Divergent Annulations of 5,6‐Dihydro‐4H‐1,2‐Oxazine N‐Oxides and Enol Diazoacetates for the Switchable Chemoselective Synthesis of Fused 1,2‐Oxazine Derivatives Научная публикация
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European Journal of Organic Chemistry
ISSN: 1434-193X , E-ISSN: 1099-0690 |
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| Вых. Данные | Год: 2024, Том: 27, Номер: 45, Номер статьи : e202400768, Страниц : DOI: 10.1002/ejoc.202400768 | ||||||
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Реферат:
Reactions of 5,6-dihydro-4H-1,2-oxazine N-oxides with enol diazoacetates were studied. A particular reaction path depends on the amount of catalyst and the order of the addition of the substrates. Use of Rh2(Oct)4 (2 mol.%) leads to chemoselective [3+3]-annulation producing 1,2-oxazine-fused 1,2-oxazine derivatives. With lower catalyst loadings (0.03 mol.%) enol diazoacetates are converted to cyclopropene derivatives, which in situ react with 1,2-oxazine N-oxides via tandem [3+2]-cycloaddition-rearrangement producing oxazine-fused aziridines. Both transformations showed a wide substrate scope and produced target products with good yields and diastereoselectivity, thus allowing selective preparation of these rare heterocyclic systems. A mechanistic rationale for observed chemo- and stereo- selectivities was proposed.
Библиографическая ссылка:
Ostarkov S.N.
, Lichtenstein Y.I.
, Antonova Y.A.
, Nelyubina Y.V.
, Lesnikov V.K.
, Tabolin A.A.
Divergent Annulations of 5,6‐Dihydro‐4H‐1,2‐Oxazine N‐Oxides and Enol Diazoacetates for the Switchable Chemoselective Synthesis of Fused 1,2‐Oxazine Derivatives
European Journal of Organic Chemistry. 2024. V.27. N45. e202400768 . DOI: 10.1002/ejoc.202400768 WOS Scopus OpenAlex
Divergent Annulations of 5,6‐Dihydro‐4H‐1,2‐Oxazine N‐Oxides and Enol Diazoacetates for the Switchable Chemoselective Synthesis of Fused 1,2‐Oxazine Derivatives
European Journal of Organic Chemistry. 2024. V.27. N45. e202400768 . DOI: 10.1002/ejoc.202400768 WOS Scopus OpenAlex
Идентификаторы БД:
| ≡ Web of science: | WOS:001357552000001 |
| ≡ Scopus: | 2-s2.0-85208502364 |
| ≡ OpenAlex: | W4403253617 |