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Synthesis of (-)-julocrotine and a diversity oriented Ugi-approach to analogues and probes
Ricardo A W Neves Filho1, Bernhard Westermann, Ludger A Wessjohann
1Department of Bioorganic Chemistry, Leibniz Institute of Plant Biochemistry, Weinberg 3, 06120 Halle, Germany.
Abstract:
An improved total synthesis of (-)-julocrotine in three steps from Cbz-glutamine, in 51% overall yield, is presented. To demonstrate the potential of the heterocyclic moiety for diversity oriented synthesis, a series of (-)-julocrotine analogues was synthesized by employing the heterocyclic precursor as an amino input in Ugi four-component reactions (Ugi-4CR) [1].
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