Highly regioselective and sustainable solar click reaction: a new post- synthetic modified triazole organic polymer as a recyclable photocatalyst for regioselective azide- alkyne cycloaddition reaction
DC Field | Value | Language |
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dc.contributor.author | Dolly Yadav | - |
dc.contributor.author | Nem Singh | - |
dc.contributor.author | Tae Wu Kim | - |
dc.contributor.author | Jae Young Kim | - |
dc.contributor.author | No-Joong Park | - |
dc.contributor.author | Jin-Ook Baeg | - |
dc.date.available | 2019-09-04T06:06:30Z | - |
dc.date.created | 2019-06-17 | - |
dc.date.issued | 2019-05 | - |
dc.identifier.issn | 1463-9262 | - |
dc.identifier.uri | https://pr.ibs.re.kr/handle/8788114/6102 | - |
dc.description.abstract | The synthesis of pharmaceutically active 1,2,3-triazoles has been continuously scrutinized in the search for unique and effective catalysts to make the process efficient, green, and sustainable. Here, we are presenting a new visible light active Ni(ii) cyclam-integrated triazole-linked organic polymer (Ni-TLOP) photocatalyst for the synthesis of 1,2,3-triazole compounds with excellent efficiency and regioselectivity. The reaction was studied for a series of substrates and the absolute regioselectivity of a representative triazole product has also been confirmed by X-ray crystallography. The proficiency and chemical orthogonality of the Ni-TLOP are remarkable and it shows enhanced efficiency and regioselectivity. The use of a recyclable photocatalyst and non-hazardous reagents makes the catalytic system sustainable and environmentally friendly. This photocatalyzed click reaction technique has been successfully applied to the expedient synthesis of one of the most sold anti-epileptic drugs rufinamide. © The Royal Society of Chemistry 2019 | - |
dc.description.uri | 1 | - |
dc.language | 영어 | - |
dc.publisher | ROYAL SOC CHEMISTRY | - |
dc.title | Highly regioselective and sustainable solar click reaction: a new post- synthetic modified triazole organic polymer as a recyclable photocatalyst for regioselective azide- alkyne cycloaddition reaction | - |
dc.type | Article | - |
dc.type.rims | ART | - |
dc.identifier.wosid | 000468627800012 | - |
dc.identifier.scopusid | 2-s2.0-85066823488 | - |
dc.identifier.rimsid | 68452 | - |
dc.contributor.affiliatedAuthor | Tae Wu Kim | - |
dc.identifier.doi | 10.1039/c9gc00894b | - |
dc.identifier.bibliographicCitation | GREEN CHEMISTRY, v.21, no.10, pp.2677 - 2685 | - |
dc.citation.title | GREEN CHEMISTRY | - |
dc.citation.volume | 21 | - |
dc.citation.number | 10 | - |
dc.citation.startPage | 2677 | - |
dc.citation.endPage | 2685 | - |
dc.description.journalClass | 1 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.subject.keywordPlus | POROUS POLYMER | - |
dc.subject.keywordPlus | CO2 | - |
dc.subject.keywordPlus | EFFICIENT | - |
dc.subject.keywordPlus | 1,2,3-TRIAZOLES | - |
dc.subject.keywordPlus | CATALYST | - |
dc.subject.keywordPlus | NANOPARTICLES | - |
dc.subject.keywordPlus | CHEMISTRY | - |
dc.subject.keywordPlus | STORAGE | - |
dc.subject.keywordPlus | NETWORK | - |
dc.subject.keywordPlus | DESIGN | - |