7.
A. F. Pozharskii*, V. A. Ozeryanskii, V. Y. Mikshiev, A. S. Antonov, A. V. Chernyshev, A. V. Metelitsa, G. S. Borodkin, N. S. Fedik, O. V. Dyablo
10-Dimethylamino derivatives of benzo[h]quinoline and benzo[h]quinazolines: fluorescent proton sponge analogues with opposed peri-NMe2/–N= groups. How to distinguish between proton sponges and pseudo-proton sponges
J. Org. Chem.
2016,
81,
5574–5587
,
DOI 6.
V. Y. Mikshiev, A. S. Antonov, A. F. Pozharskii*
Tandem synthesis of 10- dimethylaminobenzo[h]quinazolines from 2-ketimino-1,8-bis(dimethylamino)naphthalenes via nucleophilic replacement of the unactivated aromatic NMe2 group
Org. Lett.
2016,
18,
2872–2875
,
DOI 5.
A. S. Antonov, A. F. Pozharskii*, V. A. Ozeryanskii, A. Filarowski, K. Yu. Suponitsky, P. M. Tolstoy, M. A. Vovk
Ring lithiation of 1,8-bis(dimethylamino)naphthalene: another side of the „proton sponge coin”
Dalton Trans.
2016,
44,
17756–17766
,
DOI 4.
Kachalkina, G. S. Borodkin, A. F. Pozharskii*, A. S. Antonov, I. G. Borodkina, Y. F. Maltsev, E. A. Filatova, A. Filarowski, V. A. Ozeryanskii
Base-promoted transformation of 2-C(O)R-1,8-bis(dimethylamino)naphthalenes into benzo[g]indole derivatives
Mendeleev Commun.
2015,
25,
182–184
,
DOI 3.
A. S. Antonov, V. Y. Mikshiev, A. F. Pozharskii, V. A. Ozeryanskii*
Ortho-ketimines of 1,8-bis(dimethylamino)naphthalene: Synthesis, hydrolytic stability and transfer of basicity from proton sponge moiety to the imino function
Synthesis
2014,
46,
3273–3282
,
DOI 2.
V. A. Ozeryanskii, A. F. Pozharskii*, A. S. Antonov, A. Filarowski
Out-Basicity of 1,8-bis(dimethylamino)naphthalene: The experimental and theoretical challenge
Org. Biomol. Chem.
2014,
12,
2360–2369
,
DOI 1.
M. A. Povalyakhina, A. S. Antonov, O. V. Dyablo, V. A. Ozeryanskii, A. F. Pozharskii*
H-Bond-Assisted Intramolecular Nucleophilic Displacement of the 1-NMe2 Group in 1,8-Bis(dimethylamino)naphthalenes as a Route to Multinuclear Heterocyclic Compounds and Strained Naphthalene Derivatives
J. Org. Chem.
2011,
76,
7157-7166
,
DOI