|
|
|
Publications in Math-Net.Ru |
Citations |
|
2026 |
| 1. |
M. A. Zherebtsov, N. D. Anisimova, A. E. Tarakanova, M. V. Arsenyev, S. A. Chesnokov, “Moving of the tetramethylbutanediyl substituent over the catecholcarbaldehyde core”, Mendeleev Commun., 36:1 (2026), 117–119  |
|
2022 |
| 2. |
A. E. Tarakanova, M. A. Zherebtsov, M. V. Arsenyev, E. V. Baranov, S. A. Chesnokov, V. K. Cherkasov, “New tri-<i>tert</i>-alkyl substituted <i>o</i>-quinones of tetraline family”, Mendeleev Commun., 32:4 (2022), 540–542  |
3
|
|
2021 |
| 3. |
M. A. Zherebtsov, M. V. Arsenyev, E. V. Baranov, S. A. Chesnokov, V. K. Cherkasov, “Synthesis and structure of sterically hindered <i>o</i>-benzoquinone carboxylic acid”, Mendeleev Commun., 31:2 (2021), 268–270 |
2
|
| 4. |
S. K. Polyakova, T. V. Balashova, R. V. Rumyantcev, M. V. Arsenyev, G. K. Fukin, S. A. Chesnokov, “Utilizing <i>o</i>-quinone methide chemistry: synthesis of sterically hindered acridin-4-ols”, Mendeleev Commun., 31:2 (2021), 262–264 |
8
|
|
2019 |
| 5. |
E. R. Zhiganshina, M. V. Arsenyev, A. S. Shavyrin, E. V. Baranov, S. A. Chesnokov, “Trans-etherification of catechol-type benzylic ether with diols as a route to new sterically hindered bis-catechols”, Mendeleev Commun., 29:1 (2019), 91–93 |
9
|
|
2018 |
| 6. |
M. V. Arsenyev, T. V. Astaf'eva, E. V. Baranov, A. I. Poddel'sky, S. A. Chesnokov, “New sterically hindered bis-catechol, bis-<i>o</i>-quinone and its bis-triphenylantimony(v) bis-catecholate. 3,5-Di-<i>tert</i>-butyl-6-methoxymethylcatechol as alkylating agent”, Mendeleev Commun., 28:1 (2018), 76–78 |
19
|
|
2016 |
| 7. |
M. V. Arsenyev, E. V. Baranov, M. P. Shurygina, S. A. Chesnokov, G. A. Abakumov, “New sterically-hindered catechols/<i>o</i>-benzoquinones. Reduction of 4,6-di-<i>tert</i>-butyl-2,3-dihydroxybenzaldehyde”, Mendeleev Commun., 26:6 (2016), 552–554 |
19
|
|
2015 |
| 8. |
M. V. Arsenyev, E. V. Baranov, A. Yu. Fedorov, S. A. Chesnokov, G. A. Abakumov, “New bis-<i>o</i>-quinone with azine spacer and its cyclization into indazolo[2,1-<i>a</i>]indazole system”, Mendeleev Commun., 25:4 (2015), 312–314 |
26
|
|
| Organisations |
|
|
