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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 |
Appears in Collections: | Staff Publications |
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