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Q36836490-803FAD40-4F16-4DE2-939A-636C09AEAB13
Q36836490-803FAD40-4F16-4DE2-939A-636C09AEAB13
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http://www.wikidata.org/entity/statement/Q36836490-803FAD40-4F16-4DE2-939A-636C09AEAB13
Complete microbial degradation of both enantiomers of the chiral herbicide mecoprop [(RS)-2-(4-chloro-2-methylphenoxy)propionic acid] in an enantioselective manner by Sphingomonas herbicidovorans sp. nov.
P2860
Q36836490-803FAD40-4F16-4DE2-939A-636C09AEAB13
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36836490-803FAD40-4F16-4DE2-939A-636C09AEAB13
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type
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wasDerivedFrom
2564bdc494f3770132ac52a2b51f4d172a60620d
P2860
Relevance of enantiomeric separations in environmental science.