Новости События Общее

Publications

31-05-2020 Publications
Papers in chronological order

2020

V. Kovalenko,* N. Tumanov, K. Vasiutovich, T. Leyssens. Ethoxycarbonyl functionalized Tröger’s base alongside its congener dihydroquinazoline: a trick with crystallization. Chemical Data Collections 2020, 25, 100339, https://doi.org/10.1016/j.cdc.2020.100339

 

2019

V. Kovalenko,* K. Vasiutovich. Scalable synthesis of N-acetylated α-amino acid derived oxazoline ligands. J. Heterocyclic Chem. 2019, 56, 909–914, https://doi.org/10.1002/jhet.3468

 

T.-H. Jeon, H.-J. Kang, A. Svirid, A. Lyakhov, V. Kovalenko,* C.-G. Cho.* Chiral resolution of racemic 2-pyrone Diels-Alder cycloadduct by diastereomeric salt formation. Bull. Korean Chem. Soc. 2019, 40, 910–913, https://doi.org/10.1002/bkcs.11838

 

V. Kovalenko,* A. Krauchanka, K. Prokhorevich.Practical method for increasing optical purity of cis-verbenol. Chirality 2019, 31, 865–869, https://doi.org/10.1002/chir.23119

 
 
2017
 
V.N. Kovalenko,* A.S. Prat’ko, K.N. Prokhorevich. Crystallization of bisulfite derivatives of enantiomerically enriched verbenone. Russ. J. Org. Chem. 2017, 53, 1598–1600, https://doi.org/10.1134/S1070428017100190
 
 
V.N. Kovalenko,* А.S. Pratsko. Selective hydrogenation of conjugated unsaturated ketones containing a hydroxyaryl substituent in the β-position. Russ. J. Org. Chem. 2017, 53, 24–28, http://dx.doi.org/10.1134/S1070428017010055
 
 
2016
 
V.N. Kovalenko,* K.N. Pokchorevich. Improved synthesis of optically active ipsdienol. Russ. J. Org. Chem. 2016, 52, 757–758,
 
 
2015
 
V.N. Kovalenko,* Yu.Yu. Kozyrkov. A simple method for resolution of endo-/exo-monoesters of trans-norborn-5-ene-2,3-dicarboxylic acids into their enantiomers. Chirality 2015, 27, 151–155, http://dx.doi.org/10.1002/chir.22404
 
 
2014
 
V.N. Kovalenko. Chiral methyl trans-2,2-dichloro-3-methylcyclopropanecarboxylate upon exposure to thiophenolate nucleophile. Arkivoc 2014 (iii), 80–89, http://dx.doi.org/10.3998/ark.5550190.p008.380
 
 
M. Bandarenko, V. Kovalenko.* Synthesis of raspberry and ginger ketones by nickel boride-catalyzed hydrogenation of 4-arylbut-3-en-2-ones. Zeitschrift für Naturforschung B 2014, 69b, 885–888, http://dx.doi.org/10.5560/ZNB.2014-4118
 
 

I.V. Mineeva, V.S. Masyuk, V.N. Kovalenko, M.M. Bandarenko. (4S,6R)-4-methyl-6-pentyltetrahydro-2H-pyran-2-one as an efficient intermediate in the preparation of chiral building blocks with methyl-branched carbon skeleton. Application to the synthesis of bioactive compounds. Russ. J. Org. Chem. 2014, 50, 1621–1627. https://doi.org/10.1134/S1070428014110141

 

V.N. Kovalenko, I.V. Mineeva. Cyclopropane intermediates in the synthesis of chiral alcohols with methyl-branched carbon skeleton. Application in the synthesis of insect pheromones. Russ. J. Org. Chem. 2014, 50, 934–942. https://doi.org/10.1134/S1070428014070033
 
 
2012
 
V. Kovalenko,* E. Matiushenkov. Stereoselective synthesis of (2S,3S,7S)-3,7-dimethylpentadecan-2-ol and its propionate, the sex pheromones of pine sawflies. Tetrahedron: Asymmetry 2012, 23, 1393–1399, http://dx.doi.org/10.1016/j.tetasy.2012.09.002
 
 
V.N. Kovalenko, E.A. Matiushenkov. Stereoselective synthesis of (R)- and (S)-ipsdienols, pheromone components of bark beetles of the Ips family. Russ. J. Org. Chem. 2012, 48, 1168–1172, http://dx.doi.org/10.1134/S1070428012090035
 
 
2011
 
V.N. Kovalenko, O.G. Kulinkovich. The resolution of trans-2,2-dichloro-3-methylcyclopropanecarboxylic acid via crystallization of its salts with (+)- and (–)-α-phenylethylamine, and the transformation of the resulting enantiomers into (R)- and (S)-dimethyl 2‑methylsuccinates. Tetrahedron: Asymmetry 2011, 22, 26–30, http://dx.doi.org/10.1016/j.tetasy.2010.12.014
 
 
2010
 

V.N. Kovalenko, N.A. Sokolov, O.G. Kulinkovich. Synthesis of epothilones molecule fragment (15R)-C13-C21 from D-mannitol. Russ. J. Org. Chem. 2010, 46, 1702–1708, https://doi.org/10.1134/S1070428010110175

 

2009

V.N. Kovalenko, N.V. Masalov, O.G. Kulinkovich. Synthesis of (+)-disparlure from diethyl (−)-malate via opening and fragmentation of the three-membered ring in tertiary cyclopropanols. Russ. J. Org. Chem. 2009, 45, 1318–1324, https://doi.org/10.1134/S1070428009090036

 

Unpublished

1. V. Kovalenko. A new protocol for reductive aldol coupling between vinyl ketones and aldehydes. Conference GDCh 150: Wissenschaftsforum Chemie, September 2017, Berlin. Poster ORG 035

 

2. V. Kovalenko. Self-cleaving N-aryl amides: solvent and temperature dependent equilibrium. Virtual Systems Chemistry Symposium, May 2020. Twitter poster

 

 

 

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