Organic electrosynthesis | Edgars Suna Group

57. Entry to 2-aminoprolines via electrochemical decarboxylative amidation of N‑acetylamino malonic acid monoesters

Koleda O., Sadauskis J., Antonenko D., Treijs E. J., Steberis R. D., Suna E. Beilstein J. Org. Chem. 2025, 21, 630–638.
DOI: 10.3762/bjoc.21.50

47. Electrochemical Synthesis of Unnatural Amino Acids via Anodic Decarboxylation of N-Acetylamino Malonic Acid Derivatives

Koleda O., Prane K., Suna E. Org. Lett. 2023, 25 (44), 7958–7962.
DOI: https://doi.org/10.1021/acs.orglett.3c02687.

43. Electrochemical Synthesis of Dimeric λ3-Bromane: Platform for Hypervalent Bromine(III) Compounds

Sokolovs, I.; Suna, E.; Org. Lett. 2023, 25, 2047–2052. DOI: 10.1021/acs.orglett.3c00405

42. Simple and scalable electrosynthesis of 1H-1-hydroxy-quinazolin-4-ones

Koleda, O.; Prenzel, T,; Winter, J.; Hirohata, T.; Gálvez-Vázquez, J.; Schollmeyer, D.; Inagi, S.; Suna, E.; Waldvogel, S. R.; Chem. Sci. 2023, 14, 2669-2675. DOI: 10.1039/D3SC00266G

40. Electrochemistry and Reactivity of Chelation-stabilized Hypervalent Bromine(III) Compounds

Mohebbati, N.; Sokolovs, i.; Woite, P.; Lõkov, M.; Parman, E.; Ugandi, M.; Leito, I.; Roemelt, M.; Suna, E.; Francke, R.; Chem-Eur. J. 2022, 28, e202200974.

DOI: 10.1002/chem.202200974

34. Electrochemical Generation of Hypervalent Bromine(III) Compounds

Sokolovs, I.; Mohebbati, N.; Francke, R.; Suna, E. Angew. Chem. Int. Ed. 2021, 60, 15832–15837. Download publication.

DOI: 10.1002/anie.202104677

26. Simple and scalable electrochemical synthesis of 2,1-benzisoxazoles and quinoline N-oxides

Rodrigo, E.; Baunis, H.; Suna, E.; Waldvogel, S., R. Chem. Commun., 2019, 55, 12255-1225.

DOI: 10.1039/C9CC06054E

19. Synthesis of Benzoxazoles Using Electrochemically Generated Hypervalent Iodine

Koleda, O.; Broese, T.; Noetzel, J.; Roemelt, M.; Suna, E.; Francke, R. J. Org. Chem. 2017, 82, 11669–11681.

DOI: 10.1021/acs.joc.7b01686

Category "Organic electrosynthesis"