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Volumn 50, Issue 26, 2009, Pages 3329-3332

Enantioselective aziridination reaction of α,β-unsaturated aldehydes using an organocatalyst and tert-butyl N-arenesulfonyloxycarbamates

Author keywords

[No Author keywords available]

Indexed keywords

ACETIC ACID; ALDEHYDE DERIVATIVE; AROMATIC CARBOXYLIC ACID; AZIRIDINE DERIVATIVE; CARBAMIC ACID DERIVATIVE; SODIUM CARBONATE; TERT BUTYL N ARENESULFONYLOXYCARBAMATE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 65549136308     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.02.095     Document Type: Article
Times cited : (73)

References (43)
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    • For a review of aziridines, see:
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    • Sweeney, J.B.1
  • 2
    • 17644415303 scopus 로고    scopus 로고
    • For reviews on the synthesis of aziridines, see:
    • For reviews on the synthesis of aziridines, see:. Halfen J.A. Curr. Org. Chem. 9 (2005) 657-669
    • (2005) Curr. Org. Chem. , vol.9 , pp. 657-669
    • Halfen, J.A.1
  • 5
    • 1542375289 scopus 로고    scopus 로고
    • For synthetic applications of aziridines, see:
    • For synthetic applications of aziridines, see:. Hu X.E. Tetrahedron 60 (2004) 2701-2743
    • (2004) Tetrahedron , vol.60 , pp. 2701-2743
    • Hu, X.E.1
  • 8
    • 34547843706 scopus 로고    scopus 로고
    • For recent examples of enantioselective aziridination, see:
    • For recent examples of enantioselective aziridination, see:. Yamawaki M., Tanaka M., Abe T., Anada M., and Hashimoto S. Heterocycles 72 (2007) 709-721
    • (2007) Heterocycles , vol.72 , pp. 709-721
    • Yamawaki, M.1    Tanaka, M.2    Abe, T.3    Anada, M.4    Hashimoto, S.5
  • 14
    • 33845500079 scopus 로고    scopus 로고
    • For recent examples of organocatalytic aziridinations, see:
    • For recent examples of organocatalytic aziridinations, see:. Shen Y.-M., Zhao M.-X., Xu J., and Shi Y. Angew. Chem., Int. Ed. 45 (2006) 8005-8008
    • (2006) Angew. Chem., Int. Ed. , vol.45 , pp. 8005-8008
    • Shen, Y.-M.1    Zhao, M.-X.2    Xu, J.3    Shi, Y.4
  • 18
    • 34547623607 scopus 로고    scopus 로고
    • For reviews on organocatalysts, see:
    • For reviews on organocatalysts, see:. Pellissier H. Tetrahedron 63 (2007) 9267-9331
    • (2007) Tetrahedron , vol.63 , pp. 9267-9331
    • Pellissier, H.1
  • 28
    • 0000603208 scopus 로고
    • For aziridinations using N-arenesulfonyloxycarbamates, see:
    • For aziridinations using N-arenesulfonyloxycarbamates, see:. Lwowski W., and Mairich T.J. J. Am. Chem. Soc. 87 (1965) 3630-3637
    • (1965) J. Am. Chem. Soc. , vol.87 , pp. 3630-3637
    • Lwowski, W.1    Mairich, T.J.2
  • 39
    • 65549150803 scopus 로고    scopus 로고
    • note
    • Although N-arenesulfonyloxycarbamates afforded aziridine aldehydes with a high diastereoselectivity, the origin of the high diastereoselectivity is unclear.
  • 43
    • 65549121129 scopus 로고    scopus 로고
    • note
    • R = 10.7 min (minor) and 13.6 min (major).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.