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https://dspace.ncfu.ru/handle/20.500.12258/5437Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Demidov, O. P. | - |
| dc.contributor.author | Демидов, О. П. | - |
| dc.date.accessioned | 2019-05-20T13:34:47Z | - |
| dc.date.available | 2019-05-20T13:34:47Z | - |
| dc.date.issued | 2019 | - |
| dc.identifier.citation | Gutnov, A.V., Abaev, V.T., Demidov, O.P. Betti reaction of 2-naphthol, furfural, and acetamide: an unexpected case of secondary carbo-Piancatelli rearrangement // Chemistry of Heterocyclic Compounds. - 2019. - Volume 55. - Issue 3. - Pages 280-282 | ru |
| dc.identifier.uri | http://hdl.handle.net/20.500.12258/5437 | - |
| dc.description.abstract | Condensation of 2-naphthol, furfural, and acetamide in the presence of boric acid as acidic catalyst has led to Betti product N-[furan-2-yl(2-hydroxynaphthalen-1-yl)methyl]acetamide along with a new 10,10-dihydrocyclopenta[b]naphtho[1,2-d]furan derivative, which resulted from rare carbo-Piancatelli rearrangement. The structure is confirmed by 1 H, 13 C NMR, HRMS, and X-ray analyses. Mechanism of the transformation is discussed | ru |
| dc.language.iso | en | ru |
| dc.publisher | Springer New York LLC | ru |
| dc.relation.ispartofseries | Chemistry of Heterocyclic Compounds | - |
| dc.subject | 2-naphthol | ru |
| dc.subject | Betti reaction | ru |
| dc.subject | Boric acid | ru |
| dc.subject | Carbo-Piancatelli rearrangement | ru |
| dc.subject | Furfural | ru |
| dc.subject | Multicomponent reaction | ru |
| dc.title | Betti reaction of 2-naphthol, furfural, and acetamide: an unexpected case of secondary carbo-Piancatelli rearrangement | ru |
| dc.type | Статья | ru |
| vkr.amount | Pages 280-282 | ru |
| vkr.inst | Институт математики и естественных наук | - |
| Appears in Collections: | Статьи, проиндексированные в SCOPUS, WOS | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| WoS 588 .pdf Restricted Access | 75.41 kB | Adobe PDF | View/Open | |
| scopusresults 925 .pdf Restricted Access | 133.71 kB | Adobe PDF | View/Open |
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