Please use this identifier to cite or link to this item:
|Title:||β-amino acid catalyzed asymmetric michael additions: Design of organocatalysts with catalytic acid/base dyad inspired by serine proteases|
|Authors:||Yang, H. |
|Citation:||Yang, H., Wong, M.W. (2011-09-16). β-amino acid catalyzed asymmetric michael additions: Design of organocatalysts with catalytic acid/base dyad inspired by serine proteases. Journal of Organic Chemistry 76 (18) : 7399-7405. ScholarBank@NUS Repository. https://doi.org/10.1021/jo2011413|
|Abstract:||A new type of chiral β-amino acid catalyst has been computationally designed, mimicking the enzyme catalysis of serine proteases. Our catalyst approach is based on the bioinspired catalytic acid/base dyad, namely, a carboxyl and imidazole pair. DFT calculations predict that this designed organocatalyst catalyzes Michael additions of aldehydes to nitroalkenes with excellent enantioselectivities and remarkably high anti diastereoselectivities. The unusual stacked geometry of the enamine intermediate, hydrogen bonding network, and the adoption of an exo transition state are the keys to understand the stereoselectivity. © 2011 American Chemical Society.|
|Source Title:||Journal of Organic Chemistry|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
checked on Jul 14, 2018
WEB OF SCIENCETM
checked on Jul 4, 2018
checked on Jun 29, 2018
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.