V. A. Ozeryanskii

发表

Multiple transformations of 2-alkynyl-1,8-bis(dimethylamino)naphthalenes into benzo[g]indoles. Pd/Cu-dependent switching of the electrophilic and nucleophilic sites in acetylenic bond and a puzzle of porcelain catalysis.

E. Filatova, A. Gulevskaya, A. F. Pozharskii, 2015, The Journal of organic chemistry.

The first proton sponge-based amino acids: synthesis, acid-base properties and some reactivity.

A. F. Pozharskii, V. A. Ozeryanskii, A. Y. Gorbacheva, 2015, Organic & biomolecular chemistry.

Electrophilic Substitution in 5,6‐Bis(dimethylamino)acenaphthylene as a Route to Push‐Pull Proton Sponges.

A. F. Pozharskii, V. A. Ozeryanskii, M. A. Mekh, 2010 .

peri-Naphthylenediamines. 32. Reactions of 4,5-bis(dimethylamino)-1-naphthyllithium and 4,5-bis(dimethylamino)-1-naphthylmagnesium bromide with electrophilic agents. New representatives of double naphthalene “proton sponges” with the structures of 1,1"-binaphthyl ketone and 1,1"-binaphthylmethanol

A. F. Pozharskii, N. V. Vistorobskii, V. A. Ozeryanskii, 2001 .

Nucleophilic Substitution of Hydrogen Atom in Initially Inactivated Pyrrole Ring.

A. F. Pozharskii, G. S. Borodkin, A. Filarowski, 2019, Organic letters.

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

A. Antonov, P. Tolstoy, A. F. Pozharskii, 2015, Dalton transactions.

Positively and negatively charged NHN hydrogen bonds in one molecule: synergistic strengthening effect, superbasicity and acetonitrile capture

A. F. Pozharskii, O. Khoroshilova, V. A. Ozeryanskii, 2019, New Journal of Chemistry.

Ethynylene-Bridged para-ortho-para-Linked Proton Sponge Trimer: Mono- and Tris(tetrafluoroborate) Protic Salts, Crystal Structures, Color Effects, and HCONMe2/BF4– Hydrogen-Bond Discrimination

E. Filatova, A. Gulevskaya, A. F. Pozharskii, 2021, Crystal Growth & Design.

Neutral Pyrrole Nitrogen Atom as a π- and Mixed n,π-Donor in Hydrogen Bonding.

E. Filatova, A. F. Pozharskii, G. S. Borodkin, 2019, The Journal of organic chemistry.

Preparation of Dialkylamino-Substituted Benzenes and Naphthalenes by Nucleophilic Replacement of Fluorine in the Corresponding Perfluoroaromatic Compounds

J. Baker, M. Muir, V. Sorokin, 2006 .

Deuterium isotope effects on 15N, 13C and 1H chemical shifts of proton sponges

E. Grech, P. Hansen, M. Pietrzak, 2002 .

peri-Naphthylenediamines

A. F. Pozharskii, V. A. Ozeryanskii, V. Ozeryanskii, 1998 .

Novel Polyfunctional Tautomeric Systems Containing Salicylideneamino and Proton Sponge Moieties

L. Sobczyk, E. Grech, B. Kamieński, 2006 .

To what extent can a conjugation between two pairs of peri‐nitro and peri‐amino groups be realized through the naphthalene core?

E. Filatova, A. F. Pozharskii, V. Sorokin, 2013 .

Simple and hydrolytically stable proton sponge based organic cation displaying hydrogen bonding and a number of related phenomena

A. F. Pozharskii, V. A. Ozeryanskii, V. Ozeryanskii, 2013 .

‘Proton sponge’ amides: unusual chemistry and conversion into superbasic 6,7-bis(dimethylamino)perimidines

A. F. Pozharskii, V. A. Ozeryanskii, M. Vlasenko, 2013 .

Oxidation of 1-amino-4,5-bis(dimethylamino)naphthalene as a route to the double “proton sponges” based on dibenzo[a,h]phenazine and 1,1′-azonaphthalene

A. F. Pozharskii, V. A. Ozeryanskii, M. Vlasenko, 2011 .

Naphthalene proton sponges as hydride donors: diverse appearances of the tert-amino-effect.

