Victor I Mamatyuk
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Explore the profile of Victor I Mamatyuk including associated specialties, affiliations and a list of published articles.
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5
Citations
23
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Recent Articles
1.
Vasilevsky S, Baranov D, Mamatyuk V, Fadeev D, Gatilov Y, Stepanov A, et al.
J Org Chem
. 2015 Jan;
80(3):1618-31.
PMID: 25575160
Reductive dimerization of acetylenic anthraquinones provides synthetic access to flexible nonplanar polyaromatics with a tetracenedione core. In solution, these nonplanar, contorted polycycles exist as equilibrating mixtures of two symmetric conformers....
2.
Tormyshev V, Genaev A, Salnikov G, Rogozhnikova O, Troitskaya T, Trukhin D, et al.
European J Org Chem
. 2013 Dec;
2012(3).
PMID: 24294110
Triarylmethanols - the direct precursors of persistent trityl radicals - are racemic mixtures of chiral three-bladed molecular propellers. Depending on bulkiness of aryl groups they exhibit various liabilities to interconversion,...
3.
Yanshole V, Sherin P, Gritsan N, Snytnikova O, Mamatyuk V, Grilj J, et al.
Phys Chem Chem Phys
. 2010 Jul;
12(32):9502-15.
PMID: 20617247
The properties of xanthurenic acid (XAN) in ground and photoexcited states have been studied using steady-state and time-resolved optical methods as well as quantum chemistry calculations. In neutral aqueous solution...
4.
Vasilevsky S, Mikhailovskaya T, Mamatyuk V, Salnikov G, Bogdanchikov G, Manoharan M, et al.
J Org Chem
. 2009 Sep;
74(21):8106-17.
PMID: 19780573
Depending on the reaction conditions and the nature of substituents at the triple bond, anionic cyclizations of hydrazides of o-acetylenyl benzoic acids can be selectively directed along three alternative paths,...
5.
Vasilevsky S, Baranov D, Mamatyuk V, Gatilov Y, Alabugin I
J Org Chem
. 2009 Jul;
74(16):6143-50.
PMID: 19585968
This work analyzes multiple new reaction pathways which originate from intramolecular reactions of activated alkynes with the appropriately positioned multifunctional hemiaminal moiety. Combination of experimental substituent effects with Natural Bond...