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Ring‐Opening Intramolecular Arylation of 1,2‐Disubtituted Epoxides with Tuneable Stereoselectivity.
- Source :
-
European Journal of Organic Chemistry . Mar2024, Vol. 27 Issue 9, p1-8. 8p. - Publication Year :
- 2024
-
Abstract
- A method of stereodivergent intramolecular ring‐opening arylation of amine‐tethered epoxides to 3,4‐disubstituted tetrahydroquinolines has been developed. The tuneable good stereoselectivity was attained by changing the catalyst from titanocene(III) catalyst to Lewis‐acidic zinc catalyst. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 1434193X
- Volume :
- 27
- Issue :
- 9
- Database :
- Academic Search Index
- Journal :
- European Journal of Organic Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 175799406
- Full Text :
- https://doi.org/10.1002/ejoc.202301271