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Volumn 53, Issue 1, 2000, Pages 119-128

Bonaspectins and neobonaspectins, first sesquilignans and sesquineolignans from a convolvulaceous species

Author keywords

Bonamia spectabilis; Bonaspectin A; Bonaspectin B; Bonaspectin C 4'' glucoside; Bonaspectin D 4'' glucoside; Convolvulaceae; Lignan; Neobonaspectin A; Neobonaspectin B; Rel (7S,8S,7'R,8'R) 3,3',4,4',5,5' Hexamethoxy 7.O.7',8.8' lignan; Sesquilignans; Sesquineolignans

Indexed keywords

FURAN DERIVATIVE; LIGNAN; LIGNAN DERIVATIVE; MEDICINAL PLANT; TETRAHYDROFURAN;

EID: 0033959057     PISSN: 00319422     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0031-9422(99)00419-7     Document Type: Article
Times cited : (20)

References (34)
  • 4
    • 18844437321 scopus 로고
    • On the isolation, structure and properties of a new lignin from Humbertia madagascariensis
    • Combes, G., Billet, D., & Mentzer, C. (1959). On the isolation, structure and properties of a new lignin from Humbertia madagascariensis. Bulletin de la Societe Chimique de France, 2014.
    • (1959) Bulletin de la Societe Chimique de France , pp. 2014
    • Combes, G.1    Billet, D.2    Mentzer, C.3
  • 6
    • 0000364576 scopus 로고
    • 13C nuclear magnetic resonance spectral and conformational analysis of naturally occurring tetrahydrofuran lignans
    • 13C nuclear magnetic resonance spectral and conformational analysis of naturally occurring tetrahydrofuran lignans. Canadian Journal of Chemistry. 57:1979;441.
    • (1979) Canadian Journal of Chemistry , vol.57 , pp. 441
    • Fonseca, S.F.1    Barata, L.E.S.2    Ruveda, E.A.3
  • 8
    • 0343398793 scopus 로고
    • Extraktives of Chosenia arbutifolia A. Skvortz. I. Neolignans from the wood of Chosenia arbutifolia
    • Hashimoto Y., Ozawa S., Sasaya T. Extraktives of Chosenia arbutifolia A. Skvortz. I. Neolignans from the wood of Chosenia arbutifolia. Mokuzai Gakkaishi. 39:1993;1439.
    • (1993) Mokuzai Gakkaishi , vol.39 , pp. 1439
    • Hashimoto, Y.1    Ozawa, S.2    Sasaya, T.3
  • 11
    • 0028253744 scopus 로고
    • Jacpaniculines, the first lignanamides from the Convolvulaceae
    • Henrici A., Kaloga M., Eich E. Jacpaniculines, the first lignanamides from the Convolvulaceae. Phytochemistry. 37:1994;1637.
    • (1994) Phytochemistry , vol.37 , pp. 1637
    • Henrici, A.1    Kaloga, M.2    Eich, E.3
  • 12
    • 0027132692 scopus 로고
    • Accumulation of phenylpropanoids in the cotyledons of Morning Glory (Pharbitis nil) seedlings during the induction of flowering by poor nutrition
    • Hirai N., Kojima Y., Koshimizu K., Shinozaki M., Takimoto A. Accumulation of phenylpropanoids in the cotyledons of Morning Glory (Pharbitis nil) seedlings during the induction of flowering by poor nutrition. Plant and Cell Physiology. 34:1993;1039.
    • (1993) Plant and Cell Physiology , vol.34 , pp. 1039
    • Hirai, N.1    Kojima, Y.2    Koshimizu, K.3    Shinozaki, M.4    Takimoto, A.5
  • 13
    • 0027947799 scopus 로고
    • Accumulation of phenylpropanoids in cotyledons of Morning Glory (Pharbitis nil) seedlings during the induction of flowering by low temperature treatment, and the effect of precedent exposure to high-intensity light
    • Hirai N., Yamamuro M., Koshimizu K., Shinozaki M., Takimoto A. Accumulation of phenylpropanoids in cotyledons of Morning Glory (Pharbitis nil) seedlings during the induction of flowering by low temperature treatment, and the effect of precedent exposure to high-intensity light. Plant and Cell Physiology. 35:1994;691.
    • (1994) Plant and Cell Physiology , vol.35 , pp. 691
    • Hirai, N.1    Yamamuro, M.2    Koshimizu, K.3    Shinozaki, M.4    Takimoto, A.5
  • 14
    • 0001649490 scopus 로고
    • Lignans and neolignans from Buddleja davidii
    • Houghton P.J. Lignans and neolignans from Buddleja davidii. Phytochemistry. 24:1985;819.
    • (1985) Phytochemistry , vol.24 , pp. 819
    • Houghton, P.J.1
  • 15
    • 13444272646 scopus 로고    scopus 로고
    • Phytochemische Untersuchungen an Windengewächsen der Gattungen Calystegia, Convolvulus
