cheminform abstract: an exo- and enantioselective 1,3-dipolar cycloaddition of azomethine ylides...

ChemInform 2011, 42, issue 37 © 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Pyrrole derivatives R 0120 DOI: 10.1002/chin.201137105 An exo- and Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Ylides with Alkylidene Malonates Catalyzed by a N,O-Ligand/Cu(OAc)2-Derived Chiral Complex. — (WANG, M.; WANG, Z.; SHI, Y.-H.; SHI, X.-X.; FOSSEY, J. S.; DENG*, W.-P.; Angew. Chem., Int. Ed. 50 (2011) 21, 4897-4900, http://dx.doi.org/10.1002/anie.201007960 ; Sch. Pharm., East China Univ. Sci. Technol., Shanghai 200237, Peop. Rep. China; Eng.) — Bartels 37- 105

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Page 1: ChemInform Abstract: An exo- and Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Ylides with Alkylidene Malonates Catalyzed by a N,O-Ligand/Cu(OAc)2-Derived Chiral Complex

Pyrrole derivativesR 0120 DOI: 10.1002/chin.201137105

An exo- and Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Ylides with Alkylidene Malonates Catalyzed by a N,O-Ligand/Cu(OAc)2-Derived Chiral Complex. — (WANG, M.; WANG, Z.; SHI, Y.-H.; SHI, X.-X.; FOSSEY, J. S.; DENG*, W.-P.; Angew. Chem., Int. Ed. 50 (2011) 21, 4897-4900, http://dx.doi.org/10.1002/anie.201007960 ; Sch. Pharm., East China Univ. Sci. Technol., Shanghai 200237, Peop. Rep. China; Eng.) — Bartels

37- 105

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