Please use this identifier to cite or link to this item: https://doi.org/10.1039/c1ob06497e
Title: Expeditious diastereoselective construction of a thiochroman skeleton via a cinchona alkaloid-derived catalyst
Authors: Du, Z.
Zhou, C.
Gao, Y.
Ren, Q.
Zhang, K.
Cheng, H.
Wang, W.
Wang, J. 
Issue Date: 7-Jan-2012
Source: 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
URI: http://scholarbank.nus.edu.sg/handle/10635/76154
ISSN: 14770520
DOI: 10.1039/c1ob06497e
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