메뉴 건너뛰기




Volumn 63, Issue 8, 2003, Pages 931-937

Two cyclohexenone glycosides from the North American fern Woodwardia virginica (L.) Smith

Author keywords

Blechnaceae; Cyclohexenone glucosides; North American fern; Woodwardia virginica

Indexed keywords

2 CYCLOHEXENONE; ALCOHOL; GLYCOSIDE;

EID: 0041519148     PISSN: 00319422     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0031-9422(03)00358-3     Document Type: Article
Times cited : (8)

References (31)
  • 1
    • 33845184916 scopus 로고
    • Novel sponge-derived amino acids. 5. Structures, stereochemistry, and synthesis of several new heterocycles
    • Adamczeski, M., Quinoa, E., Crews, P., 1989. Novel sponge-derived amino acids. 5. Structures, stereochemistry, and synthesis of several new heterocycles. J. Am. Chem. Soc. 111, 647-654.
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 647-654
    • Adamczeski, M.1    Quinoa, E.2    Crews, P.3
  • 2
    • 0031001806 scopus 로고    scopus 로고
    • Carvotacetone derivatives from the Egyptian plant Sphaeranthus suaveolens
    • Ahmed, A.A., Mahmoud, A.A., 1997. Carvotacetone derivatives from the Egyptian plant Sphaeranthus suaveolens. Phytochemistry 45, 533-535.
    • (1997) Phytochemistry , vol.45 , pp. 533-535
    • Ahmed, A.A.1    Mahmoud, A.A.2
  • 3
    • 0345311216 scopus 로고
    • Proton and carbon-13 assignments from sensitivity-enhanced detection of heteronuclear multiple-bond connectivity by 2D multiple quantum NMR
    • Bax, A., Summers. M.F., 1986. Proton and carbon-13 assignments from sensitivity-enhanced detection of heteronuclear multiple-bond connectivity by 2D multiple quantum NMR. J. Am. Chem. Soc. 108, 2093-2094.
    • (1986) J. Am. Chem. Soc. , vol.108 , pp. 2093-2094
    • Bax, A.1    Summers, M.F.2
  • 4
    • 49949140444 scopus 로고
    • Mass spectrometry of partially methylated alditol acetates
    • Björndal, H., Lindberg, B., Svensson, S., 1967. Mass spectrometry of partially methylated alditol acetates. Carbohydr. Res. 5, 433-440.
    • (1967) Carbohydr. Res. , vol.5 , pp. 433-440
    • Björndal, H.1    Lindberg, B.2    Svensson, S.3
  • 6
    • 37049045075 scopus 로고
    • The mechanism of the reaction of boron trichloride with cyclic acetals of hexitols
    • Bonner, T.G., Saville, N.M., 1960. The mechanism of the reaction of boron trichloride with cyclic acetals of hexitols. J. Chem. Soc., 1, 2851-2858.
    • (1960) J. Chem. Soc. , vol.1 , pp. 2851-2858
    • Bonner, T.G.1    Saville, N.M.2
  • 8
    • 0033570098 scopus 로고    scopus 로고
    • Pteridanoside, the first protoilludane sesquiterpene glucoside as a toxic component of the neotropical bracken fern Pteridium aquilinum var. caudatum
    • Castillio, U.F., Sakagami, Y., Alonso-Amelot, M., Ojika, M., 1999. Pteridanoside, the first protoilludane sesquiterpene glucoside as a toxic component of the neotropical bracken fern Pteridium aquilinum var. caudatum. Tetrahedron 55, 12295-12300.
    • (1999) Tetrahedron , vol.55 , pp. 12295-12300
    • Castillio, U.F.1    Sakagami, Y.2    Alonso-Amelot, M.3    Ojika, M.4
  • 10
    • 0043140825 scopus 로고
    • The carbohydrate units of ovalbumin: Complete structures of three glycopeptides. 1,3,4,5,6-penta-O-acetyl-2-O-methyl-D-glucitol
    • Conchie, J., Stracham, I., 1978. The carbohydrate units of ovalbumin: Complete structures of three glycopeptides. 1,3,4,5,6-penta-O-acetyl-2-O-methyl-D-glucitol. Carbohyd. Res. 63, 193-213.
    • (1978) Carbohyd. Res. , vol.63 , pp. 193-213
    • Conchie, J.1    Stracham, I.2
  • 11
    • 0000326683 scopus 로고
    • Determination of the D and L configuration of neutral monosaccharides by high-resolution capillary GLC
    • Gerwig, G.J., Kamerling, J.R., Vliegenthart, J.F.G., 1978. Determination of the D and L configuration of neutral monosaccharides by high-resolution capillary GLC. Carbohydr. Res. 62, 349-357.
    • (1978) Carbohydr. Res. , vol.62 , pp. 349-357
    • Gerwig, G.J.1    Kamerling, J.R.2    Vliegenthart, J.F.G.3
