Please use this identifier to cite or link to this item:
https://scholarbank.nus.edu.sg/handle/10635/93145
| Title: | Asymmetric organocatalytic cascade Michael/hemiketalization/retro-Henry reaction of β,γ-unsaturated ketoesters with α-nitroketones | Authors: | Gao, Y. Ren, Q. Siau, W.-Y. Wang, J. |
Issue Date: | 28-May-2011 | Citation: | Gao, Y., Ren, Q., Siau, W.-Y., Wang, J. (2011-05-28). Asymmetric organocatalytic cascade Michael/hemiketalization/retro-Henry reaction of β,γ-unsaturated ketoesters with α-nitroketones. Chemical Communications 47 (20) : 5819-5821. ScholarBank@NUS Repository. | Abstract: | An unprecedented enantioselective organocatalytic Michael/hemiketalization/ retro-Henry cascade sequence is described, which catalyzed by a simple bifunctional indane amine-thiourea catalyst. This process provides a new route to the enantioselective synthesis of 5-nitro-pent-2-enoates, a precursor to α-ketolactam. © 2011 The Royal Society of Chemistry. | Source Title: | Chemical Communications | URI: | http://scholarbank.nus.edu.sg/handle/10635/93145 | ISSN: | 13597345 |
| Appears in Collections: | Staff Publications |
Show full item record
Files in This Item:
There are no files associated with this item.
Google ScholarTM
Check
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.