Аннотация:
The Pummerer rearrangement of 4,4-dimethyl-1,4-thiasilinane 1-oxide affords 4,4-dimethyl-3,4-dihydro-2H-1,4-thiasiline, the first cyclic organosilicon vinyl sulfide.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
E. N. Suslova, B. A. Shainyan, “4,4-Dimethyl-3,4-dihydro-2H-1,4-thiasiline – the first cyclic organosilicon vinyl sulfide”, Mendeleev Commun., 23:5 (2013), 255–256
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc2680
https://www.mathnet.ru/rus/mendc/v23/i5/p255
Эта публикация цитируется в следующих 5 статьяx:
Bagrat A. Shainyan, “Silacyclohexanes, Sila(hetero)cyclohexanes and Related Compounds: Structure and Conformational Analysis”, Molecules, 25:7 (2020), 1624
E. N. Suslova, B. A. Shainyan, “S-functional derivatives of 3,4-dihydro-2H-1,4-thiasilines”, Russ J Gen Chem, 85:12 (2015), 2743
Elena N. Suslova, Bagrat A. Shainyan, “Synthesis of 4,4-diphenyl-3,4-dihydro-2H-1,4-thiasiline”, Journal of Sulfur Chemistry, 35:6 (2014), 641
Elena N. Suslova, Bagrat A. Shainyan, “ChemInform Abstract: 4,4‐Dimethyl‐3,4‐dihydro‐2H‐1,4‐thiasiline — The First Cyclic Organosilicon Vinyl Sulfide.”, ChemInform, 45:12 (2014)
B. A. Shainyan, E. Kleinpeter, “Conformational flexibility of 4,4-dimethyl-3,4-dihydro-2H-1,4-thiasiline and its monoheterocyclic analogs”, Russ J Gen Chem, 84:7 (2014), 1325
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