  • 13
    • 0041519148 scopus 로고    scopus 로고
    • A trinorsesterterpene glycoside from the North American fern Woodwardia virginica (L.) Smith
    • in press
    • Hanuš, L.O., Rezanka, T., Dembitsky, V.M., 2003. A trinorsesterterpene glycoside from the North American fern Woodwardia virginica (L.) Smith. Phytochemistry (in press).
    • (2003) Phytochemistry
    • Hanuš, L.O.1    Rezanka, T.2    Dembitsky, V.M.3
  • 14
    • 0013602337 scopus 로고
    • Carvotacetone derivatives and eudesman-12,6-beta-olides from Sphaeranthus species
    • Jakupovic, J., Grenz, M., Bohlmann, F., Mungai, G.M., 1990. Carvotacetone derivatives and eudesman-12,6-beta-olides from Sphaeranthus species. Phytochemistry 29, 1213-1217.
    • (1990) Phytochemistry , vol.29 , pp. 1213-1217
    • Jakupovic, J.1    Grenz, M.2    Bohlmann, F.3    Mungai, G.M.4
  • 15
    • 0032102981 scopus 로고    scopus 로고
    • Sesquiterpene glycosides and sesquilignan glycosides from stems of Alangium premnifolium
    • Kijima, K., Otsuka, H., Ide, T., Ogimi, C., Hirata, E., Takushi, A., Takeda, Y., 1998. Sesquiterpene glycosides and sesquilignan glycosides from stems of Alangium premnifolium. Phytochemistry 48, 669-676.
    • (1998) Phytochemistry , vol.48 , pp. 669-676
    • Kijima, K.1    Otsuka, H.2    Ide, T.3    Ogimi, C.4    Hirata, E.5    Takushi, A.6    Takeda, Y.7
  • 16
    • 0026066368 scopus 로고
    • Structure of isoferprenin, a 4-hydroxycoumarin derivative from Ferula communis var. genuine
    • Lamnaouer, D., Fraigui, O., Martin, M.T., Gallard, J.F., Bodo, B., 1991. Structure of isoferprenin, a 4-hydroxycoumarin derivative from Ferula communis var. genuine. J. Nat. Prod. 54, 576-578.
    • (1991) J. Nat. Prod. , vol.54 , pp. 576-578
    • Lamnaouer, D.1    Fraigui, O.2    Martin, M.T.3    Gallard, J.F.4    Bodo, B.5
  • 17
    • 37049081055 scopus 로고
    • Computation of vicinal coupling-constants in tetra-alditol and hexa-alditol peracetates using molecular mechanics - A rational approach to conformational analysis in solution
    • Masamune, S., Ma, P., Moore, R.E., Fujiyoshi, T., Jaime, C., Osawa, E., 1986. Computation of vicinal coupling-constants in tetra-alditol and hexa-alditol peracetates using molecular mechanics- a rational approach to conformational analysis in solution. J. Chem. Soc. Chem. Commun. 3, 261-263.
    • (1986) J. Chem. Soc. Chem. Commun. , vol.3 , pp. 261-263
    • Masamune, S.1    Ma, P.2    Moore, R.E.3    Fujiyoshi, T.4    Jaime, C.5    Osawa, E.6
  • 18
    • 0041637941 scopus 로고
    • Chemical-ionization mass spectrometry of methylated hexitol acetates
    • McNeil, M., Albersheim, P., 1977. Chemical-ionization mass spectrometry of methylated hexitol acetates. Carbohydr. Res. 56, 239-248.
    • (1977) Carbohydr. Res. , vol.56 , pp. 239-248
    • McNeil, M.1    Albersheim, P.2
  • 19
    • 38249021990 scopus 로고
    • Chemosystematics of di- and sesquiterpenoids in polypodiaceous ferns
    • Murakami, T., Saiki, Y., 1989. Chemosystematics of di- and sesquiterpenoids in polypodiaceous ferns. Biochem. Syst. Ecol. 17, 131-140.
    • (1989) Biochem. Syst. Ecol. , vol.17 , pp. 131-140
    • Murakami, T.1    Saiki, Y.2
  • 20
    • 2142858450 scopus 로고
    • High-field FT NMR application of Mosher method - The absolute-configurations of marine terpenoids
    • Ohtani, I., Kusumi, T., Kashman, Y., Kakisawa, H., 1991a. High-field FT NMR application of Mosher method - the absolute-configurations of marine terpenoids. J. Am. Chem. Soc. 113, 4092-4095.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 4092-4095
    • Ohtani, I.1    Kusumi, T.2    Kashman, Y.3    Kakisawa, H.4
  • 21
    • 33751500812 scopus 로고
    • A new aspect of the high-field NMR application of Mosher method - The absolute-configuration of marine triterpene sipholenol-A
    • Ohtani, I., Kusumi, T., Kashman, Y., Kakisawa, H., 1991b. A new aspect of the high-field NMR application of Mosher method - the absolute-configuration of marine triterpene sipholenol-A. J. Org. Chem. 56, 1296-1298.
