![HALOGENATION OF N-ARYLSULFONYL-3-POLYCHLOROMETHYL-2- AZABICYCLO[2.2.1]HEPT-5-ENES](/upload/21232f297a57a5a743894a0e4a801fc3/issues/cover/f12c0f3d598d60e679936828022d0052.jpeg)
An approach to the preparation of new polyhalogenated N-sulfonylsubstituted azanorbornane derivatives, which are of interest as valuable reagents and promising biologically active substances, has been demonstrated
sulfonylimines, cyclopentadiene, azabicyclo[2.2.1]heptenes, halogenation, Wagner-Meerwein rearrangement.
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2. Bowers, A. M. Synthesis of highly substituted ureas and thioureas through 1,3-diaza-Claisen rearrangements / A. M. Bowers, J. S. Madalengoitia // Tetrahedron letters. - 2005. - Vol. 46. - P. 2869-2872.
3. Synthesis of a poly(2-azanorbornene) with a high degree of cis-TTstereoregularity and a regular secondary solutiostructure Rossegger, L. Olah, R. Fischer, P. Kaschnitz, O. Varga, M. Kallay, G. Scheipl, F. Stelzer, F. Wiesbrock // Polym. Chem. - 2012.
