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Volumn 56, Issue 12, 2000, Pages 1745-1757

New trimethylenemethane dianion synthons: Application to the preparation of substituted perhydrofuro[2,3-b]furans

Author keywords

Arene catalysis; Dianion synthons; Lithium; Perhydrofurofurans

Indexed keywords

1 OXACYCLOHEXANE 4,2' PERHYDROFURO[2,3 B]FURAN 5',4'' 1'' OXACYCLOHEXANE; 2 (TERT BUTYL) 5,5 DIETHYL 2 METHYLPERHYDROFURO[2,3 B]FURAN; 2 PHENYL 2 METHYLPERHYDROFURO[2,3 B]FURAN 5 1' CYCLOHEXANE; 2,2 DI(TERT BUTYL) 5,5 DIETHYLPERHYDROFURO[2,3 B]FURAN; 2,2 DIETHYL 5,5 DIMETHYLPERHYDROFURO[2,3 B]FURAN; 2,2,5,5 TETRACYCLOHEXYLPERHYDROFURO[2,3 B]FURAN; 2,2,5,5 TETRAETHYLPERHYDROFURO[2,3 B]FURAN; 2,2,5,5 TETRAMETHYLPERHYDROFURO[2,3 B]FURAN; 2,5 DI(TERT BUTYL) 2,5 DIMETHYLPERHYDROFURO[2,3 B]FURAN; 2,5 DI(TERT BUTYL)PERHYDROFURO[2,3 B]FURAN; 2,5 DIISOPROPYLPERHYDROFURO[2,3 B]FURAN; 2,5 DIMETHYL 2,5 DIPHENYLPERHYDROFURO[2,3 B]FURAN; 5 (TERT BUTYL) 2,2 DIETHYLPERHYDROFURO[2,3 B]FURAN; CYCLOHEXANE 1,2' PERHYDROFURO[2,3 B]FURAN 5',1'' CYCLOHEXANE; CYCLOHEXANE 1,2' PERHYDROFURO[2,3 B]FURAN 5',4'' 1'' OXACYCLOHEXANE; CYCLOPROPANE DERIVATIVE; FURAN DERIVATIVE; TRIMETHYLENEMETHANE; UNCLASSIFIED DRUG;

EID: 0034678137     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(00)00060-0     Document Type: Article
Times cited : (43)

