7689-02-3Relevant articles and documents
Total Synthesis of (+)-Aspidospermidine
Xu, Hongjin,Huang, He,Zhao, Cui,Song, Chuanjun,Chang, Junbiao
, p. 6457 - 6460 (2019/09/06)
A facile asymmetric total synthesis of (+)-aspidospermidine has been developed, which is accomplished in 11 steps in an overall yield of 9.6%. Key steps involve a palladium-catalyzed enantioselective decarboxylative allylation to install the quaternary ca
Total Synthesis of (-)-Rhazinilam and Formal Synthesis of (+)-Eburenine and (+)-Aspidospermidine: Asymmetric Cu-Catalyzed Propargylic Substitution
Shemet, Andrej,Carreira, Erick M.
, p. 5529 - 5532 (2017/10/25)
A total synthesis of (-)-rhazinilam and formal syntheses of (+)-eburenine and (+)-aspidospermidine that rely on a copper(I)-catalyzed asymmetric propargylic substitution as the key step are reported. A salient feature of the reaction is the asymmetric con
Chemical synthesis of aspidosperma alkaloids inspired by the reverse of the biosynthesis of the rhazinilam family of natural products
McMurray, Lindsay,Beck, Elizabeth M.,Gaunt, Matthew J.
, p. 9288 - 9291 (2012/10/30)
Pyrrole reduction: Iterative metal-catalyzed C-H functionalization reactions facilitated the preparation of a highly substituted pyrrole derivative. This derivative could be transformed into the pyrrole-containing secondary metabolite, rhazinilam, which could in turn be transformed through a reductive transannular cascade process into the structurally complex pyrrolidine-containing alkaloid natural product, aspidospermidine.
