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|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|
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