Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Dimitrios Zonidis"'
Publikováno v:
Organicbiomolecular chemistry. 19(29)
A series of 6-styryl-1,2-oxathiine 2,2-dioxides have been efficiently obtained by a two-step protocol from readily available (1E,4E)-1-(dimethylamino)-5-arylpenta-1,4-dien-3-ones involving a regioselective sulfene addition and subsequent Cope elimina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ebcbe83e5bf57686e2a5c600245d39a
https://pubmed.ncbi.nlm.nih.gov/34231619
https://pubmed.ncbi.nlm.nih.gov/34231619
Autor:
Mike W. J. Urquhart, Abby J. Mills, B. Mark Heron, Stuart Aiken, Ross J.L. Edgar, Lewis Cowen, Orlando D. C. C. de Azevedo, Craig R. Rice, Kelechi Anozie, Philippa A. Lawrence, Christopher D. Gabbutt, Dimitrios Zonidis
Publikováno v:
Organic & Biomolecular Chemistry. 17:9585-9604
Diversely substituted 1,2-oxathiine 2,2-dioxides, including 3,5,6-triaryl-, 3,6-diaryl-, 3,5-diaryl-, 5,6-diaryl- and selected fused heterocyclic analogues, have been efficiently obtained by the application of a mild Cope elimination of a 4-amino moi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2c27639f0b9031c0ab9898cc1bf566e
https://doi.org/10.1039/c9ob01657k
https://doi.org/10.1039/c9ob01657k
Publikováno v:
Organicbiomolecular chemistry. 17(44)
1,2-Oxathiine 2,2-dioxides have been obtained from their respective 3,4-dihydro-4-dimethylamino precursors, for the first time, by a mild Cope elimination of the 4-dimethylamino function. The application of the 1,2-oxathiine 2,2-dioxide scaffold in m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ad3a765ef0f02dc02a922e60864ae10
https://pubmed.ncbi.nlm.nih.gov/31681929
https://pubmed.ncbi.nlm.nih.gov/31681929