Interrupted Baeyer–Villiger Rearrangement: Building A Stereoelectronic Trap for the Criegee Intermediate Научная публикация
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Angewandte Chemie International Edition
ISSN: 1433-7851 , E-ISSN: 1521-3773 |
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| Вых. Данные | Год: 2018, Том: 57, Номер: 13, Страницы: 3372-3376 Страниц : 5 DOI: 10.1002/anie.201712651 | ||||||||||
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Реферат:
The instability of hydroxy peroxyesters, the elusive Criegee intermediates of the Baeyer–Villiger rearrangement, can be alleviated by selective deactivation of the stereoelectronic effects that promote the 1,2-alkyl shift. Stable cyclic Criegee intermediates constrained within a five-membered ring can be prepared by mild reduction of the respective hydroperoxy peroxyesters (β-hydroperoxy-β-peroxylactones) which were formed in high yields in reaction of β-ketoesters with BF3⋅Et2O/H2O2.
Библиографическая ссылка:
Vil V.A.
, Gomes G.d.P.
, Bityukov O.V.
, Lyssenko K.A.
, Nikishin G.I.
, Alabugin I.V.
, Terent'ev A.O.
Interrupted Baeyer–Villiger Rearrangement: Building A Stereoelectronic Trap for the Criegee Intermediate
Angewandte Chemie International Edition. 2018. V.57. N13. P.3372-3376. DOI: 10.1002/anie.201712651 WOS Scopus OpenAlex
Interrupted Baeyer–Villiger Rearrangement: Building A Stereoelectronic Trap for the Criegee Intermediate
Angewandte Chemie International Edition. 2018. V.57. N13. P.3372-3376. DOI: 10.1002/anie.201712651 WOS Scopus OpenAlex
Идентификаторы БД:
| ≡ Web of science: | WOS:000427235600014 |
| ≡ Scopus: | 2-s2.0-85042383204 |
| ≡ OpenAlex: | W2794244561 |