| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1255525 | Chinese Chemical Letters | 2009 | 4 Pages |
Abstract
Highly efficient Michael addition reactions of malonates to nitroalkenes catalyzed by novel chiral thioureas derived from optically pure BINOL and amino acids are reported. Various trans-nitroalkenes reacted with malonates affording the desired products in up to 95% yield with excellent enantioselectivities (up to 97% ee).
Related Topics
Physical Sciences and Engineering
Chemistry
Chemistry (General)
Authors
Li Jun Yan, Quan Zhong Liu, Xue Lian Wang,