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Publications in Math-Net.Ru |
Citations |
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2020 |
| 1. |
A. Petrenko, S. Belyakov, P. Arsenyan, “First examples of a covalent bond between gold and selenophene”, Mendeleev Commun., 30:5 (2020), 572–573   |
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2019 |
| 2. |
P. Arsenyan, J. Vasiljeva, A. Ivanova, S. Belyakov, “Unusual N,Se-heterocycles with cyclic Se–N<sup>+</sup> bond of isoselenazolopurinium type”, Mendeleev Commun., 29:1 (2019), 96–98 |
2
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2016 |
| 3. |
P. Arsenyan, J. Vasiljeva, S. Belyakov, M. Petrova, E. E. Liepin'sh, “Preparation and characterization of selenopheno[2,3-<i>b</i>]pyridine <i>N</i>-oxides”, Mendeleev Commun., 26:4 (2016), 317–319 |
5
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2015 |
| 4. |
P. Arsenyan, E. Paegle, S. Belyakov, “Microwave-assisted cyanation of 3-bromo-3-(1-hydroxyalkyl)benzo[<i>b</i>]selenophene derivatives”, Mendeleev Commun., 25:2 (2015), 119–120 |
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2014 |
| 5. |
P. Arsenyan, J. Vasiljeva, S. Belyakov, “Preparation of conjugated 6,6<i>’</i>-bibenzo[<i>b</i>]selenophenes”, Mendeleev Commun., 24:1 (2014), 32–34 |
19
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2011 |
| 6. |
P. Arsenyan, A. Petrenko, E. Paegle, S. Belyakov, “Direct N- and C-vinylation with trimethoxyvinylsilane”, Mendeleev Commun., 21:6 (2011), 326–328 |
12
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| 7. |
P. Arsenyan, A. Petrenko, J. Vasiljeva, S. Belyakov, “Reaction of selenium tetrabromide with ethynylpyridines”, Mendeleev Commun., 21:2 (2011), 80–81 |
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2009 |
| 8. |
B. Strumfs, E. E. Liepin'sh, S. Belyakov, P. T. Trapencieris, R. G. Kostyanovsky, “Reaction of diaziridine-3,3-dicarboxylic acid dihydrazide with acetone”, Mendeleev Commun., 19:2 (2009), 81–83 |
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| Organisations |
- Latvian Institute of Organic Synthesis, Riga, Latvian Republic
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