Please use this identifier to cite or link to this item:
https://hdl.handle.net/10356/97284| Title: | Enantioselective activation of stable carboxylate esters as enolate equivalents via N-heterocyclic carbene catalysts | Authors: | Hao, Lin Du, Yu Lv, Hui Chen, Xingkuan Jiang, Huishen Shao, Yaling Chi, Robin Yonggui |
Issue Date: | 2012 | Source: | Hao, L., Du, Y., Lv, H., Chen, X., Jiang, H., Shao, Y., et al. (2012). Enantioselective Activation of Stable Carboxylate Esters as Enolate Equivalents via N-Heterocyclic Carbene Catalysts. Organic Letters, 14(8), 2154-2157. | Series/Report no.: | Organic letters | Abstract: | The first N-Heterocyclic Carbene (NHC) mediated activation of stable carboxylate esters to generate enolate intermediates is disclosed. The catalytically generated arylacetic ester enolates undergo enantioselective reactions with α,β-unsaturated imines. | URI: | https://hdl.handle.net/10356/97284 http://hdl.handle.net/10220/10637 |
ISSN: | 1523-7060 | DOI: | 10.1021/ol300676w | Schools: | School of Physical and Mathematical Sciences | Rights: | © 2012 American Chemical Society. | Fulltext Permission: | none | Fulltext Availability: | No Fulltext |
| Appears in Collections: | SPMS Journal Articles |
SCOPUSTM
Citations
5
181
Updated on Apr 20, 2025
Web of ScienceTM
Citations
5
169
Updated on Oct 30, 2023
Page view(s) 5
1,154
Updated on May 5, 2025
Google ScholarTM
Check
Altmetric
Items in DR-NTU are protected by copyright, with all rights reserved, unless otherwise indicated.