, Mendeleev Commun., 32:4 (2022), 549–550
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc722
https://www.mathnet.ru/rus/mendc/v32/i4/p549
Эта публикация цитируется в следующих 2 статьяx:
Gulnur N. Chernysheva, Maxim D. Katerinich, Igor A. Ushakov, Tatiana N. Borodina, Vladimir I. Smirnov, Igor B. Rozentsveig, “Polyhalogenated 2‐Azabicyclo[2.2.1]heptanes from Polyhaloaldimines and Cyclopentadiene via Cycloaddition and Wagner‐Meerwein Rearrangement”, Asian J Org Chem, 13:7 (2024)
Alexandra N. Shilova, Nina S. Shatokhina, Evgeniy V. Kondrashov, “[3 + 2] Cycloaddition of nitrile oxides to dichloropropenes and 1,3‐dichlorobut‐2‐ene: A regioselectivity issue”, Journal of Heterocyclic Chem, 61:4 (2024), 556
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