Please use this identifier to cite or link to this item:
|Title:||Expeditious diastereoselective construction of a thiochroman skeleton via a cinchona alkaloid-derived catalyst|
|Citation:||Du, Z., Zhou, C., Gao, Y., Ren, Q., Zhang, K., Cheng, H., Wang, W., Wang, J. (2012-01-07). Expeditious diastereoselective construction of a thiochroman skeleton via a cinchona alkaloid-derived catalyst. Organic and Biomolecular Chemistry 10 (1) : 36-39. ScholarBank@NUS Repository. https://doi.org/10.1039/c1ob06497e|
|Abstract:||An example of diastereoselective and enantioselective synthesis of thiochroman derivatives through a sulfa-Michael-Michael cascade sequence is disclosed. This is a significant complement of the quinine-thiourea catalyzed sulfa-Michael-Michael cascade reaction. The densely functionalized target thiochromans were obtained in high diastereoselectivities, and with high to excellent enantioselectivities.|
|Source Title:||Organic and Biomolecular Chemistry|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
checked on Oct 16, 2018
WEB OF SCIENCETM
checked on Oct 8, 2018
checked on Oct 5, 2018
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.