Please use this identifier to cite or link to this item: https://doi.org/10.1055/s-0033-1338434
Title: Highly enantioselective Michael addition of α-substituted nitrophosphonates to a vinyl sulfone
Authors: Chen, G.-Y.
Lu, Y. 
Keywords: cinchona alkaloid
Michael Addition
nitrophosphonate
thiourea
vinyl sulfone
Issue Date: 2013
Citation: Chen, G.-Y., Lu, Y. (2013). Highly enantioselective Michael addition of α-substituted nitrophosphonates to a vinyl sulfone. Synthesis (Germany) 45 (12) : 1654-1658. ScholarBank@NUS Repository. https://doi.org/10.1055/s-0033-1338434
Abstract: Organocatalytic asymmetric Michael reaction of α-substituted nitrophosphonates to phenyl vinyl sulfone catalyzed by cinchona alkaloid-derived tertiary amine-thioureas afforded α,α-disubstituted nitrophosphonates in very good yields and excellent enantiomeric excesses. © Georg Thieme Verlag Stuttgart, New York.
Source Title: Synthesis (Germany)
URI: http://scholarbank.nus.edu.sg/handle/10635/93944
ISSN: 00397881
DOI: 10.1055/s-0033-1338434
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