cheminform abstract: organocatalytic asymmetric α-amination of unprotected 3-aryl and 3-aliphatic...

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ChemInform 2012, 43, issue 18 © 2012 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Indole derivatives R 0140 DOI: 10.1002/chin.201218124 Organocatalytic Asymmetric α-Amination of Unprotected 3-Aryl and 3-Aliphatic Substituted Oxindoles Using Di-tert-butyl Azodicarboxylate. — (ZHOU, F.; DING, M.; LIU, Y.-L.; WANG, C.-H.; JI, C.-B.; ZHANG, Y.-Y.; ZHOU*, J.; Adv. Synth. Catal. 353 (2011) 16, 2945-2952, http://dx.doi.org/10.1002/adsc.201100379 ; Shanghai Key Lab. Green Chem. Chem. Process, East China Norm. Univ., Shanghai 200062, Peop. Rep. China; Eng.) — Nuesgen 18- 124

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Page 1: ChemInform Abstract: Organocatalytic Asymmetric α-Amination of Unprotected 3-Aryl and 3-Aliphatic Substituted Oxindoles Using Di-tert-butyl Azodicarboxylate

Indole derivativesR 0140 DOI: 10.1002/chin.201218124

Organocatalytic Asymmetric α-Amination of Unprotected 3-Aryl and 3-Aliphatic Substituted Oxindoles Using Di-tert-butyl Azodicarboxylate. — (ZHOU, F.; DING, M.; LIU, Y.-L.; WANG, C.-H.; JI, C.-B.; ZHANG, Y.-Y.; ZHOU*, J.; Adv. Synth. Catal. 353 (2011) 16, 2945-2952, http://dx.doi.org/10.1002/adsc.201100379 ; Shanghai Key Lab. Green Chem. Chem. Process, East China Norm. Univ., Shanghai 200062, Peop. Rep. China; Eng.) — Nuesgen

18- 124

ChemInform 2012, 43, issue 18 © 2012 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim

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