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http://hdl.handle.net/123456789/2302Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Singh, Gurpreet | - |
| dc.contributor.author | Goswami, P. | - |
| dc.contributor.author | Anand, R.V. | - |
| dc.date.accessioned | 2020-11-27T04:19:19Z | - |
| dc.date.available | 2020-11-27T04:19:19Z | - |
| dc.date.issued | 2018 | - |
| dc.identifier.citation | Organic and Biomolecular Chemistry, 16(3), pp. 384-388 | en_US |
| dc.identifier.other | https://doi.org/10.1039/C7OB02882B | - |
| dc.identifier.uri | https://pubs.rsc.org/en/content/articlelanding/2018/ob/c7ob02882b#!divAbstract | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/2302 | - |
| dc.description.abstract | Bis-(amino)cyclopropenylidene has been utilised as a non-covalent Brønsted base catalyst in the 1,6-conjugate addition of carbon nucleophiles to p-QMs. This protocol makes it possible to access unsymmetrical diaryl- and triarylmethanes in good to excellent yields. Further, this catalyst was also explored in the 1,4-conjugate addition of carbon nucleophiles to enone systems | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Royal Society of Chemistry | en_US |
| dc.subject | Cyclopropenylidenes | en_US |
| dc.subject | Non-covalent | en_US |
| dc.subject | Carbon nucleophiles | en_US |
| dc.subject | Nucleophiles | en_US |
| dc.title | Exploring bis-(amino)cyclopropenylidene as a non-covalent Brønsted base catalyst in conjugate addition reactions | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | Research Articles | |
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| File | Description | Size | Format | |
|---|---|---|---|---|
| Need to add pdf.odt | 8.63 kB | OpenDocument Text | View/Open |
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