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Updated: Jul 26, 2026

Efficient Construction of Drug-like Bispirocyclic Scaffolds Via Organocatalytic Cycloadditions of α-Imino γ-Lactones and Alkylidene Pyrazolones
Published on: February 7, 2019
A convergent approach to cyclopeptide alkaloids: total synthesis of sanjoinine G1
Taoues Temal-Laïb1, Jacqueline Chastanet, Jieping Zhu
1Institut de Chimie des Substances Naturelles, CNRS, 91198 Gif-sur-Yvette, France.
Abstract:
A general strategy for the synthesis of cyclopeptide alkaloids containing an endocyclic aryl-alkyl ether bond has been developed featuring a key intramolecular S(N)Ar reaction. The importance of the N-terminal protective group in the realization of such a strategy is documented. From the appropriate amino acid constituents, the natural sanjoinine G1, a 14-membered para cyclophane, has been synthesized in seven steps with 21% overall yield.
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