Synthesis of (−)-julocrotine and a diversity oriented Ugi-approach to analogues and probes

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 precurso...

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Bibliographic Details
Main Authors: Ricardo A. W. Neves Filho, Bernhard Westermann, Ludger A. Wessjohann
Format: Article
Language:English
Published: Beilstein-Institut 2011-11-01
Series:Beilstein Journal of Organic Chemistry
Subjects:
Online Access:https://doi.org/10.3762/bjoc.7.175