
Please use this identifier to cite or link to this item:
http://hdl.handle.net/123456789/2253
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DC Field | Value | Language |
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dc.contributor.author | Mandal, S.K. | - |
dc.date.accessioned | 2020-11-26T06:13:00Z | - |
dc.date.available | 2020-11-26T06:13:00Z | - |
dc.date.issued | 2018 | - |
dc.identifier.citation | Organic and Biomolecular Chemistry, 16(17), pp. 3220-3228 | en_US |
dc.identifier.other | https://doi.org/10.1039/C8OB00586A | - |
dc.identifier.uri | https://pubs.rsc.org/en/content/articlelanding/2018/ob/c8ob00586a#!divAbstract | - |
dc.identifier.uri | http://hdl.handle.net/123456789/2253 | - |
dc.description | Only IISERM authors are available in the record. | - |
dc.description.abstract | An efficient, one-pot Cu-catalyzed tandem synthesis of fluorescent 1-benzyl-2-phenyl-1,2-dihydro-5H-chromeno[4,3-d]pyrimidin-5-ones from 4-chloro-3-formylcoumarin and benzylamines was developed by in situ intramolecular cross-dehydrogenative C(sp3)-N bond formation in moderate-to-good yields under ligand-free ambient conditions. This synthesis was easily scalable, and the generality of the substrates was established. These coumarin-fused pyrimidines exhibited interesting photo-physical properties and high quantum yields, and would be potential candidates for facilitating suitable studies in medicinal chemistry and materials science. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Royal Society of Chemistry | en_US |
dc.subject | Aromatic compounds | en_US |
dc.subject | Chemical bonds | en_US |
dc.subject | Fused pyrimidine | en_US |
dc.subject | Benzylamines | en_US |
dc.title | An unprecedented tandem synthesis of fluorescent coumarin-fused pyrimidines via copper-catalyzed cross-dehydrogenative C(sp3)–N bond coupling | en_US |
dc.type | Article | en_US |
Appears in Collections: | Research Articles |
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