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http://hdl.handle.net/123456789/2739Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Sastry, S.S.V.Rama | - |
| dc.date.accessioned | 2020-12-07T07:23:23Z | - |
| dc.date.available | 2020-12-07T07:23:23Z | - |
| dc.date.issued | 2014 | - |
| dc.identifier.citation | Angewandte Chemie - International Edition, 53(52), pp.14310-14312. | en_US |
| dc.identifier.other | 10.1002/anie.201409410 | - |
| dc.identifier.uri | https://onlinelibrary.wiley.com/doi/full/10.1002/anie.201409410 | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/2739 | - |
| dc.description.abstract | Recent advances in the metal‐free enamine/enolate‐mediated azide–carbonyl [3+2] cycloaddition reaction are discussed. These approaches require neither a metal catalyst nor alkyne substrates. Owing to the ready availability of carbonyl compounds, these methods thus offer excellent alternatives for the synthesis of 1,4‐/1,5‐disubstituted and 1,4,5‐trisubstituted 1,2,3‐triazoles. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Wiley-VCH Verlag | en_US |
| dc.subject | 1,2,3‐triazoles | en_US |
| dc.subject | Amines | en_US |
| dc.subject | Azides | en_US |
| dc.subject | Organocatalysis | en_US |
| dc.title | Enamine/enolate-mediated organocatalytic azide- Carbonyl [3+2] cycloaddition reactions for the synthesis of densely functionalized 1,2,3-triazoles | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | Research Articles | |
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|---|---|---|---|---|
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