7 article(s) from Dmitriev, Maksim V
Nucleophile-induced ring contraction in pyrrolo[2,1-c][1,4]benzothiazines: access to pyrrolo[2,1-b][1,3]benzothiazoles
- Ekaterina A. Lystsova,
- Maksim V. Dmitriev,
- Andrey N. Maslivets and
- Ekaterina E. Khramtsova
Beilstein J. Org. Chem. 2023, 19, 646–657, doi:10.3762/bjoc.19.46
A facile approach to spiro[dihydrofuran-2,3'-oxindoles] via formal [4 + 1] annulation reaction of fused 1H-pyrrole-2,3-diones with diazooxindoles
- Pavel A. Topanov,
- Anna A. Maslivets,
- Maksim V. Dmitriev,
- Irina V. Mashevskaya,
- Yurii V. Shklyaev and
- Andrey N. Maslivets
Beilstein J. Org. Chem. 2022, 18, 1532–1538, doi:10.3762/bjoc.18.162
Synthesis of 1,4-benzothiazinones from acylpyruvic acids or furan-2,3-diones and o-aminothiophenol
- Ekaterina E. Stepanova,
- Maksim V. Dmitriev and
- Andrey N. Maslivets
Beilstein J. Org. Chem. 2020, 16, 2322–2331, doi:10.3762/bjoc.16.193
Facile regiodivergent synthesis of spiro pyrrole-substituted pseudothiohydantoins and thiohydantoins via reaction of [e]-fused 1H-pyrrole-2,3-diones with thiourea
- Aleksandr I. Kobelev,
- Nikita A. Tretyakov,
- Ekaterina E. Stepanova,
- Maksim V. Dmitriev,
- Michael Rubin and
- Andrey N. Maslivets
Beilstein J. Org. Chem. 2019, 15, 2864–2871, doi:10.3762/bjoc.15.280
Annulation of 1H-pyrrole-2,3-diones by thioacetamide: an approach to 5-azaisatins
- Aleksandr I. Kobelev,
- Ekaterina E. Stepanova,
- Maksim V. Dmitriev and
- Andrey N. Maslivets
Beilstein J. Org. Chem. 2019, 15, 364–370, doi:10.3762/bjoc.15.32
Synthesis of pyrimido[1,6-a]quinoxalines via intermolecular trapping of thermally generated acyl(quinoxalin-2-yl)ketenes by Schiff bases
- Svetlana O. Kasatkina,
- Ekaterina E. Stepanova,
- Maksim V. Dmitriev,
- Ivan G. Mokrushin and
- Andrey N. Maslivets
Beilstein J. Org. Chem. 2018, 14, 1734–1742, doi:10.3762/bjoc.14.147
Regiodivergent condensation of 5-alkoxycarbonyl-1H-pyrrol-2,3-diones with cyclic ketazinones en route to spirocyclic scaffolds
- Alexey Yu. Dubovtsev,
- Maksim V. Dmitriev,
- Аndrey N. Maslivets and
- Michael Rubin
Beilstein J. Org. Chem. 2017, 13, 2179–2185, doi:10.3762/bjoc.13.218
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