cheminform abstract: enantioselective bromoaminocyclization using amino—thiocarbamate catalysts

ChemInform 2011, 42, issue 46 © 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Pyrrole derivatives R 0120 DOI: 10.1002/chin.201146106 Enantioselective Bromoaminocyclization Using Amino—Thiocarbamate Cata- lysts. — The title process proceeds with synthetically useful yields and enantioselec- tivities. The method opens the route to the bicyclic aziridine (III) or the isoindolinone (X). — (ZHOU, L.; CHEN, J.; TAN, C. K.; YEUNG*, Y.-Y.; J. Am. Chem. Soc. 133 (2011) 24, 9164-9167, http://dx.doi.org/10.1021/ja201627h ; Dep. Chem., Natl. Univ. Singapore, Singapore 117543, Singapore; Eng.) — Kieslich 46- 106

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Page 1: ChemInform Abstract: Enantioselective Bromoaminocyclization Using Amino—Thiocarbamate Catalysts

Pyrrole derivativesR 0120 DOI: 10.1002/chin.201146106

Enantioselective Bromoaminocyclization Using Amino—Thiocarbamate Cata-lysts. — The title process proceeds with synthetically useful yields and enantioselec-tivities. The method opens the route to the bicyclic aziridine (III) or the isoindolinone (X). — (ZHOU, L.; CHEN, J.; TAN, C. K.; YEUNG*, Y.-Y.; J. Am. Chem. Soc. 133 (2011) 24, 9164-9167, http://dx.doi.org/10.1021/ja201627h ; Dep. Chem., Natl. Univ. Singapore, Singapore 117543, Singapore; Eng.) — Kieslich

46- 106

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