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Volumn 39, Issue 45, 1998, Pages 8335-8336

Synthesis of a protected derivative of (±)-1-(hydroxymethyl)conduritol C from 2-(hydroxymethyl)furan

Author keywords

[No Author keywords available]

Indexed keywords

1 (HYDROXYMETHYL)CONDURITOL C; 2 (HYDROXYMETHYL)FURAN; 7 OXANORBOMENIC SULFONE; FURAN DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0032487879     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)01936-4     Document Type: Article
Times cited : (12)

References (17)
  • 10
    • 0030845835 scopus 로고    scopus 로고
    • 3. For a recent review on the use of furan and derivatives in organic synthesis, see: Kappe, C. O.; Murphree, S. S.; Padwa, A.; Tetrahedron 1997, 57, 14179.
    • (1997) Tetrahedron , vol.57 , pp. 14179
    • Kappe, C.O.1    Murphree, S.S.2    Padwa, A.3
  • 11
    • 0032581607 scopus 로고    scopus 로고
    • 4. An experimental and theoretical study of the regioselectivity of the Diels-Alder cycloaddition of E-1,2-bis-(phenylsulfonyl)ethylene and some 2-substituted furans has been reported. See, Arjona, O.; Iradier, F.; Mañas, R. M.; Plumet, J.; Grabuleda X.; Jaime, C.; Tetrahedron 1998, 54, 9095-9110.
    • (1998) Tetrahedron , vol.54 , pp. 9095-9110
    • Arjona, O.1    Iradier, F.2    Mañas, R.M.3    Plumet, J.4    Grabuleda, X.5    Jaime, C.6
  • 13
    • 0003102932 scopus 로고    scopus 로고
    • 6. For selected and recent reviews on the ring opening of oxabicyclic compounds, see: a) Chiu, P.; Lautens, M.; Topics Curr. Chem. 1997, 790, 3.
    • (1997) Topics Curr. Chem. , vol.790 , pp. 3
    • Chiu, P.1    Lautens, M.2
  • 16
    • 0002865952 scopus 로고
    • b) Kocienski, P. J.; Chem. Ind. 1981, 548. The orientation of this elimination reaction can be accounted for considering the mechanism of the process. For a discussion on this point, see: Simpkins, N. G. in "Sulphones in Organic Synthesis" Tetrahedron Organic Chemistry Series, Vol. 10. Pergamon Press, 1993. Pp. 256-258.
    • (1981) Chem. Ind. , pp. 548
    • Kocienski, P.J.1
  • 17
    • 0004067242 scopus 로고
    • Pergamon Press
    • b) Kocienski, P. J.; Chem. Ind. 1981, 548. The orientation of this elimination reaction can be accounted for considering the mechanism of the process. For a discussion on this point, see: Simpkins, N. G. in "Sulphones in Organic Synthesis" Tetrahedron Organic Chemistry Series, Vol. 10. Pergamon Press, 1993. Pp. 256-258.
    • (1993) "Sulphones in Organic Synthesis" Tetrahedron Organic Chemistry Series , vol.10 , pp. 256-258
    • Simpkins, N.G.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.