Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Michael S. Meyers"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 12, Iss 1, Pp 2032-2037 (2016)
Efficient one-pot Ugi–Smiles couplings are reported for the use of furyl-substituted aldehyde components. In the presence of these heterocyclic aldehydes, reactions tolerated variations in amine components and led to either isolated N-arylamide Ugi
Externí odkaz:
https://doaj.org/article/324d45fe58b241d39eb2605b50424545
Publikováno v:
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 12, Iss 1, Pp 2032-2037 (2016)
Beilstein Journal of Organic Chemistry, Vol 12, Iss 1, Pp 2032-2037 (2016)
Efficient one-pot Ugi–Smiles couplings are reported for the use of furyl-substituted aldehyde components. In the presence of these heterocyclic aldehydes, reactions tolerated variations in amine components and led to either isolated N-arylamide Ugi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e66e085498c44f8c5db419f3781902c
http://europepmc.org/articles/PMC5082724
http://europepmc.org/articles/PMC5082724
Publikováno v:
Tetrahedron Letters. 57:492-494
Use of allylamine and substituted 2-furaldehydes as components in Ugi–Smiles couplings of 2-nitrophenol provide ready access to N-aryl epoxyisoindolines. These adducts form via a dual event involving the Ugi–Smiles multicomponent reaction and an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3076b2159d99beaddc513f4401fad53d
https://doi.org/10.1016/j.tetlet.2015.12.068
https://doi.org/10.1016/j.tetlet.2015.12.068
Publikováno v:
ChemInform. 47
Efficient one-pot Ugi–Smiles couplings are reported for the use of furyl-substituted aldehyde components. In the presence of these heterocyclic aldehydes, reactions tolerated variations in amine components and led to either isolated N-arylamide Ugi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7fbb46505f1229e71f78cebf75c29aca
https://doi.org/10.1002/chin.201648058
https://doi.org/10.1002/chin.201648058
Publikováno v:
ChemInform. 47
Use of allylamine and substituted 2-furaldehydes as components in Ugi–Smiles couplings of 2-nitrophenol provide ready access to N-aryl epoxyisoindolines. These adducts form via a dual event involving the Ugi–Smiles multicomponent reaction and an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4e3bbb18bf9ea3b54114ccb58d8257f
https://doi.org/10.1002/chin.201620104
https://doi.org/10.1002/chin.201620104