Please use this identifier to cite or link to this item:
https://dspace.ncfu.ru/handle/123456789/31112| Title: | Synthesis of Dimethyl (Z)-((3-oxoindolin-2-ylidene) (aryl)methyl)phosphonates Through Tandem Cadogan and Arbuzov Reactions |
| Authors: | Aksenov, N. A. Аксенов, Н. А. Aksenov, D. A. Аксенов, Д. А. Ganusenko, D. D. Ганусенко, Д. Д. Kurlikov, A. E. Курликов, А. Э. Barbolin, A. P. Барболин, А. П. Karaseva, P. S. Карасева, П. С. Aksenov, A. V. Аксенов, А. В. |
| Keywords: | Arbuzov reaction;Phosphonates;Cadogan–Sundberg reaction;Indoles;Chalcones;Phosphites;Reduction |
| Issue Date: | 2025 |
| Publisher: | Multidisciplinary Digital Publishing Institute (MDPI) |
| Citation: | Aksenov N.A., Aksenov D.A., Ganusenko D.D., Kurlikov A.E., Barbolin A.P., Karaseva P.S., Aksenov A.V. Synthesis of Dimethyl (Z)-((3-oxoindolin-2-ylidene) (aryl)methyl)phosphonates Through Tandem Cadogan and Arbuzov Reactions // MolBank. - 2025. - 2025 (2). - art. no. M2002. - DOI: 10.3390/M2002 |
| Series/Report no.: | MolBank |
| Abstract: | A novel method employing a tandem Cadogan and Arbuzov reaction sequence has been developed, providing access to a series of previously unreported dimethyl (Z)-((3-oxoindolin-2-ylidene)(aryl)methyl)phosphonates. Restricted rotation of the aryl substituent, particularly in the presence of ortho substituents, gives axial chirality to these compounds. |
| URI: | https://dspace.ncfu.ru/handle/123456789/31112 |
| Appears in Collections: | Статьи, проиндексированные в SCOPUS, WOS |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| scopusresults 3623.pdf Restricted Access | 128.95 kB | Adobe PDF | View/Open | |
| WoS 2167.pdf Restricted Access | 111.28 kB | Adobe PDF | View/Open |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.