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Volumn 43, Issue 45, 2002, Pages 8195-8199

An enantioselective total synthesis of phomopsolide C

Author keywords

[No Author keywords available]

Indexed keywords

LACTIC ACID; LACTONE DERIVATIVE; PHOMOPSOLIDE C; UNCLASSIFIED DRUG;

EID: 0037020583     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(02)01866-X     Document Type: Article
Times cited : (24)

References (28)
  • 8
    • 0035844707 scopus 로고    scopus 로고
    • For the application of this approach toward several styryllactone natural products see: (a) Harris, J. M.; O'Doherty, G. A. Tetrahedron 2001, 57, 5161-5171; (b) Harris, J. M.; O'Doherty, G. A. Org. Lett. 2000, 2, 2983-2986.
    • (2001) Tetrahedron , vol.57 , pp. 5161-5171
    • Harris, J.M.1    O'Doherty, G.A.2
  • 9
    • 0034699287 scopus 로고    scopus 로고
    • For the application of this approach toward several styryllactone natural products see: (a) Harris, J. M.; O'Doherty, G. A. Tetrahedron 2001, 57, 5161-5171; (b) Harris, J. M.; O'Doherty, G. A. Org. Lett. 2000, 2, 2983-2986.
    • (2000) Org. Lett. , vol.2 , pp. 2983-2986
    • Harris, J.M.1    O'Doherty, G.A.2
  • 12
    • 0035940146 scopus 로고    scopus 로고
    • For the synthesis of cryptocarya diacetate see: Hunter, T. J.; O'Doherty, G. A. Org. Lett. 2001, 3, 2777-2780.
    • (2001) Org. Lett. , vol.3 , pp. 2777-2780
    • Hunter, T.J.1    O'Doherty, G.A.2
  • 16
    • 0005223779 scopus 로고    scopus 로고
    • note
    • Stierle proposed the names E-phomopsolide A, 6,7-dihydro-phomopsolide B and 6,7-dihydrophomopsolide B for compounds 1c, 1d, 1e respectively, see Ref. 6. For simplicity sake, we have chosen to use the names phompsolide C, D, and E for the natural products 1c, 1d, 1e respectively.
  • 19
    • 0005129150 scopus 로고    scopus 로고
    • note
    • (a) An Achmatowicz reaction is the oxidative rearrangement of furfuryl alcohols to 2-substituted 6-hydroxy-2H-pyran-3(6H)-ones, see: Ref. 13;
  • 24
    • 0005196057 scopus 로고    scopus 로고
    • 13C NMR, FTIR, HRMS, and/or EA analysis.
    • 13C NMR, FTIR, HRMS, and/or EA analysis.
  • 25
    • 33947086629 scopus 로고
    • 19F NMR of the Mosher ester derivatives, see: (a) Sullivan, G. R.; Dale, J. A.; Mosher, H. S. J. Org. Chem. 1973, 38, 2143-2147; (b) Yamaguchi, S.; Yasuhara, F.; Kabuto, K. T. Tetrahedron 1976, 32, 1363-1367.
    • (1973) J. Org. Chem. , vol.38 , pp. 2143-2147
    • Sullivan, G.R.1    Dale, J.A.2    Mosher, H.S.3
  • 26
    • 0001384141 scopus 로고
    • 19F NMR of the Mosher ester derivatives, see: (a) Sullivan, G. R.; Dale, J. A.; Mosher, H. S. J. Org. Chem. 1973, 38, 2143-2147; (b) Yamaguchi, S.; Yasuhara, F.; Kabuto, K. T. Tetrahedron 1976, 32, 1363-1367.
    • (1976) Tetrahedron , vol.32 , pp. 1363-1367
    • Yamaguchi, S.1    Yasuhara, F.2    Kabuto, K.T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.