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Interrupted Baeyer–Villiger Rearrangement: Building A Stereoelectronic Trap for the Criegee Intermediate Научная публикация

Журнал Angewandte Chemie International Edition
ISSN: 1433-7851 , E-ISSN: 1521-3773
Вых. Данные Год: 2018, Том: 57, Номер: 13, Страницы: 3372-3376 Страниц : 5 DOI: 10.1002/anie.201712651
Авторы Vil Vera A. 1,3,4 , Gomes Gabriel dos Passos 2 , Bityukov Oleg V. 1,4 , Lyssenko Konstantin A. 5 , Nikishin Gennady I. 1 , Alabugin Igor V. 2 , Terent'ev Alexander O. 1,3,4
Организации
1 N. D. Zelinsky Institute of Organic Chemistry Russian Academy of Sciences 47 Leninsky prosp. 119991 Moscow Russian Federation
2 Department of Chemistry and Biochemistry Florida State University Tallahassee FL USA
3 D. I. Mendeleev University of Chemical Technology of Russia Moscow Russian Federation
4 All-Russian Research Institute for Phytopathology Moscow Region Russian Federation
5 A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 119991, Moscow, Russian Federation.

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
Идентификаторы БД:
≡ Web of science: WOS:000427235600014
≡ Scopus: 2-s2.0-85042383204
≡ OpenAlex: W2794244561
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