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http://nopr.niscpr.res.in/handle/123456789/60824Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Hote, Baliram S | - |
| dc.contributor.author | Siddiqui, Tabassum A J | - |
| dc.contributor.author | Pisal, Parshuram M | - |
| dc.date.accessioned | 2022-11-11T09:51:58Z | - |
| dc.date.available | 2022-11-11T09:51:58Z | - |
| dc.date.issued | 2022-11 | - |
| dc.identifier.issn | 2583-1321 (Online); 0019-5103 (Print) | - |
| dc.identifier.uri | http://nopr.niscpr.res.in/handle/123456789/60824 | - |
| dc.description | 1184-1187 | en_US |
| dc.description.abstract | One of the synthetic intermediates is used in many organic transformations. A method for highly efficient synthesis of 1,1-diacetate (3a-j) from mixture of various substituted benzaldehydes and acetic anhydride under solvent- and catalyst free using visible light irradiation (150 W tungsten lamp) has been developed. The main advantages of this protocol includes shorter reaction time, eco-friendly, mild reaction condition, easy work-up procedures, high yields of products, are the attractive features of the present methodology. All synthesized 3a-j compounds were characterized by IR, 1H NMR and mass spectral analysis. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | NIScPR-CSIR, India | en_US |
| dc.source | IJC Vol.61(11) [Nov 2022] | en_US |
| dc.subject | 1,1-Diacetate | en_US |
| dc.subject | Visible light | en_US |
| dc.subject | Solvent- and catalyst free | en_US |
| dc.title | Solvent and catalyst free efficient chemoselective synthesis of 1,1-diacetate under visible light irradiation | en_US |
| dc.type | Article | en_US |
| dc.identifier.doi | https://doi.org/10.56042/ijc.v61i11.68267 | en_US |
| Appears in Collections: | IJC Vol.61(11) [Nov 2022] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJC 61(11) 1184-1187.pdf | 1.6 MB | Adobe PDF | View/Open |
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