Intramolecular Schmidt Reaction: Applications in Natural Product Synthesis
DOI:
https://doi.org/10.2533/000942906777674714Keywords:
Alkaloids, Alkyl azides, Iminium ions, Lactams, Rearrangement, Tertiary amines, Total synthesisAbstract
The intramolecular Schmidt reaction was first described at the beginning of the 1990s and rapidly proved to be a powerful tool for the fast assembly of complex nitrogen-containing heterocycles. This review focuses on the application of this reaction in the synthesis of natural products and other biologically relevant compounds.Downloads
Published
2006-05-24
Issue
Section
Scientific Articles
License
Copyright (c) 2006 Swiss Chemical Society

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
How to Cite
[1]
Chimia 2006, 60, 276, DOI: 10.2533/000942906777674714.