at Google ScholarTitle data
Katkevica, Sarmite ; Salun, Pavlo ; Jirgensons, Aigars:
Synthesis of 5-substituted 3-mercapto-1,2,4-triazoles via Suzuki–Miyaura reaction.
In: Tetrahedron Letters.
Vol. 54
(2013)
Issue 34
.
- pp. 4524-4525.
ISSN 0040-4039
DOI: https://doi.org/10.1016/j.tetlet.2013.06.067
Abstract in another language
3-Bromo- and 3-iodo-N,S-dibenzyl-5-mercapto-1,2,4-triazoles were prepared and demonstrated as versatile building blocks for Suzuki–Miyaura cross-coupling with aryl, heteroaryl, and vinyl boronic acid derivatives. Deprotection of the resulting coupling products provided 5-substituted-3-mercapto-1,2,4-triazoles in good overall yields. This represents a novel and convenient approach for the introduction of a 3-mercapto-1,2,4-triazole substructure into target compounds.
Further data
| Item Type: | Article in a journal |
|---|---|
| Refereed: | Yes |
| Keywords: | 5-Mercapto-1,2,4-triazoles; Suzuki–Miyaura cross-coupling; Benzyl protection; Deprotection |
| Institutions of the University: | Faculties > Faculty of Biology, Chemistry and Earth Sciences > Department of Biology > Chair Animal Ecology I Faculties Faculties > Faculty of Biology, Chemistry and Earth Sciences Faculties > Faculty of Biology, Chemistry and Earth Sciences > Department of Biology |
| Result of work at the UBT: | No |
| DDC Subjects: | 500 Science > 540 Chemistry |
| Date Deposited: | 14 Dec 2022 08:43 |
| Last Modified: | 14 Dec 2022 09:17 |
| URI: | https://eref.uni-bayreuth.de/id/eprint/73018 |