Synthesis of functionalized organophosphorus analogs of β-phenylalanine Научная публикация
| Журнал |
Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285 |
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| Вых. Данные | Год: 2024, Том: 73, Номер: 5, Страницы: 1374-1385 Страниц : 12 DOI: 10.1007/s11172-024-4255-1 | ||||||
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Реферат:
A convenient synthesis of organophosphorus analogs of β-phenylalanine containing functionalized 2-phenylethylphosphonous and 2-phenylethylphosphinic acid moieties has been developed. The radical addition of bis(trimethylsiloxy)phosphine to styrene, trimethylsilyl cinnamate, or arylacetylenes proceeds regioselectively to give a variety of substituted 2-phenylethylphosphonites, and the subsequent functionalization affords various derivatives of the target acids. The resulting compounds are of interest as promising biologically active compounds and water-soluble ligands.
Библиографическая ссылка:
Bubnov Y.N.
, Prishchenko A.A.
, Livantsov M.V.
, Novikova O.P.
, Livantsova L.I.
, Baranin S.V.
Synthesis of functionalized organophosphorus analogs of β-phenylalanine
Russian Chemical Bulletin. 2024. V.73. N5. P.1374-1385. DOI: 10.1007/s11172-024-4255-1 WOS Scopus OpenAlex
Synthesis of functionalized organophosphorus analogs of β-phenylalanine
Russian Chemical Bulletin. 2024. V.73. N5. P.1374-1385. DOI: 10.1007/s11172-024-4255-1 WOS Scopus OpenAlex
Идентификаторы БД:
| ≡ Web of science: | WOS:001252371600019 |
| ≡ Scopus: | 2-s2.0-85196560917 |
| ≡ OpenAlex: | W4399897712 |