Please use this identifier to cite or link to this item:
http://scholarbank.nus.edu.sg/handle/10635/75621
| 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 |
| Source: | 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/10635/75621 |
| ISSN: | 13597345 |
| Appears in Collections: | Staff Publications |
Show full item record
Files in This Item:
There are no files associated with this item.
SCOPUSTM
Citations
41
checked on Mar 8, 2018
WEB OF SCIENCETM
Citations
40
checked on Apr 18, 2018
Page view(s)
25
checked on Apr 20, 2018
Google ScholarTM
Check
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.