BF3 Mediated [1,5]‐Hydride Shift Triggered Cyclization: Thioethers Join the Game Научная публикация
| Журнал |
European Journal of Organic Chemistry
ISSN: 1434-193X , E-ISSN: 1099-0690 |
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| Вых. Данные | Год: 2022, Том: 2022, Номер: 25, Номер статьи : e202200547, Страниц : DOI: 10.1002/ejoc.202200547 | ||||||||
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Реферат:
2-(2-(Benzylthio)benzylidene)malonates can undergo the 1,5-hydride shift triggered cyclization resulting in thiachromanes in 45–84 % yield. Boron trifluoride as a reaction promotor is the key to success. DFT calculations revealed that the reaction proceeds via a chelate BF2 complex, which was confirmed by NMR-analysis. Experimental and theoretical comparison of nitrogen, sulfur and carbon analogues revealed that sulfur derivatives have the highest activation barrier for the hydride transfer due to the unfavorable transition state geometry, which explains the lack of previous reports on 1,5-hydride shifts in (alkylthio)styrenes.
Библиографическая ссылка:
Zaitseva E.R.
, Smirnov A.Y.
, Timashev V.I.
, Malyshev V.I.
, Zhigileva E.A.
, Mikhaylov A.A.
, Medvedev M.G.
, Baleeva N.S.
, Baranov M.S.
BF3 Mediated [1,5]‐Hydride Shift Triggered Cyclization: Thioethers Join the Game
European Journal of Organic Chemistry. 2022. V.2022. N25. e202200547 . DOI: 10.1002/ejoc.202200547 WOS Scopus OpenAlex
BF3 Mediated [1,5]‐Hydride Shift Triggered Cyclization: Thioethers Join the Game
European Journal of Organic Chemistry. 2022. V.2022. N25. e202200547 . DOI: 10.1002/ejoc.202200547 WOS Scopus OpenAlex
Идентификаторы БД:
| ≡ Web of science: | WOS:000819991400001 |
| ≡ Scopus: | 2-s2.0-85133586645 |
| ≡ OpenAlex: | W4280523808 |