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<subfield code="a">Rodríguez Ferrer, Patricia</subfield>
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<subfield code="a">Sanz Novo, Miguel</subfield>
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<subfield code="a">Maestro Fernández, Alicia</subfield>
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<subfield code="a">Andrés García, José María</subfield>
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<subfield code="a">Pedrosa Sáez, Rafael</subfield>
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<subfield code="a">Enantioenriched 3‐amino‐3‐substituted oxindoles have been obtained by addition of different nucleophiles to N‐Boc ketimines derived from isatin catalyzed by chiral bifunctional supported thioureas. The Mannich reaction occurs with excellent enantioselection, but poor diastereoselection when prochiral nucleophiles were used. The supported catalyst were recovered and reused for five times without loss of activity. The mixture of diastereoisomers formed when a prochiral structure was used as nucleophile was converted into a single enantioenriched pyrazolyl derivative.</subfield>
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<subfield code="a">Advanced Synthesis and Catalysis, 2019, vol. 361, n. 15. p. 3645-3655</subfield>
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<subfield code="a">1615-4169</subfield>
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<subfield code="a">http://uvadoc.uva.es/handle/10324/37719</subfield>
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<subfield code="a">10.1002/adsc.201900414</subfield>
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<subfield code="a">Synthesis of Enantioenriched 3-Amino-3-Substituted Oxindoles by Stereoselective Mannich Reaction Catalyzed by Supported Bifunctional Thioureas</subfield>
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