Selective Syntheses of Bis[1,2]dithiolo[1,4]thiazines and Bis[1,2]dithiolopyrroles from Hünig's Base Научная публикация
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Journal of Organic Chemistry
ISSN: 1520-6904 , E-ISSN: 0022-3263 |
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| Вых. Данные | Год: 1998, Том: 63, Номер: 7, Страницы: 2189-2196 Страниц : 8 DOI: 10.1021/jo971864e | ||||||
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Реферат:
The reaction of N,N-diisopropylethylamine (Hünig's base) and disulfur dichloride in 1,2-dichloroethane, in the presence of DABCO, gives 4-ethylbis[1,2]dithiolo[5,4-b][4‘,5‘-e][1,4]thiazine-3,5-dithione (1), or, by addition of oxygen donors, the 3-oxo-5-thione 2 or 3,5-dione 3 derivatives are selectively obtained. When the first reaction is performed in boiling chlorobenzene, 4-ethylbis[1,2]dithiolo[4,5-b][5‘,4‘-d]pyrrole-3,5-dithione (4) is obtained by sulfur extrusion from 1, and in the presence of oxygen donors, the 3-oxo-5-thione 5 or 3,5-dione 6 derivatives are selectively obtained. Some interconversions of compounds 1−6 are described, and a coherent set of reaction pathways for the formation of all six products is proposed. X-ray diffraction shows that the new bis-dithiolothiazine ring system of 1−3 is folded out of planarity about the thiazine N−S vector, with the N-ethyl group folded back over the thiazine ring in a scorpion-like conformation. The new bis-dithiolopyrrole ring system of 4−6 is planar and extensively delocalized.
Библиографическая ссылка:
Rees C.W.
, White A.J.P.
, Williams D.J.
, Rakitin O.A.
, Marcos C.F.
, Polo C.
, Torroba T.
Selective Syntheses of Bis[1,2]dithiolo[1,4]thiazines and Bis[1,2]dithiolopyrroles from Hünig's Base
Journal of Organic Chemistry. 1998. V.63. N7. P.2189-2196. DOI: 10.1021/jo971864e WOS Scopus OpenAlex
Selective Syntheses of Bis[1,2]dithiolo[1,4]thiazines and Bis[1,2]dithiolopyrroles from Hünig's Base
Journal of Organic Chemistry. 1998. V.63. N7. P.2189-2196. DOI: 10.1021/jo971864e WOS Scopus OpenAlex
Идентификаторы БД:
| Web of science: | WOS:000073136500027 |
| Scopus: | 2-s2.0-0001441401 |
| OpenAlex: | W2950979634 |