N-Allyl-substituted aminomethylene-1,1-bisphosphonates in 1,3-dipolar cycloaddition reaction with aromatic nitrile N-oxides
- Authors: Bykhovskaya O.V.1, Aladzheva I.M.1, Brel V.K.1
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Affiliations:
- A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences
- Issue: Vol 66, No 7 (2017)
- Pages: 1256-1260
- Section: Full Articles
- URL: https://bakhtiniada.ru/1066-5285/article/view/240958
- DOI: https://doi.org/10.1007/s11172-017-1881-x
- ID: 240958
Cite item
Abstract
A reaction of N-allyl-substituted aminomethylene-1,1-bisphosphonates with aromatic nitrile N-oxides was used to obtain new aminomethylenebisphosphonates with one or two 3-arylisoxazoline rings at the nitrogen atom. NMR spectroscopy studies showed that the bisphosphonates with two isoxazoline fragments in the molecule exist in solution as a mixture of two diastereomers.
About the authors
O. V. Bykhovskaya
A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences
Author for correspondence.
Email: shipov@ineos.ac.ru
Russian Federation, 28 ul. Vavilova, Moscow, 119991
I. M. Aladzheva
A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences
Email: shipov@ineos.ac.ru
Russian Federation, 28 ul. Vavilova, Moscow, 119991
V. K. Brel
A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences
Email: shipov@ineos.ac.ru
Russian Federation, 28 ul. Vavilova, Moscow, 119991
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