Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Zainab Al-Jaroudi"'
Publikováno v:
Synthesis. 48:4477-4488
Further synthetic utility of 3-substituted N-arylisoindolinones obtained from N-aryl-3-hydroxyisoindolinones and alkyl aryl ketones under Lewis acid mediated anhydrous conditions is reported. Herein, substituted 6,6a-dihydroisoindolo[2,1-a]quinolin-1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::73a76fac10f2104cd53c3127b47229a4
https://doi.org/10.1055/s-0035-1562616
https://doi.org/10.1055/s-0035-1562616
Publikováno v:
Tetrahedron Letters. 57:772-777
The reactions of N-aryl-3-hydroxyisoindolinones and alkyl aryl ketones under Lewis acid-catalyzed anhydrous conditions afforded the corresponding substituted isoindolinones in good to excellent yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::339034820ff78646a5dcebabb4effe0d
https://doi.org/10.1016/j.tetlet.2016.01.021
https://doi.org/10.1016/j.tetlet.2016.01.021
Publikováno v:
ChemInform. 47
The reactions of N-aryl-3-hydroxyisoindolinones and alkyl aryl ketones under Lewis acid-catalyzed anhydrous conditions afforded the corresponding substituted isoindolinones in good to excellent yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6f33c61bf0393d11d6c7122103a4789
https://doi.org/10.1002/chin.201623129
https://doi.org/10.1002/chin.201623129
Publikováno v:
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 10, Iss 1, Pp 848-857 (2014)
Beilstein Journal of Organic Chemistry, Vol 10, Iss 1, Pp 848-857 (2014)
The synthesis of 5-substituted 6,6a-dihydroisoindolo[2,1-a]quinolin-11(5H)-ones via [4 + 2] imino-Diels–Alder cyclization from N-aryl-3-hydroxyisoindolinones and N-vinyl lactams under Lewis acid-catalysed anhydrous conditions is reported. Reactions
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6e4436b1b1aa13af43d7ed425cd5f40
https://pubmed.ncbi.nlm.nih.gov/24778740
https://pubmed.ncbi.nlm.nih.gov/24778740