Grygorenko OO - Search Results

1

Expanding the Chemical Space of 1,2-Difunctionalized Cyclobutanes.

Chernykh AV, Kudryk OV, Olifir OS, Dobrydnev AV, Rusanov E, Moskvina VS, Volochnyuk DM, Grygorenko OO. Chernykh AV, et al. Among authors: grygorenko oo. J Org Chem. 2023 Mar 3;88(5):3109-3131. doi: 10.1021/acs.joc.2c02892. Epub 2023 Feb 13. J Org Chem. 2023. PMID: 36780233

2

Approach to the library of fused pyridine-4-carboxylic acids by Combes-type reaction of acyl pyruvates and electron-rich amino heterocycles.

Volochnyuk DM, Ryabukhin SV, Plaskon AS, Dmytriv YV, Grygorenko OO, Mykhailiuk PK, Krotko DG, Pushechnikov A, Tolmachev AA. Volochnyuk DM, et al. Among authors: grygorenko oo. J Comb Chem. 2010 Jul 12;12(4):510-7. doi: 10.1021/cc100040q. J Comb Chem. 2010. PMID: 20459117

3

Cyclobutane-derived diamines: synthesis and molecular structure.

Radchenko DS, Pavlenko SO, Grygorenko OO, Volochnyuk DM, Shishkina SV, Shishkin OV, Komarov IV. Radchenko DS, et al. Among authors: grygorenko oo. J Org Chem. 2010 Sep 3;75(17):5941-52. doi: 10.1021/jo101271h. J Org Chem. 2010. PMID: 20695503

4

Bicyclic conformationally restricted diamines.

Grygorenko OO, Radchenko DS, Volochnyuk DM, Tolmachev AA, Komarov IV. Grygorenko OO, et al. Chem Rev. 2011 Sep 14;111(9):5506-68. doi: 10.1021/cr100352k. Epub 2011 Jun 28. Chem Rev. 2011. PMID: 21711015 No abstract available.

5

An entry into hexahydro-2H-thieno[2,3-c]pyrrole 1,1-dioxide derivatives.

Yarmolchuk VS, Mukan IL, Grygorenko OO, Tolmachev AA, Shishkina SV, Shishkin OV, Komarov IV. Yarmolchuk VS, et al. Among authors: grygorenko oo. J Org Chem. 2011 Sep 2;76(17):7010-6. doi: 10.1021/jo200878t. Epub 2011 Aug 9. J Org Chem. 2011. PMID: 21793557

6

1-Alkyl-5-((di)alkylamino) tetrazoles: building blocks for peptide surrogates.

Tymtsunik AV, Bilenko VA, Kokhan SO, Grygorenko OO, Volochnyuk DM, Komarov IV. Tymtsunik AV, et al. Among authors: grygorenko oo. J Org Chem. 2012 Jan 20;77(2):1174-80. doi: 10.1021/jo2022235. Epub 2011 Dec 30. J Org Chem. 2012. PMID: 22171684

7

Focused enumeration and assessing the structural diversity of scaffold libraries: conformationally restricted bicyclic secondary diamines.

Grygorenko OO, Prytulyak R, Volochnyuk DM, Kudrya V, Khavryuchenko OV, Komarov IV. Grygorenko OO, et al. Mol Divers. 2012 Aug;16(3):477-87. doi: 10.1007/s11030-012-9381-2. Epub 2012 Jul 3. Mol Divers. 2012. PMID: 22752707

8

Synthesis and structural analysis of angular monoprotected diamines based on spiro[3.3]heptane scaffold.

Chernykh AV, Radchenko DS, Grygorenko OO, Daniliuc CG, Volochnyuk DM, Komarov IV. Chernykh AV, et al. Among authors: grygorenko oo. J Org Chem. 2015 Apr 17;80(8):3974-81. doi: 10.1021/acs.joc.5b00323. Epub 2015 Mar 25. J Org Chem. 2015. PMID: 25768653

9

Beyond the Five and Six: Evaluation of Seven-Membered Cyclic Anhydrides in the Castagnoli-Cushman Reaction.

Adamovskyi MI, Ryabukhin SV, Sibgatulin DA, Rusanov E, Grygorenko OO. Adamovskyi MI, et al. Among authors: grygorenko oo. Org Lett. 2017 Jan 6;19(1):130-133. doi: 10.1021/acs.orglett.6b03426. Epub 2016 Dec 21. Org Lett. 2017. PMID: 28001424

10

Photochemical Synthesis of 3-Azabicyclo[3.2.0]heptanes: Advanced Building Blocks for Drug Discovery.

Denisenko AV, Druzhenko T, Skalenko Y, Samoilenko M, Grygorenko OO, Zozulya S, Mykhailiuk PK. Denisenko AV, et al. Among authors: grygorenko oo. J Org Chem. 2017 Sep 15;82(18):9627-9636. doi: 10.1021/acs.joc.7b01678. Epub 2017 Aug 25. J Org Chem. 2017. PMID: 28810741

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