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Flavan derivatives. XIV. The absolute configurations of some 1,2-diarylpropane derivatives and of some isoflavans

JW Clark-Lewis, I Dainis and GC Ramsay
18(7) pp.1035 - 1048


17 articles found in Crossref database.

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Gregson Michael, Ollis W.David, Redman Brian T., Sutherland Ian O., Dietrichs H.H., Gottlieb Otto R.
Phytochemistry. 1978 17(8). p.1395
Duartin, an isoflavan from Machaerium opacum
Ollis W.David, Sutherland Ian O., Alves Herbert M., Gottlieb Otto R.
Phytochemistry. 1978 17(8). p.1401
Stereoselective synthesis of isoflavonoids. (R)- and (S)-isoflavens
Versteeg Marietjie, Bezuidenhoudt Barend C.B., Ferreira Daneel
Tetrahedron. 1999 55(11). p.3365
Stereochemistry of 3-hydroxy- and 3-acetoxyflavanone oximes
Janzsó G., Kállay F., Koczor I., Radics L.
Tetrahedron. 1967 23(9). p.3699
Circular dichroism, a powerful tool for the assessment of absolute configuration of flavonoids
Slade Desmond, Ferreira Daneel, Marais Jannie P.J.
Phytochemistry. 2005 66(18). p.2177
Fortschritte der Chemie Organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products (1975)
Scopes P. M.
Phenolic neorautanenia isoflavanoids
Brink A.J., Rall G.J.H., Engelbrecht J.P.
Tetrahedron. 1974 30(2). p.311
Optically active aromatic chromophores—VIII
Verbit L., Clark-Lewis J.W.
Tetrahedron. 1968 24(16). p.5519
Atlas of Stereochemistry (1974)
Klyne W., Buckingham J.
Fortschritte der Chemie Organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products (1970)
Wong E.
Topics in Stereochemistry (1967)
Crabbé Pierre
Enantiomeric separation of substituted flavanoids by LC-DAD
Quaglia M.G., Desideri N., Bossù E., Melchiorre P., Conti C.
Journal of Pharmaceutical and Biomedical Analysis. 1991 9(10-12). p.811
Circular dichroism spectra of flavanols
Korver O., Wilkins C.K.
Tetrahedron. 1971 27(22). p.5459
Isoflavonoids of Dalbergia ecastophyllum
Donnelly Dervilla M.X., Keenan P.J., Prendergast J.P.
Phytochemistry. 1973 12(5). p.1157
Absolute configurations of isoflavans
Kurosawa Kazu, Ollis W.David, Redman Brian T., Sutherland Ian O., Alves Herbert M., Gottlieb Otto R.
Phytochemistry. 1978 17(8). p.1423
Optical rotatory dispersion and circular dichroism or aromatic compounds: a general survey
Crabbé P., Klyne W.
Tetrahedron. 1967 23(8). p.3449
S-Equol, a potent ligand for estrogen receptor β, is the exclusive enantiomeric form of the soy isoflavone metabolite produced by human intestinal bacterial flora1–4,
Setchell Kenneth DR, Clerici Carlo, Lephart Edwin D, Cole Sidney J, Heenan Claire, Castellani Danilo, Wolfe Brian E, Nechemias-Zimmer Linda, Brown Nadine M, Lund Trent D, Handa Robert J, Heubi James E
The American Journal of Clinical Nutrition. 2005 81(5). p.1072

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