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Page 1
Thioisomünchnones versus Acrylamides via Copper-Catalyzed Reaction of Thioamides with Diazocarbonyl Compounds.
J Org Chem. 2022 Sep 16;87(18):12196-12213. doi: 10.1021/acs.joc.2c01352. Epub 2022 Aug 25.
J Org Chem. 2022.
PMID: 36007261
Cycloaddition reactions of heterocyclic azides with 2-cyanoacetamidines as a new route to C,N-diheteroarylcarbamidines.
Silaichev PS, Beryozkina TV, Melekhin VV, Filimonov VO, Maslivets AN, Ilkin VG, Dehaen W, Bakulev VA.
Silaichev PS, et al. Among authors: filimonov vo.
Beilstein J Org Chem. 2024 Jan 5;20:17-24. doi: 10.3762/bjoc.20.3. eCollection 2024.
Beilstein J Org Chem. 2024.
PMID: 38213842
Free PMC article.
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Cyanothioacetamides as a synthetic platform for the synthesis of aminopyrazole derivatives.
Filimonov VO, Topchiy AI, Ilkin VG, Beryozkina TV, Bakulev VA.
Filimonov VO, et al.
Beilstein J Org Chem. 2023 Aug 8;19:1191-1197. doi: 10.3762/bjoc.19.87. eCollection 2023.
Beilstein J Org Chem. 2023.
PMID: 37592935
Free PMC article.
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Spiroheterocyclization of methyl 1-aryl-3-cinnamoyl-4,5-dioxo-4,5-dihydro-1H-pyrrole-2-carboxylates by the action of 3-(arylamino)-1H-inden-1-ones.
Silaichev PS, Filimonov VO, Slepukhin PA, Maslivets AN.
Silaichev PS, et al. Among authors: filimonov vo.
Molecules. 2012 Nov 22;17(12):13787-94. doi: 10.3390/molecules171213787.
Molecules. 2012.
PMID: 23174896
Free PMC article.
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Water/Alkali-Catalyzed Reactions of Azides with 2-Cyanothioacetamides. Eco-Friendly Synthesis of Monocyclic and Bicyclic 1,2,3-Thiadiazole-4-carbimidamides and 5-Amino-1,2,3-triazole-4-carbothioamides.
Filimonov VO, Dianova LN, Beryozkina TV, Mazur D, Beliaev NA, Volkova NN, Ilkin VG, Dehaen W, Lebedev AT, Bakulev VA.
Filimonov VO, et al.
J Org Chem. 2019 Nov 1;84(21):13430-13446. doi: 10.1021/acs.joc.9b01599. Epub 2019 Oct 4.
J Org Chem. 2019.
PMID: 31547663
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Switchable Synthesis of 4,5-Functionalized 1,2,3-Thiadiazoles and 1,2,3-Triazoles from 2-Cyanothioacetamides under Diazo Group Transfer Conditions.
Filimonov VO, Dianova LN, Galata KA, Beryozkina TV, Novikov MS, Berseneva VS, Eltsov OS, Lebedev AT, Slepukhin PA, Bakulev VA.
Filimonov VO, et al.
J Org Chem. 2017 Apr 21;82(8):4056-4071. doi: 10.1021/acs.joc.6b02736. Epub 2017 Apr 3.
J Org Chem. 2017.
PMID: 28328204
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