Alabugin IV - Search Results

1

Conformational flexibility of fused tetracenedione propellers obtained from one-pot reductive dimerization of acetylenic quinones.

Vasilevsky SF, Baranov DS, Mamatyuk VI, Fadeev DS, Gatilov YV, Stepanov AA, Vasilieva NV, Alabugin IV. Vasilevsky SF, et al. Among authors: alabugin iv. J Org Chem. 2015 Feb 6;80(3):1618-31. doi: 10.1021/jo502543b. Epub 2015 Jan 27. J Org Chem. 2015. PMID: 25575160

2

Design and Synthesis of Kekulè and Non-Kekulè Diradicaloids via the Radical Periannulation Strategy: The Power of Seven Clar's Sextets.

Kuriakose F, Commodore M, Hu C, Fabiano CJ, Sen D, Li RR, Bisht S, Üngör Ö, Lin X, Strouse GF, DePrince AE 3rd, Lazenby RA, Mentink-Vigier F, Shatruk M, Alabugin IV. Kuriakose F, et al. Among authors: alabugin iv. J Am Chem Soc. 2022 Dec 28;144(51):23448-23464. doi: 10.1021/jacs.2c09637. Epub 2022 Dec 14. J Am Chem Soc. 2022. PMID: 36516873

3

Anticancer and Antiphytopathogenic Activity of Fluorinated Isatins and Their Water-Soluble Hydrazone Derivatives.

Bogdanov AV, Neganova M, Voloshina A, Lyubina A, Amerhanova S, Litvinov IA, Tsivileva O, Akylbekov N, Zhapparbergenov R, Valiullina Z, Samorodov AV, Alabugin I. Bogdanov AV, et al. Int J Mol Sci. 2023 Oct 12;24(20):15119. doi: 10.3390/ijms242015119. Int J Mol Sci. 2023. PMID: 37894799 Free PMC article.

4

Photochemical Uncaging of Aldehydes and Ketones via Photocyclization/Fragmentation Cascades of Enyne Alcohols: An Unusual Application for a Cycloaromatization Process.

Campbell A, Dos Santos NR, Alabugin I. Campbell A, et al. Molecules. 2023 Jul 28;28(15):5704. doi: 10.3390/molecules28155704. Molecules. 2023. PMID: 37570675 Free PMC article.

5

α-Methylstilbene Isomers: Relationship of Structure to Photophysics and Photochemistry.

Krishnan SB, Clark RJ, Lin X, Dmitrenko O, Hilinski EF, Kuhn LR, Alabugin IV, Saltiel J. Krishnan SB, et al. Among authors: alabugin iv. J Phys Chem A. 2022 Dec 8;126(48):8976-8987. doi: 10.1021/acs.jpca.2c06319. Epub 2022 Nov 22. J Phys Chem A. 2022. PMID: 36414392

6

An unexpected rearrangement that disassembles alkyne moiety through formal nitrogen atom insertion between two acetylenic carbons and related cascade transformations: new approach to Sampangine derivatives and polycyclic aromatic amides.

Vasilevsky SF, Baranov DS, Mamatyuk VI, Gatilov YV, Alabugin IV. Vasilevsky SF, et al. Among authors: alabugin iv. J Org Chem. 2009 Aug 21;74(16):6143-50. doi: 10.1021/jo9008904. J Org Chem. 2009. PMID: 19585968

7

Tuning selectivity of anionic cyclizations: competition between 5-exo and 6-endo-dig closures of hydrazides of o-acetylenyl benzoic acids and based-catalyzed fragmentation/recyclization of the initial 5-exo-dig products.

Vasilevsky SF, Mikhailovskaya TF, Mamatyuk VI, Salnikov GE, Bogdanchikov GA, Manoharan M, Alabugin IV. Vasilevsky SF, et al. Among authors: alabugin iv. J Org Chem. 2009 Nov 6;74(21):8106-17. doi: 10.1021/jo901551g. J Org Chem. 2009. PMID: 19780573

8

Dissecting alkynes: full cleavage of polarized C≡C moiety via sequential bis-Michael addition/retro-Mannich cascade.

Roy S, Davydova MP, Pal R, Gilmore K, Tolstikov GA, Vasilevsky SF, Alabugin IV. Roy S, et al. Among authors: alabugin iv. J Org Chem. 2011 Sep 16;76(18):7482-90. doi: 10.1021/jo201259j. Epub 2011 Aug 19. J Org Chem. 2011. PMID: 21806030

9

Chameleonic reactivity of vicinal diazonium salt of acetylenyl-9,10-anthraquinones: synthetic application toward two heterocyclic targets.

Stepanov AA, Gornostaev LM, Vasilevsky SF, Arnold EV, Mamatyuk VI, Fadeev DS, Gold B, Alabugin IV. Stepanov AA, et al. Among authors: alabugin iv. J Org Chem. 2011 Nov 4;76(21):8737-48. doi: 10.1021/jo2014214. Epub 2011 Oct 4. J Org Chem. 2011. PMID: 21910478

10

Divergent cyclizations of 1-R-ethynyl-9,10-anthraquinones: use of thiourea as a "S2-" equivalent in an "anchor-relay" addition mediated by formal C-H activation.

Baranov DS, Gold B, Vasilevsky SF, Alabugin IV. Baranov DS, et al. Among authors: alabugin iv. J Org Chem. 2013 Mar 1;78(5):2074-82. doi: 10.1021/jo302146r. Epub 2012 Dec 4. J Org Chem. 2013. PMID: 23163879

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