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Selective Diacetoxylation of Disubstituted 1,2,3-Triazoles through Palladium-Catalyzed C-H Activation.
- Source :
-
Synlett . 2018, Vol. 29 Issue 10, p1373-1378. 6p. - Publication Year :
- 2018
-
Abstract
- A simple and efficient selective diacetoxylation of 1,4-disubstituted 1,2,3-triazoles by Pd-catalyzed C-H bond activation is described. PhI(OAc)2 was used as an acetyloxy source to convert aromatic sp2 C-H bonds into C-O bonds with high selectivity by employing a 1,2,3-triazole ring as an elegant directing group. A range of 1,2,3-triazoles bearing two acetyloxy groups can be readily synthesized by the reaction. [ABSTRACT FROM AUTHOR]
- Subjects :
- *TRIAZOLES synthesis
*PALLADIUM catalysts
*CARBON-hydrogen bonds
Subjects
Details
- Language :
- English
- ISSN :
- 09365214
- Volume :
- 29
- Issue :
- 10
- Database :
- Academic Search Index
- Journal :
- Synlett
- Publication Type :
- Academic Journal
- Accession number :
- 129885718
- Full Text :
- https://doi.org/10.1055/s-0036-1591564