Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Matt Rambla"'
Publikováno v:
European Journal of Organic Chemistry. 2014:7716-7720
The synthesis of chiral spiroimines, one of the pharmacophores of the marine neurotoxin gymnodimine A is described. The approach relies on a three-step sequence that includes a palladium-catalyzed asymmetric decarboxylative alkylation, an isomerizati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2819bd53338014cd09a89bd52bc66509
https://doi.org/10.1002/ejoc.201403161
https://doi.org/10.1002/ejoc.201403161
Publikováno v:
ChemInform. 46
The synthesis of optically active spiroimines, one of the pharmacophores of the marine neurotoxin gymnodimine A, is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03e7c2b011f0d02b535fdb9ac1809fc0
https://doi.org/10.1002/chin.201518110
https://doi.org/10.1002/chin.201518110
Publikováno v:
ChemInform. 45
The described method, giving a new stable class of 1,2-dispirodienone lactams, can be applied to a broad range of substrates with good yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b5463a7468bad7d3ddf93278e5aa1f2
https://doi.org/10.1002/chin.201416066
https://doi.org/10.1002/chin.201416066
Publikováno v:
Chemical Communications
Chemical Communications, Royal Society of Chemistry, 2013, 49 (98), pp.11542-11544. ⟨10.1039/c3cc47171c⟩
Chemical Communications, Royal Society of Chemistry, 2013, 49 (98), pp.11542-11544. ⟨10.1039/c3cc47171c⟩
1,2-Dispirodienones were synthesized by hypervalent iodine-mediated phenolic oxidation of p-hydroxy acetanilides. The reaction is compatible with several substituted anilides and affords a new class of 1,2-dispirodienones that are remarkably stable u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5785f1420e1b0a4ab1fb433cbc30234e
https://doi.org/10.1039/c3cc47171c
https://doi.org/10.1039/c3cc47171c