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Volumn 25, Issue 1, 2006, Pages 31-38

Chemoenzymatic enantioselective formal synthesis of (-)-gephyrotoxin-223

Author keywords

Alkaloids; Candida Antartica Lipse; Chemoenzymatic; Desymmetrization; Gephyrotoxin; Indolizidine

Indexed keywords


EID: 33745456709     PISSN: 10219986     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (9)

References (8)
  • 1
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    • Thirty years of discovering arthropod alkaloids in amphibian skin
    • Daly, J. W., Thirty years of discovering arthropod alkaloids in amphibian skin, J. Nat. Prod., 61, p.162 (1998).
    • (1998) J. Nat. Prod. , vol.61 , pp. 162
    • Daly, J.W.1
  • 2
    • 77956653175 scopus 로고    scopus 로고
    • Edited by Cordell, G. A., Academic Press
    • Daly, J. W., "The Alkaloids", Edited by Cordell, G. A., Academic Press, 50, pp. 141-169 (1998).
    • (1998) The Alkaloids , vol.50 , pp. 141-169
    • Daly, J.W.1
  • 3
    • 0038729025 scopus 로고    scopus 로고
    • Chemoenzymatic enantioselective synthesis of (-)-indolizidine 167 B
    • Chênevert, R., Mohammadi Ziarani, G., Dasser, M., Chemoenzymatic Enantioselective Synthesis of (-)-Indolizidine 167 B, Heterocycles, 50, p. 593 (1999).
    • (1999) Heterocycles , vol.50 , pp. 593
    • Chênevert, R.1    Mohammadi Ziarani, G.2    Dasser, M.3
  • 4
    • 0038390881 scopus 로고    scopus 로고
    • Enzymatic desymmetrization of meso Cis-2,6-and Cis,Cis-2,4,6-substituted piperidines. Chemoenzymatic synthesis of (5S,9S)-(+)-indolizidine 209D
    • Chênevert, R., Mohammadi Ziarani, G., Morin, M. P., Dasser, M., Enzymatic Desymmetrization of meso Cis-2,6-and Cis,Cis-2,4,6-substituted piperidines. Chemoenzymatic Synthesis of (5S,9S)-(+)-Indolizidine 209D, Tetrahedron: Asymmetry, 10, p. 3117 (1999).
    • (1999) Tetrahedron: Asymmetry , vol.10 , pp. 3117
    • Chênevert, R.1    Mohammadi Ziarani, G.2    Morin, M.P.3    Dasser, M.4
  • 5
    • 0026770282 scopus 로고
    • Enzyme-catalyzed hydrolysis of N-benzyloxycarbonyl-cis-2,6- (acetoxymethyl) piperidine - A facile route to optically - Active piperidines
    • Chênevert, R. Dickman, M., Enzyme-Catalyzed Hydrolysis of N-Benzyloxycarbonyl-Cis-2,6-(Acetoxymethyl) Piperidine - A Facile Route to Optically - Active Piperidines, Tetrahedron: Asymm., 3, p. 1021 (1992).
    • (1992) Tetrahedron: Asymm. , vol.3 , pp. 1021
    • Chênevert, R.1    Dickman, M.2
  • 6
    • 0029953069 scopus 로고    scopus 로고
    • Enzymatic route to chiral, nonracemic cis-2,6- and cis, cis-2,4,6-substituted piperidines, synthesis of (+)-dihydropiridine and dendrobate alkaloid (+)-241 D
    • Chênevert, R., Dickman, M., Enzymatic Route to Chiral, nonracemic Cis-2,6- and Cis, Cis-2,4,6-Substituted Piperidines, Synthesis of (+)-dihydropiridine and dendrobate alkaloid (+)-241 D, J. Org. Chem., 61, p. 3332 (1996).
    • (1996) J. Org. Chem. , vol.61 , pp. 3332
    • Chênevert, R.1    Dickman, M.2
  • 7
    • 0001459139 scopus 로고
    • Asymmetric synthesis of indolizidines 167B and 223AB
    • Takahata, H., Bandoh, H., Momose, T., Asymmetric synthesis of indolizidines 167B and 223AB, Heterocycles, 41, 1797 (1995).
    • (1995) Heterocycles , vol.41 , pp. 1797
    • Takahata, H.1    Bandoh, H.2    Momose, T.3
  • 8
    • 0001367009 scopus 로고
    • Enantioselective Ru-mediated synthesis of (-)-indolizidine 223AB
    • Taber, D. F., Deker, P. B., Silverberg, L. J., Enantioselective Ru-mediated synthesis of (-)-indolizidine 223AB, J. Org. Chem., 57, p. 5990 (1992).
    • (1992) J. Org. Chem. , vol.57 , pp. 5990
    • Taber, D.F.1    Deker, P.B.2    Silverberg, L.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.