Stereoselective cross-coupling between allylic alcohols and aldimines

Organic Letters

Volumn 11, Issue 14, 2009, Pages 3132-3134

  Lysenko, Ivan L ^a   Lee, Hyung Goo ^a   Cha, Jin Kun ^a  

^a WAYNE STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 67650293065     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol901006c     Document Type: Article

References (34)

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31. (a) Amine 13 was independently prepared by the Claisen-Ireland rearrangement of the phenyl acetate of (S)-7, followed by the Curtius rearrangement, hydrolysis, and reductive amination with benzaldehyde.
32. (b) The relative stereochemistry was also established by measurement of the key vicinal coupling constant of a tetrahydropyridine derived from 5c via allylation and ring-closing metathesis.
33. (c) See Supporting Information for these stereochemical studies.
34. During the course of manuscript preparation, a related study was reported by Professor Micalizio: Takahashi, M.; McLaughlin, M.; Micalizio, G. C. Angew. Chem., Int. Ed 2009, 48, 3648.