    • Dissertation, Fachbereich Pharmazie, Freie Universität Berlin, Germany
    • Jenett-Siems, K. (1996). Phytochemische Untersuchungen an Windengewächsen der Gattungen Calystegia, Convolvulus, Ipomoea und Merremia unter besonderer Berücksichtigung des Alkaloidvorkommens. Dissertation, Fachbereich Pharmazie, Freie Universität Berlin, Germany.
    • (1996) Ipomoea und Merremia Unter Besonderer Berücksichtigung des Alkaloidvorkommens
    • Jenett-Siems, K.1
  • 21
    • 0343398789 scopus 로고
    • Structures of new lignans from Larix leptolepsis Gord
    • Miki, K., Sasaya, T., & Sakakibara, A. (1979). Structures of new lignans from Larix leptolepsis Gord. Tetrahedron Letters, 20, 799.
    • (1979) Tetrahedron Letters , vol.20 , pp. 799
    • Miki, K.1    Sasaya, T.2    Sakakibara, A.3
  • 22
    • 0343834493 scopus 로고
    • The mass spectra of oxygen heterocycles (III), an examination of simple lignans
    • Pelter A., Stainton A.P., Barber M. The mass spectra of oxygen heterocycles (III), an examination of simple lignans. Journal of Heterocyclic Chemistry. 3:1966;191.
    • (1966) Journal of Heterocyclic Chemistry , vol.3 , pp. 191
    • Pelter, A.1    Stainton, A.P.2    Barber, M.3
  • 23
    • 0000936041 scopus 로고
    • Manassantins A/B and saucerneol: Novel biologically active lignoids from Saururus cernuus
    • Rao K.V., Alvarez F.M. Manassantins A/B and saucerneol: novel biologically active lignoids from Saururus cernuus. Tetrahedron Letters. 24:1983;4947.
    • (1983) Tetrahedron Letters , vol.24 , pp. 4947
    • Rao, K.V.1    Alvarez, F.M.2
  • 24
    • 0001307933 scopus 로고
    • PMR analysis and conformation of 2,5-bis-(3,4,5-trimethoxyphenyl)-3,4-dimethyltetrahydrofuran isomers
    • Sarkanen K.V., Wallis A.F.A. PMR analysis and conformation of 2,5-bis-(3,4,5-trimethoxyphenyl)-3,4-dimethyltetrahydrofuran isomers. Journal of Heterocyclic Chemistry. 10:1973;1025.
    • (1973) Journal of Heterocyclic Chemistry , vol.10 , pp. 1025
    • Sarkanen, K.V.1    Wallis, A.F.A.2
  • 28
    • 0000274660 scopus 로고
    • Cytostatic activities of lignanolides from Ipomoea cairica
    • Trumm S., Eich E. Cytostatic activities of lignanolides from Ipomoea cairica. Planta Medica. 55:1989;658.
    • (1989) Planta Medica , vol.55 , pp. 658
    • Trumm, S.1    Eich, E.2
  • 30
    • 0030953722 scopus 로고    scopus 로고
    • Woorenol, a novel sesquineolignan with a unique spiro skeleton from the rhizomes of Coptis japonica var. dissecta
    • Yoshikawa K., Kinoshita H., Arihara S. Woorenol, a novel sesquineolignan with a unique spiro skeleton from the rhizomes of Coptis japonica var. dissecta. Journal of Natural Products. 60:1997;511.
    • (1997) Journal of Natural Products , vol.60 , pp. 511
    • Yoshikawa, K.1    Kinoshita, H.2    Arihara, S.3
  • 32
    • 0028334485 scopus 로고
    • Enantioselective route to threo 8.O.4′-type neolignans: Synthesis of (-)-virolin
    • Zacchino S.A. Enantioselective route to threo 8.O.4′-type neolignans: synthesis of (-)-virolin. Journal of Natural Products. 57:1994;446.
    • (1994) Journal of Natural Products , vol.57 , pp. 446
    • Zacchino, S.A.1
  • 33
    • 0022356095 scopus 로고
    • Stereoselective synthesis of 8.O.4′ neolignans: (±)-surinamensin and (±)-virolin
    • Zacchino S.A., Badano H. Stereoselective synthesis of 8.O.4′ neolignans: (±)-surinamensin and (±)-virolin. Journal of Natural Products. 48:1985;830.
    • (1985) Journal of Natural Products , vol.48 , pp. 830
    • Zacchino, S.A.1    Badano, H.2
  • 34
    • 33845279045 scopus 로고
    • Enantioselective synthesis and absolute configuration assignment of erythro-(3,4,5-trimethoxy-7-hydroxy-1′-allyl-2′,6′-dimethoxy)- 8.O.4′-neolignan, isolated from mace (Myristica fragrans)
    • Zacchino S.A., Badano H. Enantioselective synthesis and absolute configuration assignment of erythro-(3,4,5-trimethoxy-7-hydroxy-1′-allyl-2′,6′-dimethoxy)- 8.O.4′-neolignan, isolated from mace (Myristica fragrans). Journal of Natural Products. 51:1988;1261.
    • (1988) Journal of Natural Products , vol.51 , pp. 1261
    • Zacchino, S.A.1    Badano, H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.