A. F. Pozharskii, O. Kazheva, O. Dyachenko, 2011, Organic & biomolecular chemistry.

tert-Amino effect in naphthalene proton sponges: a novel approach to benzo[h]quinoline and quino[7,8:7’,8’]quinoline derivatives

A. F. Pozharskii, V. A. Ozeryanskii, O. Ryabtsova, 2010 .

Hexa- and heptasubstitution in the interaction of octafluoronaphthalene with lithium dialkylamides: a new approach to the naphthalene 'proton sponges'

A. F. Pozharskii, Z. Starikova, V. Sorokin, 2004 .

Electrophilic fluorination of N,N-dimethylaniline, N,N-dimethylnaphthalen-1-amine and 1,8-bis(dimethylamino)naphthalene with N–F reagents

A. F. Pozharskii, V. Sorokin, V. A. Ozeryanskii, 2013 .

5,6-Bis(dimethylamino)acenaphthylene as an activated alkene and 'proton sponge' in halogenation reactions

A. F. Pozharskii, V. A. Ozeryanskii, M. A. Mekh, 2006 .

N,N,N′-Trialkyl-1,8-diaminonaphthalenes: convenient method of preparation from protonated proton sponges and the first X-ray information

A. F. Pozharskii, O. Kazheva, O. Dyachenko, 2005 .

Base-promoted transformation of 2-C(O)R-1,8-bis(dimethylamino)naphthalenes into benzo[g]indole derivatives

A. Antonov, E. Filatova, A. F. Pozharskii, 2015 .

Three examples of naphthalene proton sponges with extreme or unusual structural parameters. General view on factors influencing proton sponge geometry

E. Filatova, A. F. Pozharskii, Z. Starikova, 2011 .

Proton-Sponge-Like Superbases Built on the Benzo[h ]quinoline Platform

A. F. Pozharskii, V. A. Ozeryanskii, V. Ozeryanskii, 2018, European Journal of Organic Chemistry.

Heterocyclic superbases: retrospective and current trends

E. Filatova, A. F. Pozharskii, V. A. Ozeryanskii, 2012, Chemistry of Heterocyclic Compounds.

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.

A. Antonov, A. F. Pozharskii, V. A. Ozeryanskii, 2011, The Journal of organic chemistry.

peri-Naphthylenediamines. 31. Study of interconversions of 2,3-dihydroperimidines and 1,8-bis(dialkylamino)naphthalenes. Convenient synthesis of 1,2,2,3-tetramethyl-2,3-dihydroperimidine and a monoisopropyl analog of the “proton sponge”

E. Filatova, A. F. Pozharskii, V. Sorokin, 2001 .

Synthesis of 2‐Aryl‐ and 2,7‐Diaryl‐1,8‐bis(dimethylamino)naphthalenes. Overview of the “Buttressing effect” in 2,7‐Disubstituted Proton Sponges

E. A. Ermolenko, E. Filatova, A. Gulevskaya, 2020 .

peri-naphthylenediamines

A. F. Pozharskii, N. V. Vistorobskii, V. A. Ozeryanskii, 2000 .

Organometallic Synthesis of 2,3,6,7-Tetrasubstituted 1,8-Bis(dimethylamino)naphthalenes for Investigation of the Double Buttressing Effect in Proton Sponges.

A. Antonov, A. F. Pozharskii, E. Y. Tupikina, 2022, The Journal of organic chemistry.

X-ray diffraction and IR-spectroscopic studies on protonated 4-amino-1,8-bis(dimethylamino)naphthalene

L. Sobczyk, E. Grech, A. F. Pozharskii, 2002 .

Extreme magnetic separation of geminal protons in protonated N,N,N'-trimethyl-1,8-diaminonaphthalene. A puzzle of the fourth methyl group.

A. F. Pozharskii, G. S. Borodkin, V. A. Ozeryanskii, 2013, Organic letters.

1,8-Bis(dimethylamino)naphthalene-2,7-diolate: a simple arylamine nitrogen base with hydride-ion-comparable proton affinity.

A. A. Milov, V. Minkin, A. F. Pozharskii, 2006, Angewandte Chemie.

peri-naphthylenediamines

A. F. Pozharskii, V. A. Ozeryanskii, A. M. Fomchenkov, 1998 .