2011
DOI: 10.1007/s10311-011-0315-5
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First evidence for a stereoselective incorporation of nonylphenol diastereomers in soil-derived organo-clay complexes

Abstract: Environmental processes can affect the stereochemical properties of organic pollutants. In particular, biotic processes like microbial transformations or membrane penetration alter the ratios of enantiomers as well as diastereomers. These effects have been intensively used not only in environmental studies but also in medicine, toxicology, pharmacy, and agricultural sciences. However, in order to identify unambiguously biotic-initiated alteration of organic compounds, the knowledge on the stereoselective effec… Show more

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Cited by 15 publications
(2 citation statements)
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“…Chirality is a growing area of research in the field of environmental chemistry. The enantiomers of a chiral pesticide have identical physicochemical properties, while diastereoisomers/epimers may differ in their physicochemical properties. , However, in chiral environments such as biological systems, enantiomers of the same diastereomer display selectivity and thus may differ in toxicity . Liu et al conducted a comprehensive investigation of the enantioselective behavior of pyrethroids and organophosphates and consistently observed differences in toxicity on nontarget organisms among enantiomers.…”
Section: Introductionmentioning
confidence: 99%
“…Chirality is a growing area of research in the field of environmental chemistry. The enantiomers of a chiral pesticide have identical physicochemical properties, while diastereoisomers/epimers may differ in their physicochemical properties. , However, in chiral environments such as biological systems, enantiomers of the same diastereomer display selectivity and thus may differ in toxicity . Liu et al conducted a comprehensive investigation of the enantioselective behavior of pyrethroids and organophosphates and consistently observed differences in toxicity on nontarget organisms among enantiomers.…”
Section: Introductionmentioning
confidence: 99%
“…29,47 Na biodegradação, ecotoxicidade e destino ambiental, o reconhecimento de enantiosseletividade é essencial para fornecer uma avaliação de risco mais realista de compostos quirais. [48][49][50][51][52][53][54] 56 constatando-se que a maioria desses estudos é realizada somente com misturas racémicas. Um estudo recente realizado por Connors et al 57 demonstrou que, em modelos animais, o metabolismo enantiosseletivo dos FQ não pode ser diretamente extrapolado a partir dos dados disponíveis para o organismo humano.…”
Section: Fármacos Quiraisunclassified