An Organocatalytic Regiospecific Synthesis of 1,5-Disubstituted 4-Thio-1,2,3-triazoles and 1,5-Disubstituted 1,2,3-Triazoles
An Organocatalytic Regiospecific Synthesis of 1,5-Disubstituted 4-Thio-1,2,3-triazoles and 1,5-Disubstituted 1,2,3-Triazoles
| dc.contributor.author | Ramachary, Dhevalapally B. | |
| dc.contributor.author | Krishna, Patoju M. | |
| dc.contributor.author | Gujral, Jagjeet | |
| dc.contributor.author | Reddy, G. Surendra | |
| dc.date.accessioned | 2022-03-27T09:39:05Z | |
| dc.date.available | 2022-03-27T09:39:05Z | |
| dc.date.issued | 2015-11-01 | |
| dc.description.abstract | Organocatalytic azide-ketone [3+2] cycloaddition (OrgAKC) of a variety of 1-aryl-2-(arylthio)ethanones and 1-alkyl-2-(alkylthio)ethanones with different aryl or alkyl azides is reported in dimethyl sulfoxide or solvent-free under ambient conditions to furnish 1,5-disubstituted 4-thio-1,2,3-triazoles in a regiospecific manner, which are further converted into useful 1,5-disubstituted 1,2,3-triazoles by treatment with Raney Ni at 25 ?C for 1-3 h. Notable features of the OrgAKC reaction include high rate and selectivity, solvent-free conditions, easily available substrates and catalysts, a wide range of synthetic and medicinal applications, and excellent yields generating a vast library of triazoles. | |
| dc.identifier.citation | Chemistry - A European Journal. v.21(47) | |
| dc.identifier.issn | 09476539 | |
| dc.identifier.uri | 10.1002/chem.201503302 | |
| dc.identifier.uri | https://onlinelibrary.wiley.com/doi/10.1002/chem.201503302 | |
| dc.identifier.uri | https://dspace.uohyd.ac.in/handle/1/13157 | |
| dc.subject | azides | |
| dc.subject | click chemistry | |
| dc.subject | heterocycles | |
| dc.subject | ketones | |
| dc.subject | organocatalysis | |
| dc.title | An Organocatalytic Regiospecific Synthesis of 1,5-Disubstituted 4-Thio-1,2,3-triazoles and 1,5-Disubstituted 1,2,3-Triazoles | |
| dc.type | Journal. Article | |
| dspace.entity.type |
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