References (69)
  • 7
    • 0002639152 scopus 로고
    • For reviews, see: (a)
    • For reviews, see: (a) Schuda, P. Top. Curr. Chem. 1980, 91, 75-111.
    • (1980) Top. Curr. Chem. , vol.91 , pp. 75-111
    • Schuda, P.1
  • 9
    • 53849086715 scopus 로고    scopus 로고
    • (c) Barton, D., Nakanishi, K., Meth-Cohn, D., Sankawa, V., Eds.; Elsevier: Oxford, Chapter 1.17
    • (c) Townsed, C. A.; Minto, R. E. In Comprehensive Natural Products Chemistry; Barton, D., Nakanishi, K., Meth-Cohn, D., Sankawa, V., Eds.; Elsevier: Oxford, 1999; Vol. 1, Chapter 1.17.
    • (1999) Comprehensive Natural Products Chemistry , vol.1
    • Townsed, C.A.1    Minto, R.E.2
  • 18
    • 0000613334 scopus 로고
    • C. 2nd ed. Searle. Washington, DC: American Chemical Society
    • Busby W.F. Jr., Wogan G.N. Searle C., 2nd ed. Chemical Carcinogens. Vol. 182:1984;945-1136 American Chemical Society, Washington, DC.
    • (1984) Chemical Carcinogens , vol.182 , pp. 945-1136
    • Busby W.F., Jr.1    Wogan, G.N.2
  • 19
    • 0011244444 scopus 로고
    • Council for Agricultural Science and Technology: Ames, (taken from Ref. 2h)
    • MycotoxinsEconomic and Health Risks, Council for Agricultural Science and Technology: Ames, 1988 (taken from Ref. 2h).
    • (1988) MycotoxinsEconomic and Health Risks
  • 21
    • 0033553112 scopus 로고    scopus 로고
    • Tin-promoted cyclisation
    • (a)
    • (a) Tin-promoted cyclisation: Trost, B.; Toste, F. D. J. Am. Chem. Soc. 1999, 121, 3543-3544.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 3543-3544
    • Trost, B.1    Toste, F.D.2
  • 32
  • 36
    • 0010688327 scopus 로고
    • M.J.S. Dewar, J.D. Dunitz, K. Hafner, E. Heilbronner, S. Ito, J.-M. Lehn, K. Niedenzu, K.N. Raymond, C.W. Rees, F. Vögtle, & G. Wittig. Berlin: Springer
    • Maerker A., Theis M. Dewar M.J.S., Dunitz J.D., Hafner K., Heilbronner E., Ito S., Lehn J.-M., Niedenzu K., Raymond K.N., Rees C.W., Vögtle F., Wittig G., Topics in Current Chemistry. Vol. 138:1987;18 Springer, Berlin.
    • (1987) Topics in Current Chemistry , vol.138 , pp. 18
    • Maerker, A.1    Theis, M.2
  • 54
    • 0030496093 scopus 로고    scopus 로고
    • For reviews, see: (a) Yus, M. Chem. Soc. Rev. 1996, 155-161.
    • (1996) Chem. Soc. Rev. , pp. 155-161
    • Yus, M.1
  • 56
    • 0033538083 scopus 로고    scopus 로고
    • Previous paper from our laboratory on this topic
    • Previous paper from our laboratory on this topic: Ortiz, J.; Guijarro, A.; Yus, M. Tetrahedron 1999, 55, 4831-4842.
    • (1999) Tetrahedron , vol.55 , pp. 4831-4842
    • Ortiz, J.1    Guijarro, A.2    Yus, M.3
  • 59
    • 0033520272 scopus 로고    scopus 로고
    • Organolithium from non-halogenated materials
    • Previous papers on the use of this methodology to prepare: (a) Organolithium from non-halogenated materials: Alonso, E.; Guijarro, D.; Martínez, P.; Ramón, D. J.; Yus, M. Tetrahedron 1999, 55, 11027-11038. For a review, see: Guijarro, D.; Yus, M. Recent Res. Devel. Org. Chem. 1998, 2, 713-744.
    • (1999) Tetrahedron , vol.55 , pp. 11027-11038
    • Alonso, E.1    Guijarro, D.2    Martínez, P.3    Ramón, D.J.4    Yus, M.5
  • 60
    • 0033520272 scopus 로고    scopus 로고
    • Previous papers on the use of this methodology to prepare: (a) Organolithium from non-halogenated materials
    • Previous papers on the use of this methodology to prepare: (a) Organolithium from non-halogenated materials: Alonso, E.; Guijarro, D.; Martínez, P.; Ramón, D. J.; Yus, M. Tetrahedron 1999, 55, 11027-11038. For a review, see: Guijarro, D.; Yus, M. Recent Res. Devel. Org. Chem. 1998, 2, 713-744.
    • (1998) Recent Res. Devel. Org. Chem. , vol.2 , pp. 713-744
    • Guijarro, D.1    Yus, M.2
  • 61
    • 0000084040 scopus 로고
    • Functionalised organolithium compounds
    • (b) Functionalised organolithium compounds: Ref. 26. For reviews, see
    • (b) Functionalised organolithium compounds: Ref. 26. For reviews, see: Nájera, C.; Yus, M. Trends Org. Chem. 1991, 1, 155-181. Nájera, C.; Yus, M. Recent Res. Devel. Org. Chem. 1997, 1, 67-96; Yus, M.; Foubelo, F. Rev. Heteroatom Chem. 1997, 17, 73-107.
    • (1991) Trends Org. Chem. , vol.1 , pp. 155-181
    • Nájera, C.1    Yus, M.2
  • 62
    • 0002333636 scopus 로고    scopus 로고
    • (b) Functionalised organolithium compounds: Ref. 26. For reviews, see
    • (b) Functionalised organolithium compounds: Ref. 26. For reviews, see: Nájera, C.; Yus, M. Trends Org. Chem. 1991, 1, 155-181. Nájera, C.; Yus, M. Recent Res. Devel. Org. Chem. 1997, 1, 67-96; Yus, M.; Foubelo, F. Rev. Heteroatom Chem. 1997, 17, 73-107.
    • (1997) Recent Res. Devel. Org. Chem. , vol.1 , pp. 67-96
    • Nájera, C.1    Yus, M.2
  • 63
    • 0001820427 scopus 로고    scopus 로고
    • (b) Functionalised organolithium compounds: Ref. 26. For reviews, see: Nájera, C.; Yus, M. Trends Org. Chem. 1991, 1, 155-181. Nájera, C.; Yus, M. Recent Res. Devel. Org. Chem. 1997, 1, 67-96; Yus, M.; Foubelo, F. Rev. Heteroatom Chem. 1997, 17, 73-107.
    • (1997) Rev. Heteroatom Chem. , vol.17 , pp. 73-107
    • Yus, M.1    Foubelo, F.2
  • 64
    • 0033593315 scopus 로고    scopus 로고
    • Polylithium synthons
    • (c) Polylithium synthons
    • (c) Polylithium synthons: Foubelo, F.; Yus, M. Tetrahedron Lett. 1999, 40, 743-746. For a review, see: Foubelo, F.; Yus, M. Trends Org. Chem. 1998, 7, 1-26.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 743-746
    • Foubelo, F.1    Yus, M.2
  • 65
    • 0033593315 scopus 로고    scopus 로고
    • For a review, see
    • (c) Polylithium synthons: Foubelo, F.; Yus, M. Tetrahedron Lett. 1999, 40, 743-746. For a review, see: Foubelo, F.; Yus, M. Trends Org. Chem. 1998, 7, 1-26.
    • (1998) Trends Org. Chem. , vol.7 , pp. 1-26
    • Foubelo, F.1    Yus, M.2
  • 66
    • 0031585040 scopus 로고    scopus 로고
    • Preliminary communications
    • Preliminary communications: (a)
    • Preliminary communications: (a) Alonso, F.; Lorenzo, E.; Yus, M. Tetrahedron Lett. 1997, 38, 2187-2190.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 2187-2190
    • Alonso, F.1    Lorenzo, E.2    Yus, M.3
  • 68
    • 0001196497 scopus 로고
    • This compound, which is commercially available (Aldrich), can be easily prepared from pentaerythriol
    • This compound, which is commercially available (Aldrich), can be easily prepared from pentaerythriol: Mondanaro-Lynch, K.; Dailey, W. P. J. Org. Chem. 1995, 60, 4666-4668.
    • (1995) J. Org. Chem. , vol.60 , pp. 4666-4668
    • Mondanaro-Lynch, K.1    Dailey, W.P.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.