Synthesis of imidazo[1,2-a]pyridine-containing peptidomimetics by tandem of Groebke–Blackburn–Bienaymé and Ugi reactions

Oleksandr V. Kolomiiets, Alexander V. Tsygankov, Maryna N. Kornet, Aleksander A. Brazhko, Vladimir I. Musatov and Valentyn A. Chebanov
Beilstein J. Org. Chem. 2023, 19, 727–735. https://doi.org/10.3762/bjoc.19.53

Supporting Information

Supporting Information File 1: Experimental part.
Format: PDF Size: 6.8 MB Download

Cite the Following Article

Synthesis of imidazo[1,2-a]pyridine-containing peptidomimetics by tandem of Groebke–Blackburn–Bienaymé and Ugi reactions
Oleksandr V. Kolomiiets, Alexander V. Tsygankov, Maryna N. Kornet, Aleksander A. Brazhko, Vladimir I. Musatov and Valentyn A. Chebanov
Beilstein J. Org. Chem. 2023, 19, 727–735. https://doi.org/10.3762/bjoc.19.53

How to Cite

Kolomiiets, O. V.; Tsygankov, A. V.; Kornet, M. N.; Brazhko, A. A.; Musatov, V. I.; Chebanov, V. A. Beilstein J. Org. Chem. 2023, 19, 727–735. doi:10.3762/bjoc.19.53

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: 9.6 MB Download

Citations to This Article

Up to 20 of the most recent references are displayed here.

Scholarly Works

  • Zorigt, N.; Zarei, A.; Auras, F.; Khazdooz, L.; Khosropour, A.; Abbaspourrad, A. Synthesis of Homoallylamine Covalent Organic Frameworks Via Hosomi-Sakurai Reaction Under Mild Conditions. Small (Weinheim an der Bergstrasse, Germany) 2024, e2406805. doi:10.1002/smll.202406805
  • Martini, C.; Mardjan, M. I. D.; Basso, A. The Groebke-Blackburn-Bienaymé reaction in its maturity: innovation and improvements since its 21st birthday (2019-2023). Beilstein journal of organic chemistry 2024, 20, 1839–1879. doi:10.3762/bjoc.20.162
  • Tsygankov, A. V.; Vereshchak, V. O.; Savluk, T. O.; Desenko, S. M.; Ananieva, V. V.; Buravov, O. V.; Sakhno, Y. I.; Shishkina, S. V.; Chebanov, V. A. Ugi bisamides based on pyrrolyl-β-chlorovinylaldehyde and their unusual transformations. Beilstein journal of organic chemistry 2024, 20, 1773–1784. doi:10.3762/bjoc.20.156
  • Govor, E. V.; Naumchyk, V.; Nestorak, I.; Radchenko, D. S.; Dudenko, D.; Moroz, Y. S.; Kachkovsky, O. D.; Grygorenko, O. O. Generation of multimillion chemical space based on the parallel Groebke-Blackburn-Bienaymé reaction. Beilstein journal of organic chemistry 2024, 20, 1604–1613. doi:10.3762/bjoc.20.143
  • Murlykina, M.; Pavlovska, T.; Semenenko, O.; Kolomiets, O.; Sanin, E.; Morozova, A.; Kornet, M.; Musatov, V.; Kulyk, K.; Mazepa, A.; Lipson, V.; Chebanov, V. Effective Three‐Step Construction of Betulonic Acid Hybrids with Heterocycle‐Containing Peptidomimetic Fragments. ChemistrySelect 2023, 8. doi:10.1002/slct.202301250
Other Beilstein-Institut Open Science Activities