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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Dotsenko, V. V. | - |
| dc.contributor.author | Доценко, В. В. | - |
| dc.contributor.author | Aksenov, N. A. | - |
| dc.contributor.author | Аксенов, Н. А. | - |
| dc.contributor.author | Aksenova, I. V. | - |
| dc.contributor.author | Аксенова, И. В. | - |
| dc.date.accessioned | 2019-11-14T08:44:01Z | - |
| dc.date.available | 2019-11-14T08:44:01Z | - |
| dc.date.issued | 2019 | - |
| dc.identifier.citation | Dotsenko, V.V., Dushenko, V.A., Aksenov, N.A., Aksenova, I.V., Netreba, E.E. Unexpected Result of Thiophosphorylation of 6-Aminopyrano[2,3-c]pyrazole-5-carbonitrile Derivative // Russian Journal of General Chemistry. - 2019. - Volume 89. - Issue 9. - Pages 1752-1759 | ru |
| dc.identifier.uri | http://hdl.handle.net/20.500.12258/8339 | - |
| dc.description.abstract | The reaction of 6-amino-3-methyl-4-(2,4-dichlorophenyl)-2,4-dihydropyrano[2,3-c]pyrazole-5-carbonitrile with phosphorus sulfide in boiling pyridine unexpectedly leads to the formation of a not previously described heterocyclic system—[1,2]oxaphosphinino[6,5-c]pyrazole derivative. Structure of the obtained compound was proved using 2D NMR spectroscopy and X-ray diffraction analysis | ru |
| dc.language.iso | en | ru |
| dc.publisher | Pleiades Publishing | ru |
| dc.relation.ispartofseries | Russian Journal of General Chemistry | - |
| dc.subject | 1,2-oxaphosphinines | ru |
| dc.subject | Phosphorus(V) sulfide | ru |
| dc.subject | Pyrano[2,3-c]pyrazoles | ru |
| dc.subject | Thiophosphorylation | ru |
| dc.title | Unexpected result of thiophosphorylation of 6-aminopyrano[2,3-c]pyrazole-5-carbonitrile derivative | ru |
| dc.type | Статья | ru |
| vkr.amount | Pages 1752-1759 | ru |
| vkr.inst | Институт математики и естественных наук | - |
| Appears in Collections: | Статьи, проиндексированные в SCOPUS, WOS | |
Files in This Item:
| File | Size | Format | |
|---|---|---|---|
| scopusresults 1049 .pdf Restricted Access | 132.61 kB | Adobe PDF | View/Open |
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