Highly Enantioselective Michael Addition of 3-Aryloxindoles to Phenyl Vinyl Sulfone Catalyzed by Cinchona Alkaloid-Derived Bifunctional Amine-Thiourea Catalysts Bearing Sulfonamide as Multiple Hydrogen-Bonding Donors
Zhao, Mei-Xin, Tang, Wen-Hao, Chen, Ming-Xiao, Wei, Deng-Ke, Dai, Tong-Lei, Shi, Min
Published in European Journal of Organic Chemistry (01.10.2011)
Published in European Journal of Organic Chemistry (01.10.2011)
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Published in European journal of organic chemistry (01.07.2012)
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Enantioselective Michael addition of 3-aryloxindoles to a vinyl bisphosphonate ester catalyzed by a cinchona alkaloid derived thiourea catalyst
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ChemInform Abstract: Enantioselective Michael Addition of 3-Aryloxindoles to a Vinyl Bisphosphonate Ester Catalyzed by a Cinchona Alkaloid Derived Thiourea Catalyst
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Published in ChemInform (05.03.2013)
Published in ChemInform (05.03.2013)
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ChemInform Abstract: Highly Enantioselective Michael Addition of 3-Aryloxindoles to Phenyl Vinyl Sulfone Catalyzed by Cinchona Alkaloid-Derived Bifunctional Amine-Thiourea Catalysts Bearing Sulfonamide as Multiple Hydrogen-Bonding Donors
Zhao, Mei-Xin, Tang, Wen-Hao, Chen, Ming-Xiao, Wei, Deng-Ke, Dai, Tong-Lei, Shi, Min
Published in ChemInform (20.03.2012)
Published in ChemInform (20.03.2012)
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Enantioselective Michael addition of 3-aryloxindoles to a vinyl bisphosphonate ester catalyzed by a cinchona alkaloid derived thiourea catalystElectronic supplementary information (ESI) available: NMR spectra of new compounds, HPLC traces for the determination of the enantiomeric excess for compounds 3, 5, 6, 8 and X-ray crystal data of product 3u. CCDC 867514. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c2ob25966d
Zhao, Mei-Xin, Dai, Tong-Lei, Liu, Ran, Wei, Deng-Ke, Zhou, Hao, Ji, Fei-Hu, Shi, Min
Year of Publication 20.09.2012
Year of Publication 20.09.2012
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