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STEREODIRECTING SUBSTITUENT EFFECTS DURING ENZYME-CATALYZED SYNTHESIS OF CIS-DIHYDRODIOL METABOLITES OF 1,4-DISUBSTITUTED BENZENE SUBSTRATES
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UNSPECIFIED (1993) STEREODIRECTING SUBSTITUENT EFFECTS DURING ENZYME-CATALYZED SYNTHESIS OF CIS-DIHYDRODIOL METABOLITES OF 1,4-DISUBSTITUTED BENZENE SUBSTRATES. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS (11). pp. 974-976. ISSN 0022-4936.
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Abstract
The cis-dihydrodiol enantiomer preferentially formed, by dioxygenase-catalysed oxidation of 1,4-disubstituted benzene substrates in growing cultures of Pseudomonas putida UV4, is found to be largely controlled by the relative size of the substituents.
Item Type: | Journal Article | ||||
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Subjects: | Q Science > QD Chemistry | ||||
Journal or Publication Title: | JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS | ||||
Publisher: | ROYAL SOC CHEMISTRY | ||||
ISSN: | 0022-4936 | ||||
Official Date: | 7 June 1993 | ||||
Dates: |
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Number: | 11 | ||||
Number of Pages: | 3 | ||||
Page Range: | pp. 974-976 | ||||
Publication Status: | Published |
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