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- Biosynthesis of isoflavonoid phytoalexins in Medicago sativa: the biosynthetic relationship between pterocarpans and 2′-hydroxyisoflavans. Paul M. Dewick, Maria Martin
, J. Chem. Soc., Chem. Commun.
, 1976
, 637
- Isoflavonoids of the Leguminosae. Nigel C. Veitch
, Nat. Prod. Rep.
, 2007
, 24
, 417
- Synthesis of sophorol, violanone, lonchocarpan, claussequinone, philenopteran, leiocalycin, and some other natural isoflavonoids by the oxidative rearrangement of chalcones with thallium(III) nitrate. Lorànd Farkas, Àgnes Gottsegen, Mihàly Nóagrádi, Sàndor Antus
, J. Chem. Soc., Perkin Trans. 1
, 1974
, 305
- Isoflavonoids of the Leguminosae. Nigel C. Veitch
, Nat. Prod. Rep.
, 2009
, 26
, 776
- Oligomeric isoflavonoids. Part 4.† Synthesis of the daljanelin class of isoflavonoid–neoflavonoid dimers. Mark B. Rohwer, Pieter S. van Heerden, E. Vincent Brandt, Barend C. B. Bezuidenhoudt, Daneel Ferreira
, J. Chem. Soc., Perkin Trans. 1
, 1999
, 3367
- Oligomeric isoflavonoids. Part 1. Structure and synthesis of the first (2,3′)-isoflavone-isoflavan dimer. Barend C. B. Bezuidenhoudt, E. Vincent Brandt, Jacobus A. Steenkamp, David G. Roux, Daneel Ferreira
, J. Chem. Soc., Perkin Trans. 1
, 1988
, 1227
- Synthesis of isoflavanoid oligomers using a pterocarpan as inceptive electrophile. Barend C. B. Bezuidenhoudt, Edward V. Brandt, David G. Roux
, J. Chem. Soc., Perkin Trans. 1
, 1984
, 2767
- The absolute configurations of the animal metabolite, equol, three naturally occurring isoflavans, and one natural isoflavanquinone. K. Kurosawa, W. D. Ollis, B. T. Redman, I. O. Sutherland, O. R. Gottlieb, H. Magalhães Alves
, Chem. Commun. (London)
, 1968
, 1265
- Prenylated isoflavonoids from plants as selective estrogen receptor modulators (phytoSERMs). Rudy Simons, Harry Gruppen, Toine F. H. Bovee, Marian A. Verbruggen, Jean-Paul Vincken
, Food Funct.
, 2012
, 3
, 810
- Asymmetric hydrogenation and transfer hydrogenation in the enantioselective synthesis of flavonoids. Guilherme S. Caleffi, Felipe C. Demidoff, Carmen Nájera, Paulo R. R. Costa
, Org. Chem. Front.
, 2022
, 9
, 1165