Аннотация:
The synthesis of the first co-crystals among 4,5-dihydroxy-4,5-diphenylimidazolidin-2-ones (4,5-dihydroxyimidazolidine- 2-thione + 5-hydroxy-4-methoxy-4,5-diphenyl-1,3-diethylimidazolidine-2-thione) and of the cis isomer of 1,3-diethyl-4,5-dihydroxy- 4,5-diphenylimidazolidine-2-thione through the regiospecific condensation of 1,3-diethylthiourea with 1,2-dioxo-1,2-diphenylethane was implemented; the structure was ascertained by single crystal X-ray diffraction and X-ray phase analysis.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
V. V. Baranov, Yu. V. Nelyubina, A. A. Korlyukov, A. N. Kravchenko, “Co-crystals in the series of 4,5-dihydroxy- 4,5-diphenylimidazolidine-2-thiones”, Mendeleev Commun., 19:4 (2009), 211–213
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc3173
https://www.mathnet.ru/rus/mendc/v19/i4/p211
Эта публикация цитируется в следующих 8 статьяx:
Soumitra Rana, Soumyadip Basu, Chhanda Mukhopadhyay, “An environment-friendly methodology for the construction of diversified bicycloacenaphtho[1,2-d]imidazole-8-thione scaffolds using spinel NiFe2O4 nanoparticles as a sustainable catalyst”, Mol Divers, 26:5 (2022), 2561
Н. Н. Махова, Л. И. Беленький, Г. А. Газиева, И. Л. Далингер, Л. С. Константинова, В. В. Кузнецов, А. Н. Кравченко, М. М. Краюшкин, О. А. Ракитин, А. М. Старосотников, Л. Л. Ферштат, С. А. Шевелев, В. З. Ширинян, В. Н. Яровенко, “Прогресс в химии азот-, кислород- и серасодержащих гетероциклических систем”, Усп. хим., 89:1 (2020), 55–124; N. N. Makhova, L. I. Belen'kii, G. A. Gazieva, I. L. Dalinger, L. S. Konstantinova, V. V. Kuznetsov, A. N. Kravchenko, M. M. Krayushkin, O. A. Rakitin, A. M. Starosotnikov, L. L. Fershtat, S. A. Shevelev, V. Z. Shirinian, V. N. Yarovenko, “Progress in the chemistry of nitrogen-, oxygen- and sulfur-containing heterocyclic systems”, Russian Chem. Reviews, 89:1 (2020), 55–124
Mohamed Ali Tabarki, Rafâa Besbes, “Selective synthesis of imidazolidine-2-thiones via ring expansion of aziridine-2-carboxylates with isothiocyanates”, Tetrahedron Letters, 57:34 (2016), 3832
Vivek Gupta, Vedhagiri Karthik, Ganapathi Anantharaman, “Labile dioxy-functionalised zwitterionic imidazolinium salt: access to zwitterionic and neutral imidazolidin-2-ylidene derivatives and π-acceptor properties of imidazolidine-2-selones”, RSC Adv., 5:107 (2015), 87888
V. V. Baranov, A. N. Kravchenko, Yu. V. Nelyubina, “Synthesis of new ring-fused thiocarbamates by condensation of 2-thioxo-and 2-oxo-1,3-dialkyl-4,5-dihydroxy-4,5-diphenylimidazolidines with KSCN”, Mendeleev Commun., 24:2 (2014), 105–107
A. N. Kravchenko, V. V. Baranov, Yu. V. Nelyubina, G. A. Gazieva, I. V. Svitan'ko, “Diastereoselective synthesis of 4,5-dihydroxyimidazolidin-2-ones (-thiones) and their structure”, Russ Chem Bull, 61:1 (2012), 64
G. A. Gazieva, V. V. Baranov, A. N. Kravchenko, N. N. Makhova, “α-Thioureidoalkylation of functionally substituted ureas: II. Synthesis of thio analogs of N-hydroxyalkyl-1,5-diphenylglycolurils”, Russ J Org Chem, 47:10 (2011), 1572
V. V. Baranov, G. A. Gazieva, Yu. V. Nelyubina, A. N. Kravchenko, N. N. Makhova, “α-Thioureidoalkylation of functionally substituted ureas: I. Tandem cyclization and esterification in reactions of N-(carboxyalkyl)ureas with 1,3-dialkyl-4,5-dihydroxy-4,5-diphenylimidazolidine-2-thiones in alcohols”, Russ J Org Chem, 47:10 (2011), 1564
Обратная связь: