N-Allyl-substituted aminomethylene-1,1-bisphosphonates in 1,3-dipolar cycloaddition reaction with aromatic nitrile N-oxides


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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.

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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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