Alexey M Starosotnikov
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Explore the profile of Alexey M Starosotnikov including associated specialties, affiliations and a list of published articles.
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8
Citations
6
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Recent Articles
1.
Nikolskiy V, Minyaev M, Bastrakov M, Starosotnikov A
Beilstein J Org Chem
. 2024 May;
20:1069-1075.
PMID: 38774274
An efficient method for the synthesis of isoxazolo[4,5-]pyridines has been developed on the basis of readily available 2-chloro-3-nitropyridines via the intramolecular nucleophilic substitution of the nitro group as a key...
2.
Starosotnikov A, Bastrakov M
Int J Mol Sci
. 2023 Jun;
24(11).
PMID: 37298265
Human immunodeficiency virus (HIV) causes one of the most dangerous diseases-acquired immunodeficiency syndrome (AIDS). An estimated about 40 million people are currently living with HIV worldwide, most of whom are...
3.
Melnikov I, Kiselev V, Dalinger I, Starosotnikov A, Muravyev N, Pivkina A
Int J Mol Sci
. 2023 Mar;
24(6).
PMID: 36982405
Nitro derivatives of benzotriazoles are safe energetic materials with remarkable thermal stability. In the present study, we report on the kinetics and mechanism of thermal decomposition for 5,7-dinitrobenzotriazole () and...
4.
Nikolskiy V, Minyaev M, Bastrakov M, Starosotnikov A
Int J Mol Sci
. 2023 Jan;
24(2).
PMID: 36675281
An efficient method for the synthesis of pyrazolo [4,3-]pyridines has been developed on the basis of readily available 2-chloro-3-nitropyridines via a sequence of SNAr and modified Japp-Klingemann reactions. The method...
5.
Nikolskiy V, Minyaev M, Bastrakov M, Starosotnikov A
Molecules
. 2022 Sep;
27(17).
PMID: 36080461
A number of new 2-methyl- and 2-arylvinyl-3-nitropyridines were synthesized and their reactions with thiols were studied. It was found that 3-NO tends to be selectively substituted under the action of...
6.
Bastrakov M, Fedorenko A, Starosotnikov A, Shakhnes A
Molecules
. 2021 Sep;
26(18).
PMID: 34577019
1,3-Dipolar cycloaddition reactions of 2-substituted 5--3-nitropyridines and isomeric 3--5-nitropyridines with N-methyl azomethine ylide were studied. The effect of the substituent at positions 2 and 5 of the pyridine ring on...
7.
Bastrakov M, Fedorenko A, Starosotnikov A, Fedyanin I, Kokorekin V
Molecules
. 2020 May;
25(9).
PMID: 32397095
A number of novel 6-R-isoxazolo[4,3-]pyridines were synthesized and their reactions with neutral C-nucleophiles (1,3-dicarbonyl compounds, π-excessive (het)arenes, dienes) were studied. The reaction rate was found to be dependent on the...
8.
Starosotnikov A, Shkaev D, Bastrakov M, Fedyanin I, Shevelev S, Dalinger I
Beilstein J Org Chem
. 2018 Mar;
13:2854-2861.
PMID: 29564013
4-Aza-6-nitrobenzofuroxan (ANBF) reacts with 1,3-dicarbonyl compounds and other CH acids to give carbon-bonded 1,4-adducts - 1,4-dihydropyridines fused with furoxan ring. In the case of most acidic β-diketones, which exist mainly...