    • (1991) J. Org. Chem. , vol.56 , pp. 1296-1298
    • Ohtani, I.1    Kusumi, T.2    Kashman, Y.3    Kakisawa, H.4
  • 22
    • 0025905744 scopus 로고
    • On the possibility of determining stereochemistry in acyclic polyhydroxylated compounds by the combined vicinal coupling-constant molecular mechanics method - A test with alditol peracetates
    • Osawa, E., Imai, K., Fujiyoshi, Y., Teruyo, Y., Carlos, J., Philip, M., Masamune, S., 1991. On the possibility of determining stereochemistry in acyclic polyhydroxylated compounds by the combined vicinal coupling-constant molecular mechanics method - a test with alditol peracetates. Tetrahedron 47, 4579-4590.
    • (1991) Tetrahedron , vol.47 , pp. 4579-4590
    • Osawa, E.1    Imai, K.2    Fujiyoshi, Y.3    Teruyo, Y.4    Carlos, J.5    Philip, M.6    Masamune, S.7
  • 23
    • 0034622537 scopus 로고    scopus 로고
    • Glycosidic compounds of murolic, protoconstipatic and allo-murolic acids from lichens of Central Asia
    • Řezanka, T., Guschina, I.A., 2000. Glycosidic compounds of murolic, protoconstipatic and allo-murolic acids from lichens of Central Asia. Phytochemistry 54, 635-645.
    • (2000) Phytochemistry , vol.54 , pp. 635-645
    • Řezanka, T.1    Guschina, I.A.2
  • 24
    • 37049109804 scopus 로고
    • C-13 nuclear magnetic-resonance spectra of acyclic carbohydrate-derivatives-alditols, 1,2-bis(phenylhydrazones), and dithioacetals
    • Schnarr, G.W., Vyas, D.M., Szarek, W.A., 1979. C-13 nuclear magnetic-resonance spectra of acyclic carbohydrate-derivatives-alditols, 1,2-bis(phenylhydrazones), and dithioacetals. J. Chem. Soc., Perkin Trans. I, 496-503.
    • (1979) J. Chem. Soc., Perkin Trans. I , pp. 496-503
    • Schnarr, G.W.1    Vyas, D.M.2    Szarek, W.A.3
  • 25
    • 0018663758 scopus 로고
    • Isoepoxydon, a new metabolite of the patulin pathway in Penicillium urticae
    • Sekiguchi, J., Gaucher, G.M., 1979. Isoepoxydon, a new metabolite of the patulin pathway in Penicillium urticae. Biochem. J. 182, 445-453.
    • (1979) Biochem. J. , vol.182 , pp. 445-453
    • Sekiguchi, J.1    Gaucher, G.M.2
  • 26
    • 0029933767 scopus 로고    scopus 로고
    • Ring conformational requirement for biological activity of abscisic acid probed by the cyclopropane analogues
    • Todoroki, Y., Nakano, S., Hirai, N., Ohigashi, H., 1996. Ring conformational requirement for biological activity of abscisic acid probed by the cyclopropane analogues. Tetrahedron 52, 8081-8098.
    • (1996) Tetrahedron , vol.52 , pp. 8081-8098
    • Todoroki, Y.1    Nakano, S.2    Hirai, N.3    Ohigashi, H.4
  • 27
    • 0000764027 scopus 로고
    • Glycosidation shifts in carbon-13 NMR spectroscopy: Carbon-13 signal shifts from aglycone and glucose to glucoside
    • Tori, K., Seo, S., Yoshimura, Y., Arita, H., Tomita, Y., 1977. Glycosidation shifts in carbon-13 NMR spectroscopy: carbon-13 signal shifts from aglycone and glucose to glucoside. Tetrahedron Lett. 1, 179-182.
    • (1977) Tetrahedron Lett. , vol.1 , pp. 179-182
    • Tori, K.1    Seo, S.2    Yoshimura, Y.3    Arita, H.4    Tomita, Y.5
  • 30
    • 0036898856 scopus 로고    scopus 로고
    • Immunomodulatory sesquiterpene glycosides from Dendrobium nobile
    • Ye, Q., Guowei Qin, G., Zhao, W., 2002. Immunomodulatory sesquiterpene glycosides from Dendrobium nobile. Phytochemistry 61, 885-890.
    • (2002) Phytochemistry , vol.61 , pp. 885-890
    • Ye, Q.1    Guowei Qin, G.2    Zhao, W.3
  • 31
    • 0007553786 scopus 로고
    • Carvotacetone derivatives and other constituents from representatives of the Sphaeranthus group
    • Zdero, C., Bohlmann, F., Mungai, G., 1991. Carvotacetone derivatives and other constituents from representatives of the Sphaeranthus group. Phytochemistry 30, 3297-3303.
    • (1991) Phytochemistry , vol.30 , pp. 3297-3303
    • Zdero, C.1    Bohlmann, F.2    Mungai, G.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.