Issue 9, 2022

Construction of azaspirocyclic skeletons mediated by the carbonyl of the Weinreb amide: formal total synthesis of (±)-cephalotaxine

Abstract

A facile Stevens rearrangement of the Weinreb amide and the subsequent key steps mediated by the carbonyl of the Weinreb amide led to the construction of azaspirocyclic skeletons of some typical alkaloids. And the formal total synthesis of (±)-cephalotaxine was completed via a shorter synthetic route by this efficient method. Further studies on the development and asymmetric synthesis application of this strategy are underway.

Graphical abstract: Construction of azaspirocyclic skeletons mediated by the carbonyl of the Weinreb amide: formal total synthesis of (±)-cephalotaxine

Supplementary files

Article information

Article type
Communication
Submitted
24 nov. 2021
Accepted
03 janv. 2022
First published
03 janv. 2022

Org. Biomol. Chem., 2022,20, 1879-1882

Construction of azaspirocyclic skeletons mediated by the carbonyl of the Weinreb amide: formal total synthesis of (±)-cephalotaxine

J. Liu, J. Zhang, Y. Fan, H. Ding, T. Liu, S. Li, M. Jiang and L. Liu, Org. Biomol. Chem., 2022, 20, 1879 DOI: 10.1039/D1OB02304G

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