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Issue 38, 2014
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Diastereoselective synthesis of functionalized pyrrolidines through N-bromosuccinimide-induced aziridine ring expansion cascade of cinnamylaziridine

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Abstract

An efficient aziridine ring expansion cascade of cinnamylaziridine has been developed. N-Bromosuccinimide was used as the promoter. The resulting functionalized pyrrolidines are the fundamental units of many useful molecules.

Graphical abstract: Diastereoselective synthesis of functionalized pyrrolidines through N-bromosuccinimide-induced aziridine ring expansion cascade of cinnamylaziridine

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Publication details

The article was received on 02 Jul 2014, accepted on 06 Aug 2014 and first published on 06 Aug 2014


Article type: Communication
DOI: 10.1039/C4OB01384K
Citation: Org. Biomol. Chem., 2014,12, 7482-7485
  • Open access: Creative Commons BY-NC license
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    Diastereoselective synthesis of functionalized pyrrolidines through N-bromosuccinimide-induced aziridine ring expansion cascade of cinnamylaziridine

    J. Zhou and Y. Yeung, Org. Biomol. Chem., 2014, 12, 7482
    DOI: 10.1039/C4OB01384K

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