This microreview is dedicated to new and modified existing methods for the formation of the 1,3-oxazolidin-2-one ring. The material covers key studies published since 2021.
Similar content being viewed by others
References
(a) Yuan, L.; Sheng, R.; Guan, M.; Wang, Y.; Chen, S. Curr. Med. Chem. 2023, 30, 2672. (b) Jadhavar, P. S.; Vaja, M. D.; Dhameliya, T. M.; Chakraborti, A. K. Curr. Med. Chem. 2015, 22, 4379.
Yuan, S.; Shen, D.-D.; Bai, Y.-R.; Zhang, M.; Zhou, T.; Sun, C.; Zhou, L.; Wang, S.-Q.; Liu, H.-M. Eur. J. Med. Chem. 2023, 250, 115239.
(a) Wang, B.-L.; Guo, Z.-Q.; Wei, X.-H. J. Fuel Chem. Technol. 2023, 51, 85. (b) Sun, F.; Van der Eycken, E. V.; Feng, H. Adv. Synth. Catal. 2021, 363, 5168. (c) Okuno, K.; Nishiyori, R.; Abe, K.; Mori, T.; Shirakawa, S. Chirality 2022, 34, 915.
Kitamura, Y.; Ohshima, Y.; Nagaya, Y. Tetrahedron Lett. 2022, 88, 153554.
Yoshida, Y.; Endo, T. Tetrahedron Lett. 2021, 72, 153086.
Choi, H.; Jang, H.; Choi, J.; Lee, K. Molecules 2021, 26, 597.
Das, M.; Rodríguez, A.; Lo, P. K. T.; Moran, W. J. Adv. Synth. Catal. 2021, 363, 1646.
(a) Kim, J.; Lee, D. H.; Kim, J. Adv. Synth. Catal. 2021, 363, 4728. (b) Papa Spadafora, B.; Moreira Ribeiro, F. W.; Matsushima, J. E.; Miho Ariga, E.; Omari, I.; Machado Arruda Soares, P.; de Oliveira-Silva, D.; Vinhato, E.; McIndoe, J. S.; Carita Correra, T.; Rodrigues, A. Org. Biomol. Chem. 2021, 19, 5595. (c) McNichol, C. P.; DeCicco, E. M.; Canfield, A. M.; Carstairs, D. P.; Paradine, S. M. ACS Catal. 2023, 13, 6568.
Tu, J.-L.; Yang, J.-W.; Xu, W.; Su, M.; Liu, F. Org. Chem. Front. 2021, 8, 6405.
Giofrè, S.; Loro, C.; Molteni, L.; Castellano, C.; Contini, A.; Nava, D.; Broggini G.; Beccalli, E. M. Eur. J. Org. Chem. 2021, 1750.
Nishiyori, R.; Mori, T.; Shirakawa, S. Org. Biomol. Chem. 2023, 21, 4002.
(a) Nayak, P.; Chandrasekar Murali, A.; Rao Velpuri, V.; Chandrasekhar, V.; Venkatasubbaiah, K. Adv. Synth. Catal. 2023, 365, 230. (b) Cavalleri, M.; Damiano, C.; Manca, G.; Gallo, E. Chem.– Eur. J. 2023, 29, e202202729.
Xie, Y.; Feng, H.; Qi, Y.; Huang, J.; Huang, L. J. Org. Chem. 2021, 86, 16940.
Mandal, P. S.; Vijay Kumar, A. Asian J. Org. Chem. 2022, 11, e202100735.
Wata, C.; Hashimoto, T. J. Am. Chem. Soc. 2021, 143, 1745.
Fehr, L.; Sewald, L.; Huber, R.; Kaiser, M. Eur. J. Org. Chem. 2023, 26, e202300135.
Zhou, C.; Chen, X.; Lv, T.; Han, X.; Feng, J.; Liu, W.; Wu Q.; Zhu, D. ACS Catal. 2023, 13, 4768.
Author information
Authors and Affiliations
Corresponding author
Additional information
Translated from Khimiya Geterotsiklicheskikh Soedinenii, 2023, 59(11/12), 733–735
Rights and permissions
Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
About this article
Cite this article
Litvinova, V.A., Tikhomirov, A.S. Methods for the synthesis of 1,3-oxazolidin-2-ones (microreview). Chem Heterocycl Comp 59, 733–735 (2023). https://doi.org/10.1007/s10593-024-03263-w
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s10593-024-03263-w