ATOM-ECONOMIC SYNTHESIS OF NEW IMIDAZOLES AND BENZIMIDAZOLES WITH THIOPHOSPHORYL AND HYDROXYL GROUPS
DOI:
https://doi.org/10.1007/8344Keywords:
bis(2-phenylethyl)phosphine sulfide, 2-[bis(2-phenylethyl)thiophosphorylhydroxymethyl]-1-ethyl(vinyl)imidazoles, hydrochlorides of 2-[bis(2-phenylethyl)thiophosphorylhydroxymethyl]-1-ethyl(vinyl)imidazoles, 2-formyl-1-organylimidazoles, 2-formyl-1-organylbenzimidazoles, hydrothiophosphorylationAbstract
Nucleophilic addition of secondary phosphine sulfides to an aldehyde of the azole series occurs under noncatalytic conditions in THF at room temperature and enables the preparation in high yield of imidazoles and benzimidazoles with thiophosphoryl and hydroxyl groups, which are promising building blocks for organic synthesis and polydentate ligands for metal complexes.How to Cite
Ivanova, N. I.; Baikalova, L. V.; Konovalova, N. A.; Zyryanova, I. A.; Albanov, A. I.;
Sinegovskaya, L. M.; Kukhareva, V. A.; Tatarinova, A. A.; Avseenko, N. D.; Sukhov, B. G.; Gusarova, N. K.; Trofimov, B. A. Chem. Heterocycl. Compd. 2005, 41, 317. [Khim. Geterotsikl. Soedin. 2005, 365.]
For this article in the English edition, see DOI 10.1007/s10593-005-0150-3