کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1314079 | 1499331 | 2015 | 6 صفحه PDF | دانلود رایگان |
• The fluorous bis(oxazolines) was found to be a general, highly enantioselective ligand for the intramolecular amidation of imines.
• A series of chiral dihydroquinazolinones were obtained in 76–94% yields with enantioselectivities up to 98%.
• The fluorous ligand can be easily recovered and reused at least three times without significant loss of enantioselectivity.
A Sc(OTf)3-catalyzed intramolecular amidation of imines with a novel fluorous bis(oxazolines) as ligand is presented. The corresponding chiral dihydroquinazolinones were obtained in 76–94% yield with enantioselectivities up to 98%. The fluorous ligand can be easily recovered and reused at least three times without significant loss of enantioselectivity.
A Sc(OTf)3-catalyzed intramolecular amidation of imines with a novel fluorous bis(oxazolines) as ligand is presented. The corresponding chiral dihydroquinazolinones were obtained in 76–94% yield with enantioselectivities up to 98%. The fluorous ligand can be easily recovered and reused at least 3 times without significant loss of enantioselectivity.Figure optionsDownload as PowerPoint slide
Journal: Journal of Fluorine Chemistry - Volume 169, January 2015, Pages 72–77