cheminform abstract: the catalytic asymmetric 1,3-dipolar cycloaddition of ynones with azomethine...

ChemInform 2012, 43, issue 01 © 2012 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Pyrrole derivatives R 0120 DOI: 10.1002/chin.201201088 The Catalytic Asymmetric 1,3-Dipolar Cycloaddition of Ynones with Azomethine Ylides. — Aminomalonate (III) and α-aryl amino ester (VI) afford both a high enan- tioselectivity. Some selected dihydropyrrole products exhibit cytotoxicity towards car- cinoma cell lines. — (SHI, F.; LUO, S.-W.; TAO, Z.-L.; HE, L.; YU, J.; TU, S.-J.; GONG*, L.-Z.; Org. Lett. 13 (2011) 17, 4680-4683, http://dx.doi.org/10.1021/ol201898x ; Sch. Chem. Chem. Eng., Xuzhou Norm. Univ., Jiangsu, Xuzhou 221116, Peop. Rep. China; Eng.) — H. Simon 01- 088

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Page 1: ChemInform Abstract: The Catalytic Asymmetric 1,3-Dipolar Cycloaddition of Ynones with Azomethine Ylides

Pyrrole derivativesR 0120 DOI: 10.1002/chin.201201088

The Catalytic Asymmetric 1,3-Dipolar Cycloaddition of Ynones with Azomethine Ylides. — Aminomalonate (III) and α-aryl amino ester (VI) afford both a high enan-tioselectivity. Some selected dihydropyrrole products exhibit cytotoxicity towards car-cinoma cell lines. — (SHI, F.; LUO, S.-W.; TAO, Z.-L.; HE, L.; YU, J.; TU, S.-J.; GONG*, L.-Z.; Org. Lett. 13 (2011) 17, 4680-4683, http://dx.doi.org/10.1021/ol201898x ; Sch. Chem. Chem. Eng., Xuzhou Norm. Univ., Jiangsu, Xuzhou 221116, Peop. Rep. China; Eng.) — H. Simon

01- 088

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