Synthesis of enantiopure substituted piperidines via an aziridinium ring expansion

Organic Letters

Volumn 13, Issue 15, 2011, Pages 3830-3833

  Jarvis, Scott B D ^a   Charette, Andre B ^a  

^a UNIVERSITÉ DE MONTRÉAL   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

AZIRIDINE; AZIRIDINE DERIVATIVE; PIPERIDINE DERIVATIVE;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; STEREOISOMERISM; SYNTHESIS;

AZIRIDINES; MOLECULAR STRUCTURE; PIPERIDINES; STEREOISOMERISM;

EID: 79961033802     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol201349k     Document Type: Article

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46. The products in entries 1 and 3 of Table 2 were determined to be >99% ee (SFC on chiral stationary phase). Entries 4 and 5 combined two enantiopure precursors to obtain the intermediate as a single diastereomer.