Transition-metal-free regioselective thiocyanation of phenols, anilines and heterocycles
| dc.contributor.author | Mete, Trimbak B. | en_US |
| dc.contributor.author | KHOPADE, TUSHAR M. | en_US |
| dc.contributor.author | BHAT, RAMAKRISHNA G. | en_US |
| dc.contributor.department | Dept. of Chemistry | en_US |
| dc.date.accessioned | 2019-07-01T05:32:46Z | |
| dc.date.available | 2019-07-01T05:32:46Z | |
| dc.date.issued | 2017-02 | en_US |
| dc.description.abstract | An expedient direct and regioselective thiocyanation of phenols, anilines and heterocycles is described. Transformation is realized via the direct CH functionalization under transition metal free conditions at ambient temperature in excellent yields. Method proved to be monoselective and variety of functional groups tolerated the reaction conditions. The practicality of the protocol is demonstrated in gram scale synthesis of a precursor of PPAR δ agonist in excellent yield. | en_US |
| dc.identifier.citation | Tetrahedron Letters, 58(5), 415-418. | en_US |
| dc.identifier.issn | 0040-4039 | en_US |
| dc.identifier.sourcetitle | Tetrahedron Letters | en_US |
| dc.identifier.uri | http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3197 | |
| dc.identifier.uri | https://doi.org/10.1016/j.tetlet.2016.12.043 | |
| dc.language.iso | en | en_US |
| dc.publication.originofpublisher | Foreign | en_US |
| dc.publisher | Elsevier B.V. | en_US |
| dc.subject | Transition metal free protocol | en_US |
| dc.subject | Radical pathway | en_US |
| dc.subject | Thiocyanation | en_US |
| dc.subject | Transition-metal-free | en_US |
| dc.subject | Persulphate | en_US |
| dc.subject | Radical cation | en_US |
| dc.subject | Radical scavenger | en_US |
| dc.subject | 2017 | en_US |
| dc.title | Transition-metal-free regioselective thiocyanation of phenols, anilines and heterocycles | en_US |
| dc.type | Article | en_US |