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Non-natural 2H-azirine-2-carboxylic acids: an expedient synthesis and antimicrobial activity.
RSC Adv. 2019 Nov 21;9(65):37901-37905. doi: 10.1039/c9ra09345a. eCollection 2019 Nov 19.
RSC Adv. 2019.
PMID: 35541773
Free PMC article.
Azirine-containing dipeptides and depsipeptides: synthesis, transformations and antibacterial activity.
Rostovskii NV, Koronatov AN, Sakharov PA, Agafonova AV, Novikov MS, Khlebnikov AF, Rogacheva EV, Kraeva LA.
Rostovskii NV, et al. Among authors: koronatov an.
Org Biomol Chem. 2020 Dec 7;18(46):9448-9460. doi: 10.1039/d0ob02023k.
Org Biomol Chem. 2020.
PMID: 33170920
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Synthesis of 1,2-Dihydropyrimidine-2-carboxylates via Regioselective Addition of Rhodium(II) Carbenoids to 2H-Azirine-2-carbaldimines.
Novikov MS, Rostovskii NV, Koronatov AN, Zavyalov KV, Zubakin GV, Khlebnikov AF, Starova GL.
Novikov MS, et al. Among authors: koronatov an.
J Org Chem. 2017 Dec 15;82(24):13396-13404. doi: 10.1021/acs.joc.7b02484. Epub 2017 Nov 22.
J Org Chem. 2017.
PMID: 29131619
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Rh(II)-Catalyzed Ring Expansion of Pyrazoles with Diazocarbonyl Compounds as a Method for the Preparation of 1,2-Dihydropyrimidines.
Koronatov AN, Rostovskii NV, Khlebnikov AF, Novikov MS.
Koronatov AN, et al.
J Org Chem. 2018 Aug 17;83(16):9210-9219. doi: 10.1021/acs.joc.8b01228. Epub 2018 Jun 28.
J Org Chem. 2018.
PMID: 29916705
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Synthesis of 3-Alkoxy-4-Pyrrolin-2-ones via Rhodium(II)-Catalyzed Denitrogenative Transannulation of 1H-1,2,3-Triazoles with Diazo Esters.
Koronatov AN, Rostovskii NV, Khlebnikov AF, Novikov MS.
Koronatov AN, et al.
Org Lett. 2020 Oct 16;22(20):7958-7963. doi: 10.1021/acs.orglett.0c02893. Epub 2020 Oct 7.
Org Lett. 2020.
PMID: 33026817
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Rhodium-Catalyzed Denitrogenative Diazole-Triazole Coupling toward Aza-Bridged Structures and Imidazole-Based Chelating Ligands.
Strelnikova JO, Koronatov AN, Rostovskii NV, Khlebnikov AF, Khoroshilova OV, Kryukova MA, Novikov MS.
Strelnikova JO, et al. Among authors: koronatov an.
Org Lett. 2021 Jun 4;23(11):4173-4178. doi: 10.1021/acs.orglett.1c01092. Epub 2021 May 17.
Org Lett. 2021.
PMID: 33999636
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