Please use this identifier to cite or link to this item:
|Title:||Amino-lndanol catalyzed enantioselective reactions of 3-hydroxy-2-pyridones|
|Source:||Julian, Y.-T.S., Tan, C.-H. (2009-05-27). Amino-lndanol catalyzed enantioselective reactions of 3-hydroxy-2-pyridones. Journal of the American Chemical Society 131 (20) : 6904-6905. ScholarBank@NUS Repository. https://doi.org/10.1021/ja900582a|
|Abstract:||A new bifunctional catalyst, chiral amino-indanol 1a, containing both Bronsted base and hydrogen bonding donor moieties, has been identified. It is easily prepared in a single step from commercially available amino-indanol. It was found to be an excellent catalyst for Diels-Alder reactions of both 3-hydroxy-2-pyridone and 3-hydroxy-2-pyrone. Various dienophiles including N-substituted maleimides were investigated. The Diels-Alder adducts were obtained in excellent yields and high enantioselectivities. Copyright © 2009 American Chemical Society.|
|Source Title:||Journal of the American Chemical Society|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
checked on Feb 13, 2018
WEB OF SCIENCETM
checked on Feb 19, 2018
checked on Feb 18, 2018
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.