Antonov AS - Search Results

1

peri-Interactions in 1,8-bis(dimethylamino)naphthalene ortho-ketimine cations facilitate [1,5]-hydride shift: selective synthesis of 1,2,3,4-tetrahydrobenzo[h]quinazolines.

Mikshiev VY, Tolstoy PM, Puzyk AM, Kirichenko SO, Antonov AS. Mikshiev VY, et al. Among authors: antonov as. Org Biomol Chem. 2022 Jun 8;20(22):4559-4568. doi: 10.1039/d2ob00674j. Org Biomol Chem. 2022. PMID: 35593098

2

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.

Povalyakhina MA, Antonov AS, Dyablo OV, Ozeryanskii VA, Pozharskii AF. Povalyakhina MA, et al. Among authors: antonov as. J Org Chem. 2011 Sep 2;76(17):7157-66. doi: 10.1021/jo201171z. Epub 2011 Aug 11. J Org Chem. 2011. PMID: 21834514

3

Out-basicity of 1,8-bis(dimethylamino)naphthalene: the experimental and theoretical challenge.

Ozeryanskii VA, Pozharskii AF, Antonov AS, Filarowski A. Ozeryanskii VA, et al. Among authors: antonov as. Org Biomol Chem. 2014 Apr 21;12(15):2360-9. doi: 10.1039/c3ob41986j. Org Biomol Chem. 2014. PMID: 24522408

4

Ring lithiation of 1,8-bis(dimethylamino)naphthalene: another side of the 'proton sponge coin'.

Antonov AS, Pozharskii AF, Ozeryanskii VA, Filarowski A, Suponitsky KY, Tolstoy PM, Vovk MA. Antonov AS, et al. Dalton Trans. 2015 Oct 28;44(40):17756-66. doi: 10.1039/c5dt02482j. Epub 2015 Sep 23. Dalton Trans. 2015. PMID: 26399216

5

Tandem Synthesis of 10-Dimethylaminobenzo[h]quinazolines from 2-Ketimino-1,8-bis(dimethylamino)naphthalenes via Nucleophilic Replacement of the Unactivated Aromatic NMe2 Group.

Mikshiev VY, Antonov AS, Pozharskii AF. Mikshiev VY, et al. Among authors: antonov as. Org Lett. 2016 Jun 17;18(12):2872-5. doi: 10.1021/acs.orglett.6b01178. Epub 2016 Jun 3. Org Lett. 2016. PMID: 27258556

6

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.

Pozharskii AF, Ozeryanskii VA, Mikshiev VY, Antonov AS, Chernyshev AV, Metelitsa AV, Borodkin GS, Fedik NS, Dyablo OV. Pozharskii AF, et al. Among authors: antonov as. J Org Chem. 2016 Jul 1;81(13):5574-87. doi: 10.1021/acs.joc.6b00917. Epub 2016 Jun 20. J Org Chem. 2016. PMID: 27285083

7

1,8-Bis(dimethylamino)naphthyl-2-ketimines: Inside vs outside protonation.

Antonov AS, Pozharskii AF, Tolstoy PM, Filarowski A, Khoroshilova OV. Antonov AS, et al. Beilstein J Org Chem. 2018 Nov 28;14:2940-2948. doi: 10.3762/bjoc.14.273. eCollection 2018. Beilstein J Org Chem. 2018. PMID: 30546478 Free PMC article.

8

Proton-induced fluorescence in modified quino[7,8-h]quinolines: dual sensing for protons and π-donors.

Pozharskii AF, Ozeryanskii VA, Mikshiev VY, Chernyshev AV, Metelitsa AV, Antonov AS. Pozharskii AF, et al. Among authors: antonov as. Org Biomol Chem. 2019 Sep 21;17(35):8221-8233. doi: 10.1039/c9ob01391a. Epub 2019 Aug 22. Org Biomol Chem. 2019. PMID: 31436774

9

Unusual behaviour of the spin-spin coupling constant ¹J_CH upon formation of CHX hydrogen bond.

Tupikina EY, Denisov GS, Antonov AS, Tolstoy PM. Tupikina EY, et al. Among authors: antonov as. Phys Chem Chem Phys. 2020 Jan 28;22(4):1994-2000. doi: 10.1039/c9cp05964d. Epub 2020 Jan 9. Phys Chem Chem Phys. 2020. PMID: 31915781

10

How Strong is Hydrogen Bonding to Amide Nitrogen?

Mikshiev VY, Pozharskii AF, Filarowski A, Novikov AS, Antonov AS, Tolstoy PM, Vovk MA, Khoroshilova OV. Mikshiev VY, et al. Among authors: antonov as. Chemphyschem. 2020 Apr 2;21(7):651-658. doi: 10.1002/cphc.201901104. Epub 2020 Feb 6. Chemphyschem. 2020. PMID: 31953976

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