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Volumn 23, Issue 7, 2009, Pages 665-671

A p-quinol isoflavan and two new isoflavanones from Desmodium canum

Author keywords

Desmodium canum; Isoflavanones; Oxygen heterocycles; p quinol isoflavan; Prenylated isoflavonoids

Indexed keywords

DESMODIANONE D; DESMODIANONE F; DESMODIANONE G; DESMODIUM CANUM EXTRACT; ISOFLAVAN DERIVATIVE; ISOFLAVONOID; PLANT EXTRACT; UNCLASSIFIED DRUG; ISOFLAVONE DERIVATIVE;

EID: 67049160333     PISSN: 14786419     EISSN: 14786427     Source Type: Journal    
DOI: 10.1080/14786410802362717     Document Type: Article
Times cited : (12)

References (8)
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    • (2003) Phytochemistry , vol.64 , pp. 599-602
    • Botta, B.1    Gacs-Baitz, E.2    Vinciguerra, V.3    Delle Monache, G.4
  • 2
    • 33746211332 scopus 로고    scopus 로고
    • Oxidative de-aromatization of para-alkyl phenols into para-peroxyquinols and para-quinols mediated by oxone as a source of singlet oxygen
    • DOI 10.1002/anie.200504605
    • Carreño, M.C., González-López, M., & Urbano, A. (2006). Oxidative de-aromatization of para-alkyl phenols into para-peroxyquinols and para-quinols mediated by oxone as a source of singlet oxygen. Angewandte Chemie (International Ed., in English), 45, 2737-2741. (Pubitemid 44099095)
    • (2006) Angewandte Chemie - International Edition , vol.45 , Issue.17 , pp. 2737-2741
    • Carreno, M.C.1    Gonzalez-Lopez, M.2    Urbano, A.3
  • 4
    • 0000530381 scopus 로고
    • Biogenesis-like transformation of salidroside to rengyol and its related cyclohexyletanoids of Forsythia suspensa
    • Endo, K., Seya, K., & Hikino, H. (1989). Biogenesis-like transformation of salidroside to rengyol and its related cyclohexyletanoids of Forsythia suspensa. Tetrahedron, 45, 3673-3682.
    • (1989) Tetrahedron , vol.45 , pp. 3673-3682
    • Endo, K.1    Seya, K.2    Hikino, H.3
  • 5
    • 0000029584 scopus 로고
    • The mass spectra of oxygen heterocycles. II. The mass spectra of some flavonoids
    • Pelter, A., Stainton, P., & Barber, M. (1965). The mass spectra of oxygen heterocycles. II. The mass spectra of some flavonoids. Journal of Heterocyclic Chemistry, 2, 262-271.
    • (1965) Journal of Heterocyclic Chemistry , vol.2 , pp. 262-271
    • Pelter, A.1    Stainton, P.2    Barber, M.3
  • 6
    • 0033821244 scopus 로고    scopus 로고
    • Halleridone and Hallerone from Phyla nodiflora as taxonomic markers
    • DOI 10.1016/S0305-1978(00)00007-7, PII S0305197800000077
    • Ravikanth, V., Ramesh, P., Diwan, P.V., & Yenkateswarlu, Y. (2000). Halleridone and hallerone from Phyla nodiflora as taxonomic markers. Biochemical Systematics and Ecology, 28, 905-906. (Pubitemid 30687999)
    • (2000) Biochemical Systematics and Ecology , vol.28 , Issue.9 , pp. 905-906
    • Ravikanth, V.1    Ramesh, P.2    Diwan, P.V.3    Venkateswarlu, Y.4
  • 8
    • 24344451200 scopus 로고    scopus 로고
    • Circular dichroism, a powerful tool for the assessment of absolute configuration of flavonoids
    • DOI 10.1016/j.phytochem.2005.02.002, PII S0031942205000531
    • Slade, D., Ferreira, D., & Marais, J.P.J. (2005). Circular dichroism, a powerful tool for the assessment of absolute configuration of flavonoids. Phytochemistry, 66, 2177-2215. (Pubitemid 41254096)
    • (2005) Phytochemistry , vol.66 , Issue.18 SPEC. ISS , pp. 2177-2215
    • Slade, D.1    Ferreira, D.2    Marais, J.P.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.