Please use this identifier to cite or link to this item:
|Title:||Bicyclic guanidine-catalyzed direct asymmetric allylic addition of N-aryl alkylidene-succinimides|
|Citation:||Wang, J., Liu, H., Fan, Y., Yang, Y., Jiang, Z., Tan, C.-H. (2010-11-08). Bicyclic guanidine-catalyzed direct asymmetric allylic addition of N-aryl alkylidene-succinimides. Chemistry - A European Journal 16 (42) : 12534-12537. ScholarBank@NUS Repository. https://doi.org/10.1002/chem.201002183|
|Abstract:||Enantio-enriched maleimides and succinimides that can be used to prepare aza-heterocycles with multiple chiral centers are obtained from the bicyclic guanidine-catalyzed direct asymmetric allylic addition of N-aryl alkylidene-succinimides to imines. NMR studies and deuterium-exchange experiments were used to study the intermediates in the reaction. © 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.|
|Source Title:||Chemistry - A European Journal|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
checked on Dec 6, 2018
WEB OF SCIENCETM
checked on Nov 21, 2018
checked on Dec 8, 2018
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.