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Pd(II) - Catalysed Cyclisations of Aminoalkenitols. Dr. Peter Szolcsányi Department of Organic Chemistry S lovak U niversity of Technology Bratislava , Slovak Republic. Pd(II)-Catalysed chlorocyclisation and N , O -bicyclisation of polyhydroxylated aminoalkenitols.
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Pd(II)-Catalysed Cyclisationsof Aminoalkenitols Dr. Peter Szolcsányi Department of Organic Chemistry Slovak University of Technology Bratislava, Slovak Republic
Pd(II)-Catalysed chlorocyclisation and N,O-bicyclisation of polyhydroxylated aminoalkenitols
Where did the idea come from ? P. Szolcsányiet al.: Tetrahedron: Asymmetry 2000, 11, 2579-2597.
Mechanistic proposal of the Pd(II)/CuCl2-catalysed chloroaminocyclisation and bicyclisation
Synthesis of new analogues of iminoalditols P. Szolcsányi, T. Gracza: Tetrahedron 2006, 62, 8498-8502.
Conclusions • We have found a novel Pd(II)-catalysed halocyclisation and/or bicyclisation • of aminoalkenitols providing chloromethyl-piperidines and/or oxa- • azabicyclo[3.2.1]octanes • We have postulated the reaction mechanism explaining the observed • chemoselectivity • Both transformations were developed intoeffectivesynthetic methodologies • that were successfully employed in the total synthesis of new analogues of • glycosidase inhibitor 1-deoxynojirimycin
Acknowledgments Generous support Prof. Dr. Tibor Gracza HPLC Dr. Katarína Hroboňová NMR Dr. Naďa Prónayová IR Ms. Silvia Markusová MALDI Dr. Ivan Špánik Grant APVT-20-000904
Known precedents of Pd(II)/CuCl2-catalysed haloaminocyclisation yielding 6-membered azacycles