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Volumn 15, Issue 4, 2004, Pages 647-652

Asymmetric synthesis of cyclopentenones with benzylic α-quaternary carbon stereogenic centres from furans

Author keywords

Cyclopentenones; Furans; Quaternary stereocentres

Indexed keywords

CARBON; CYCLOPENTENONE DERIVATIVE; FURAN DERIVATIVE;

EID: 1042298826     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetasy.2004.01.008     Document Type: Article
Times cited : (12)

References (36)
  • 1
    • 0003987170 scopus 로고
    • For some recent methods for the synthesis of optically active cyclopentanoids see: Weinheim: VCH
    • For some recent methods for the synthesis of optically active cyclopentanoids see: Ho T.-L. Carbocyclic Construction in Terpene Synthesis. 1988;VCH, Weinheim.
    • (1988) Carbocyclic Construction in Terpene Synthesis
    • Ho, T.-L.1
  • 18
    • 0037163335 scopus 로고    scopus 로고
    • For the stereoselective synthesis of other α-disubstituted cyclopentanones, see for example: and references cited therein
    • For the stereoselective synthesis of other α-disubstituted cyclopentanones, see for example: Yoshida M., Sugimoto K., Ihara M. Tetrahedron. 58:2000;7839. and references cited therein.
    • (2000) Tetrahedron , vol.58 , pp. 7839
    • Yoshida, M.1    Sugimoto, K.2    Ihara, M.3
  • 26
    • 0000780226 scopus 로고
    • The assignment of the absolute stereochemistries in the resolution step was based on the well-known ability of lipases to catalyse the acylation of the (R)-enantiomer of 2-substituted 4-hydroxycyclopent-2-enones. See for example:
    • The assignment of the absolute stereochemistries in the resolution step was based on the well-known ability of lipases to catalyse the acylation of the (R)-enantiomer of 2-substituted 4-hydroxycyclopent-2-enones. See for example: Babiak K.A., Ng J.S., Dygos J.H., Weyker C.L., Wang Y.-F., Wong C.-H. J. Org. Chem. 55:1990;3377.
    • (1990) J. Org. Chem. , vol.55 , pp. 3377
    • Babiak, K.A.1    Ng, J.S.2    Dygos, J.H.3    Weyker, C.L.4    Wang, Y.-F.5    Wong, C.-H.6
  • 27
    • 0020163034 scopus 로고
    • For the use of 4-hydroxycyclopent-2-enones as intermediates in the synthesis of prostaglandins see:
    • For the use of 4-hydroxycyclopent-2-enones as intermediates in the synthesis of prostaglandins see: Harre M., Raddatz P., Walenta R., Winterfeld E. Angew. Chem., Int. Ed. Engl. 21:1982;480.
    • (1982) Angew. Chem., Int. Ed. Engl. , vol.21 , pp. 480
    • Harre, M.1    Raddatz, P.2    Walenta, R.3    Winterfeld, E.4
  • 29
    • 0000784502 scopus 로고
    • For some other recent examples of the synthetic utility of 4-hydroxycyclopent-2-enones see:
    • For some other recent examples of the synthetic utility of 4-hydroxycyclopent-2-enones see: West F.G., Gunawardena G.U. J. Org. Chem. 58:1993;2402.
    • (1993) J. Org. Chem. , vol.58 , pp. 2402
    • West, F.G.1    Gunawardena, G.U.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.