Asymmetric 1,3-dipolar cycloaddition reaction of azomethine imines to allyl alcohol

Chemistry Letters

Volumn 37, Issue 3, 2008, Pages 342-343

  Kato, Tomomitsu ^a   Fujinami, Shuhei ^a   Ukaji, Yutaka ^a   Inomata, Katsuhiko ^a  

^a KANAZAWA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 42049087072     PISSN: 03667022     EISSN: None     Source Type: Journal    
DOI: 10.1246/cl.2008.342     Document Type: Article

References (30)

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27. 2Cl/80 °C/2 d/57%/90% ee.
28. 2 was added in the reaction in Table 2, Entry 1, 4a was obtained in 78% yield with 84% ee.
29. Although the 1,3-dipolar cycloaddition of 2a to (E)-2-buten-1-ol was carried out under similar conditions in Table 3, Entry 1 for 7d, the corresponding cycloadduct was not obtained.
30. w = 0.105) for 4539 reflections with I > 3.00σ(I) and 265 variable parameters. Supporting Information is available electronically on the CSJ-Journal Web site, http://www.csj.jp/journals/chem-lett.