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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | LONDHE, GOKUL S. | en_US |
| dc.contributor.author | MONDAL, SHANKHAJIT | en_US |
| dc.contributor.author | GNANAPRAKASAM, BOOPATHY | en_US |
| dc.date.accessioned | 2026-04-09T12:24:27Z | - |
| dc.date.available | 2026-04-09T12:24:27Z | - |
| dc.date.issued | 2025-08 | en_US |
| dc.identifier.citation | Chemical Communications, 61(62), 11617-11620. | en_US |
| dc.identifier.issn | 1364-548X | en_US |
| dc.identifier.uri | https://doi.org/10.1039/D5CC02950C | en_US |
| dc.identifier.uri | http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/10841 | - |
| dc.description.abstract | A Mn-catalysed efficient domino process for the synthesis of new C-3 substituted dihydrocoumarins from 2-hydroxybenzyl alcohols and 4-hydroxy-2H-chromen-2-ones under one-pot conditions is described. This reaction proceeds via a series of reactions in one-pot, such as o-quinone methide formation, Michael addition, intramolecular transesterification, and skeletal rearrangement to access dihydrocoumarins. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Royal Society of Chemistry | en_US |
| dc.subject | Chemistry | en_US |
| dc.subject | 2025 | en_US |
| dc.title | A Mn(iii)-catalysed domino process for C-3 substituted dihydrocoumarins from 2-hydroxybenzyl alcohols and 4-hydroxy-2H-chromen-2-ones | en_US |
| dc.type | Article | en_US |
| dc.contributor.department | Dept. of Chemistry | en_US |
| dc.identifier.sourcetitle | Chemical Communications | en_US |
| dc.publication.originofpublisher | Foreign | en_US |
| Appears in Collections: | JOURNAL ARTICLES | |
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