Please use this identifier to cite or link to this item:
|Title:||Bifunctional thiourea-promoted cascade aza-Michael-Henry-dehydration reactions: Asymmetric preparation of 3-nitro-1,2-dihydroquinolines|
|Citation:||Liu, X., Lu, Y. (2010-09-21). Bifunctional thiourea-promoted cascade aza-Michael-Henry-dehydration reactions: Asymmetric preparation of 3-nitro-1,2-dihydroquinolines. Organic and Biomolecular Chemistry 8 (18) : 4063-4065. ScholarBank@NUS Repository. https://doi.org/10.1039/c0ob00223b|
|Abstract:||A cascade aza-Michael-Henry-dehydration reaction catalyzed by quinidine-derived tertiary amine-thiourea catalyst was developed via installation of suitable electron withdrawing groups at the amino function of aniline. This strategy led to a one-step preparation of chiral 3-nitro-1,2-dihydroquinolines in high yields and with up to 90% enantiomeric excesses. © 2010 The Royal Society of Chemistry.|
|Source Title:||Organic and Biomolecular Chemistry|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
checked on Jan 22, 2019
WEB OF SCIENCETM
checked on Jan 2, 2019
checked on Jan 12, 2019
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.