Synthesis of 5,5-diallyl-substituted oxazolidin-2-one derivatives, based on reductive diallylation of amino acids Научная публикация
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Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285 |
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| Вых. Данные | Год: 2022, Том: 71, Номер: 3, Страницы: 580-583 Страниц : 4 DOI: 10.1007/s11172-022-3452-z | ||
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Реферат:
An efficient synthesis of 5,5-diallyl-substituted oxazolidinone derivatives, based on reductive diallylation of available α-amino acids, was developed. It was demonstrated that the obtained oxazolidinones can be readily converted into the corresponding derivatives of 3-azaspiro[4,4]-non-7-en-2-one via the metathesis reaction in the presence of the 1st generation Grubbs catalyst.
Библиографическая ссылка:
Klimenko R.V.
, Starykh S.A.
, Baranin S.V.
, Bubnov Y.N.
Synthesis of 5,5-diallyl-substituted oxazolidin-2-one derivatives, based on reductive diallylation of amino acids
Russian Chemical Bulletin. 2022. V.71. N3. P.580-583. DOI: 10.1007/s11172-022-3452-z WOS Scopus OpenAlex
Synthesis of 5,5-diallyl-substituted oxazolidin-2-one derivatives, based on reductive diallylation of amino acids
Russian Chemical Bulletin. 2022. V.71. N3. P.580-583. DOI: 10.1007/s11172-022-3452-z WOS Scopus OpenAlex
Идентификаторы БД:
| ≡ Web of science: | WOS:000787316800024 |
| ≡ Scopus: | 2-s2.0-85128822070 |
| ≡ OpenAlex: | W4224441403 |