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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
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pubmed:dateCreated |
1995-3-20
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pubmed:abstractText |
The fungus Helminthosporium species NRRL 4671 has been used for the biotransformation of a series of phenyl alkyl sulfides with alkyl groups ranging from methyl to n-hexyl, and benzyl alkyl sulfides with alkyl groups from methyl to n-nonyl. Several 2-phenylethyl and 3-phenylpropyl sulfides have also been examined as substrates, together with cyclohexyl methyl sulfide and 1- and 2-naphthyl methyl sulfides. For the majority of substrates, sulfoxide formation occurred in moderate yield and with predominant (S) chirality at sulfur; lesser amounts of sulfone product were also obtained in some cases. The data so obtained have been used to define the preparatively useful limits of S-oxidation of phenyl alkyl sulfides and benzyl alkyl sulfides by biotransformation using Helminthosporium.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0968-0896
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
2
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
647-52
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:7858971-Biotransformation,
pubmed-meshheading:7858971-Helminthosporium,
pubmed-meshheading:7858971-Isomerism,
pubmed-meshheading:7858971-Magnetic Resonance Spectroscopy,
pubmed-meshheading:7858971-Molecular Structure,
pubmed-meshheading:7858971-Optical Rotation,
pubmed-meshheading:7858971-Oxidation-Reduction,
pubmed-meshheading:7858971-Structure-Activity Relationship,
pubmed-meshheading:7858971-Sulfides,
pubmed-meshheading:7858971-Sulfoxides
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pubmed:year |
1994
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pubmed:articleTitle |
Biotransformation of organic sulfides--IV. Formation of chiral benzyl alkyl and phenyl alkyl sulfoxides by Helminthosporium species NRRL 4671.
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pubmed:affiliation |
Department of Chemistry, Brock University, St. Catharines, Ontario, Canada.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
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