Literature DB >> 16153414

Circular dichroism, a powerful tool for the assessment of absolute configuration of flavonoids.

Desmond Slade1, Daneel Ferreira, Jannie P J Marais.   

Abstract

Circular dichroism is a powerful tool for establishing the absolute configuration of flavonoids and proanthocyanidin analogues. It has been utilized to study the configuration of flavanones, dihydroflavonols (3-hydroxyflavanones), flavan-3-ols, flavan-4-ols, flavan-3,4-diols, flavans, isoflavans, isoflavanones, pterocarpans, 6a-hydroxypterocarpans, rotenoids, 12a-hydroxyrotenoids, neoflavonoids, 3,4-dihydro-4-arylcoumarins, 4-arylflavan-3-ols, auronols, homoisoflavanones, proanthocyanidins, and various classes of biflavonoids. Results relevant to the correlation of circular dichroic data and the absolute configuration of the diastereoisomers of some of the above classes of compounds will be discussed.

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Year:  2005        PMID: 16153414     DOI: 10.1016/j.phytochem.2005.02.002

Source DB:  PubMed          Journal:  Phytochemistry        ISSN: 0031-9422            Impact factor:   4.072


  61 in total

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10.  Dynamic residual complexity of the isoliquiritigenin-liquiritigenin interconversion during bioassay.

Authors:  Charlotte Simmler; Atieh Hajirahimkhan; David C Lankin; Judy L Bolton; Tristesse Jones; Djaja D Soejarto; Shao-Nong Chen; Guido F Pauli
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