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Volumn 44, Issue 3, 1998, Pages 244-246

Formation of optically active neolignans from achiral coniferyl alcohol by cell-free extracts of Eucommia ulmoides

Author keywords

Biosynthesis; Eucommia ulmoides; Guaiacylglycerol coniferyl ether; Lignan; Neolignan

Indexed keywords


EID: 0142129005     PISSN: 14350211     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF00521971     Document Type: Article
Times cited : (12)

References (10)
  • 1
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    • On the stereo selective synthesis of (+)-pinoresinol in Forsythia suspensa from its achiral precursor, coniferyl alcohol
    • Davin LB, Bedgar DL, Katayama T, Lewis NG (1992) On the stereo selective synthesis of (+)-pinoresinol in Forsythia suspensa from its achiral precursor, coniferyl alcohol. Phytochemistry 31:3869-3874
    • (1992) Phytochemistry , vol.31 , pp. 3869-3874
    • Davin, L.B.1    Bedgar, D.L.2    Katayama, T.3    Lewis, N.G.4
  • 2
    • 0028227564 scopus 로고
    • (+)-Pinoresinol synthase: A stereoselective oxidase catalysing 8,8′-lignan formation in Forsythia intermedia
    • Paré PW, Wang H-B, Davin LB, Lewis NG (1994) (+)-Pinoresinol synthase: a stereoselective oxidase catalysing 8,8′-lignan formation in Forsythia intermedia. Tetrahedron Lett 35:4731-4734
    • (1994) Tetrahedron Lett , vol.35 , pp. 4731-4734
    • Paré, P.W.1    Wang, H.-B.2    Davin, L.B.3    Lewis, N.G.4
  • 3
    • 0031031957 scopus 로고    scopus 로고
    • Stereoselective bimolecular phenoxy radical coupling by an auxiliary (dirigent) protein without an active center
    • Davin LB, Wang H-B, Crowell AL, Bedgar DL, Martin DM, Sarkanen S, Lewis NG (1997) Stereoselective bimolecular phenoxy radical coupling by an auxiliary (dirigent) protein without an active center. Science 275:362-366
    • (1997) Science , vol.275 , pp. 362-366
    • Davin, L.B.1    Wang, H.-B.2    Crowell, A.L.3    Bedgar, D.L.4    Martin, D.M.5    Sarkanen, S.6    Lewis, N.G.7
  • 4
    • 85016994417 scopus 로고
    • The constituents of Eucommia ulmoides Oliv. V. Isolation of dihydroxydehy-drodiconiferyl alcohol isomers and phenolic compounds
    • Deyama T, Ikawa T, Kitagawa S, Nishibe S (1987) The constituents of Eucommia ulmoides Oliv. V. Isolation of dihydroxydehy-drodiconiferyl alcohol isomers and phenolic compounds. Chem Pharm Bull (Tokyo) 35:1785-1789
    • (1987) Chem Pharm Bull (Tokyo) , vol.35 , pp. 1785-1789
    • Deyama, T.1    Ikawa, T.2    Kitagawa, S.3    Nishibe, S.4
  • 5
    • 85016963622 scopus 로고
    • The constituents of Eucommia ulmoides Oliv. VI. Isolation of a new sesquilignan and neolignan glycosides
    • Deyama T, Ikawa T, Kitagawa S, Nishibe S (1987) The constituents of Eucommia ulmoides Oliv. VI. Isolation of a new sesquilignan and neolignan glycosides. Chem Pharm Bull (Tokyo) 35:1803-1807
    • (1987) Chem Pharm Bull (Tokyo) , vol.35 , pp. 1803-1807
    • Deyama, T.1    Ikawa, T.2    Kitagawa, S.3    Nishibe, S.4
  • 6
    • 0026955965 scopus 로고
    • An extraordinary accumulation of (-)-pinoresinol in cell-free extracts of Forsythia intermedia: Evidence for enantiospecific reduction of (+)-pinoresinol
    • Katayama T, Davin LB, Lewis NG (1992) An extraordinary accumulation of (-)-pinoresinol in cell-free extracts of Forsythia intermedia: evidence for enantiospecific reduction of (+)-pinoresinol. Phytochemistry 31:3875-3881
    • (1992) Phytochemistry , vol.31 , pp. 3875-3881
    • Katayama, T.1    Davin, L.B.2    Lewis, N.G.3
  • 7
    • 0017184389 scopus 로고
    • A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding
    • Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Chem 72:248-252
    • (1976) Anal Chem , vol.72 , pp. 248-252
    • Bradford, M.M.1
  • 8
    • 0000141137 scopus 로고    scopus 로고
    • Biosynthesis and stereochemistry of lignans in Zanthoxylum ailanthoides. I. (+)-Lariciresinol formation by enzymatic reduction of (±)-pinoresinols
    • Katayama T, Masaoka T, Yamada H (1997) Biosynthesis and stereochemistry of lignans in Zanthoxylum ailanthoides. I. (+)-Lariciresinol formation by enzymatic reduction of (±)-pinoresinols. Mokuzai Gakkaishi 43:580-588
    • (1997) Mokuzai Gakkaishi , vol.43 , pp. 580-588
    • Katayama, T.1    Masaoka, T.2    Yamada, H.3
  • 10
    • 0003099323 scopus 로고
    • Biosynthesis of dehydrodiconiferyl alcohol glucosides: Implications for the control of tobacco cell growth
    • Orr JD, Lynn DG (1992) Biosynthesis of dehydrodiconiferyl alcohol glucosides: implications for the control of tobacco cell growth. Plant Physiol 98:343-352
    • (1992) Plant Physiol , vol.98 , pp. 343-352
    • Orr, J.D.1    Lynn, D.G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.