Supporting Information
| Supporting Information File 1: Experimental details, copies of 1H and 13C NMR spectra of pyrimido[1,6-a]quinoxalines 3a–n, STA plots of PQT 1a–h and X-ray crystal structure details of compounds 3g,j. | ||
| Format: PDF | Size: 2.5 MB | Download |
Cite the Following Article
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.
https://doi.org/10.3762/bjoc.14.147
How to Cite
Kasatkina, S. O.; Stepanova, E. E.; Dmitriev, M. V.; Mokrushin, I. G.; Maslivets, A. N. Beilstein J. Org. Chem. 2018, 14, 1734–1742. doi:10.3762/bjoc.14.147
Download Citation
Citation data can be downloaded as file using the "Download" button or used for copy/paste from the text window
below.
Citation data in RIS format can be imported by all major citation management software, including EndNote,
ProCite, RefWorks, and Zotero.
Presentation Graphic
| Picture with graphical abstract, title and authors for social media postings and presentations. | ||
| Format: PNG | Size: 172.6 KB | Download |
Citations to This Article
Up to 20 of the most recent references are displayed here.
Scholarly Works
- Topanov, P. A.; Maslivets, A. A.; Dmitriev, M. V.; Mashevskaya, I. V.; Shklyaev, Y. V.; Maslivets, A. N. A facile approach to spiro[dihydrofuran-2,3'-oxindoles] via formal [4 + 1] annulation reaction of fused 1H-pyrrole-2,3-diones with diazooxindoles. Beilstein journal of organic chemistry 2022, 18, 1532–1538. doi:10.3762/bjoc.18.162
- Khramtsova, E. E.; Krainov, A. D.; Dmitriev, M. V.; Maslivets, A. N. Cycloaddition of 4-Acyl-1H-pyrrole-2,3-diones Fused at [e]-Side and Cyanamides: Divergent Approach to 4H-1,3-Oxazines. Molecules (Basel, Switzerland) 2022, 27, 5257. doi:10.3390/molecules27165257
- Lystsova, E. A.; Khramtsova, E. E.; Maslivets, A. N. Acyl(imidoyl)ketenes: Reactive Bidentate Oxa/Aza-Dienes for Organic Synthesis. Symmetry 2021, 13, 1509. doi:10.3390/sym13081509
- Moroz, A. A.; Zhulanov, V. E.; Dmitriev, M. V.; Maslivets, A. N. Diversity-oriented synthesis of three skeletally diverse iminolactones from isocyanides, activated acetylenes and 1H-pyrrole-2,3-diones via [3+2] and [4+1] cycloaddition reactions. Tetrahedron 2020, 76, 130880. doi:10.1016/j.tet.2019.130880
- Zhang, Y.; Li, H.; Jiang, D.; Pu, S. A highly selective fluorescent chemosensor for Mg 2+ based on a diarylethene with a quinoxaline unit. Journal of Physical Organic Chemistry 2019, 33, 4030. doi:10.1002/poc.4030
- Kasatkina, S. O.; Stepanova, E. E.; Dmitriev, M. V.; Mokrushin, I. G.; Maslivets, A. N. Divergent synthesis of (quinoxalin-2-yl)-1,3-oxazines and pyrimido[1,6-a]quinoxalines via the cycloaddition reaction of acyl(quinoxalinyl)ketenes. Tetrahedron Letters 2019, 60, 151088. doi:10.1016/j.tetlet.2019.151088