Front Cover: Atroposelective Nenitzescu Indole Synthesis (Chem. Eur. J. 25/2023)
Chemistry - A European Journal(2023)
Abstract
For the helix-shaped vines growing in the garden, as well as for many bioactive molecules and other three-dimensional objects, chirality is an essential and ubiquitous property. The synthetic control of atropoisomerism along C−N bonds is particularly rare and challenging, however. A simple CrIII–salen complex was nevertheless used as a chiral enantiopure catalyst for a highly atroposelective Nenitzescu indole synthesis. More information can be found in the Research Article by F. W. Patureau and co-workers (DOI: 10.1002/chem.202300279).
MoreTranslated text
Key words
atroposelective nenitzescu indole synthesis
AI Read Science
Must-Reading Tree
Example
![](https://originalfileserver.aminer.cn/sys/aminer/pubs/mrt_preview.jpeg)
Generate MRT to find the research sequence of this paper
Chat Paper
Summary is being generated by the instructions you defined