Biotransformation of organic sulfides. Part 9. Formation of (S) para-substituted phenyl methyl sulfoxides by biotransformation usingHelminthosporium species NRRL 4671 |
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Authors: | Herbert L. Holland Marc J. Bornmann Gingipalli Lakshmaiah |
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Affiliation: | Department of Chemistry, Brock University, St. Catharines, Ontario, L2S 3A1, Canada |
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Abstract: | Phenyl methyl sulfides substituted in thepara position with methyl, fluoro, chloro, bromo, cyano, nitro, amino, acyl, methoxy, thiomethyl and methylsulfinyl groups have been converted to (S) sulfoxides by biotransformation usingHelminthosporium species NRRL 4671. The highest yields and enantiomeric excesses were obtained with bromo, cyano, methoxy, thiomethyl and methylsulfinyl substituents and in two cases (para-Br and -CN) the products could be crystallized to give (S) sulfoxide of ≥ 96% ee. |
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Keywords: | Biotransformation Enantiotopic selectivity Helminthosporium NRRL 4671 Sulphide Sulphoxidation |
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