Collect. Czech. Chem. Commun.
1979, 44, 1475-1482
https://doi.org/10.1135/cccc19791475
Synthetic use of the ribosyl derivatives of 2,4- and 2,5-thiazolidinediones
Hubert Hřebabecký, Zdeněk Točík and Jiří Beránek
Institute of Organic Chemistry and Biochemistry, Czechoslovak Academy of Sciences, 166 10 Prague 6
Crossref Cited-by Linking
- Zhong Yong-Li, Ji Yining, Wang Heather, Wang Xiao, Gauthier Donald R.: Highly Enantioselective Rhodium-Catalyzed Transfer Hydrogenation of Tetrasubstituted Olefins: Application toward the Synthesis of GPR40 Agonist MK-2305. Org. Lett. 2022, 24, 3254. <https://doi.org/10.1021/acs.orglett.2c01021>
- Zsila Ferenc: Comment on “Multiple Independent Binding Sites for Small-Molecule Inhibitors on the Oncoprotein c-Myc”. J. Phys. Chem. B 2016, 120, 10611. <https://doi.org/10.1021/acs.jpcb.6b08431>
- Metwally M. A., Etman H. A., Keshk E. M., Fekry A.: Thiazolidin-5-Ones: Synthesis and Reactions. Phosphorus, Sulfur, and Silicon and the Related Elements 2006, 181, 1039. <https://doi.org/10.1080/10426500500326263>
- Fedoseeva N. M., Zavadskaya M. I., Kvasyuk E. I., Drachenova O. A., Boreko E. I.: 5-Arylidene derivatives of 3-β-D-ribofuranosylthiazolidine-2,4-dione. Chem Heterocycl Compd 1983, 19, 740. <https://doi.org/10.1007/BF00506098>
- HREBABECKY H., TOCIK Z., BERANEK J.: ChemInform Abstract: ANALOGS OF NUCLEOSIDES. XVIII. SYNTHETIC USE OF THE RIBOSYL DERIVATIVES OF 2,4‐ AND 2,5‐THIAZOLIDINEDIONES. Chemischer Informationsdienst 1979, 10. <https://doi.org/10.1002/chin.197935332>