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Volumn 7, Issue 5, 2010, Pages 353-359

Synthesis of the azetidinyl-thiazoline fragment of vioprolides A and C

Author keywords

Antifungal metabolites; Azetidines; Natural products

Indexed keywords


EID: 77955970832     PISSN: 15701786     EISSN: None     Source Type: Journal    
DOI: 10.2174/157017810791514814     Document Type: Article
Times cited : (8)

References (10)
  • 2
    • 0346100660 scopus 로고    scopus 로고
    • Chemical basis for the biological activity of Imexon and related cyanoaziridines
    • For similar condensations, see a) Iyengar, B. S.; Dorr, R. T.; Remers, W.; A. Chemical basis for the biological activity of Imexon and related cyanoaziridines. J. Med. Chem. 2004, 47, 218.
    • (2004) J. Med. Chem. , vol.47 , pp. 218
    • Iyengar, B.S.1    Dorr, R.T.2    Remers, W.A.3
  • 4
    • 0037066118 scopus 로고    scopus 로고
    • A straightforward synthesis of enantiopure 2-cyano azetidines from β-amino alcohols
    • Agami, C.; Couty, F.; Evano, G. A straightforward synthesis of enantiopure 2-cyano azetidines from β-amino alcohols. Tetrahedron Asymmetry, 2002, 13, 297.
    • (2002) Tetrahedron Asymmetry , vol.13 , pp. 297
    • Agami, C.1    Couty, F.2    Evano, G.3
  • 5
    • 72049122384 scopus 로고    scopus 로고
    • Azetidines: New tools for the synthesis of nitrogen heterocycles
    • For a recent review on the chemistry of azetidines based on this methodology, see: Couty, F.; Evano, G. Azetidines: new tools for the synthesis of nitrogen heterocycles. Synlett, 2009, 19, 3053.
    • (2009) Synlett , vol.19 , pp. 3053
    • Couty, F.1    Evano, G.2
  • 6
    • 0003405157 scopus 로고
    • Georg Thieme Verlag Stuttgart: New York
    • Kociensky, P. J. Protecting Groups, Georg Thieme Verlag Stuttgart: New York, 1994.
    • (1994) Protecting Groups
    • Kociensky, P.J.1
  • 9
    • 58449107617 scopus 로고    scopus 로고
    • Highly enantioselective synthesis of β-amino alcohols
    • For a recent review on this topic, see: Metro, T. X.; Pardo, D. G.; Cossy, J. Highly enantioselective synthesis of β-amino alcohols. Chem. Eur. J. 2009, 15, 1064.
    • (2009) Chem. Eur. J. , vol.15 , pp. 1064
    • Metro, T.X.1    Pardo, D.G.2    Cossy, J.3
  • 10
    • 58149323439 scopus 로고
    • Chiral oxazolidinones from N-Boc derivatives of β-amino alcohols: Effect of a N-methyl substituent on reactivity and stereoselectivity
    • Agami, C.; Couty, F, Hamon, L., Venier, O. Chiral oxazolidinones from N-Boc derivatives of β-amino alcohols: effect of a N-methyl substituent on reactivity and stereoselectivity. Bull. Soc. Chem. Fr., 1995, 132, 808.
    • (1995) Bull. Soc. Chem. Fr. , vol.132 , pp. 808
    • Agami, C.1    Couty, F.2    Hamon, L.3    Venier, O.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.