posted on 2002-02-21, 00:00authored byMatthias Herdemann, Ali Al-Mourabit, Marie-Thérèse Martin, Christian Marazano
On the basis of a biogenetic proposal for explaining the biogenesis of manzamine A, the cycloaddition
of dihydropyridinium salt 26 with diene derivative 5 leads to adducts 27. These adducts, as well
as their related and previously described analogues 9, are now shown to be precursors of diene
derivatives such as 10, 13, and 28. Treatment of diene 32 with sodium azide resulted in a one-step
formation of the tricyclic imino derivative 34. This key intermediate was further transformed into
tricyclic derivative 40, which possesses the essential features of the ABC ring of manzamine A.