Yamauchi, Satoshi <br/><br/>
New method for synthesizing the intermediates to 5-HETE from yeast-mediated reduction products by employing Baeyer-Villiger oxidation with complete retention of enantiomeric excess.  [electronic resource] 

 -  Bioscience, biotechnology, and biochemistry  Sep 2003 
 - 1959-69 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0916-8451 
<br/><br/><label>Standard No.: </label>10.1271/bbb.67.1959  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aldehydes--chemistry<br/>Biotransformation<br/>Cyclopentanes--chemistry<br/>Esters--chemistry<br/>Glycols--chemistry<br/>Hydroxyeicosatetraenoic Acids--biosynthesis<br/>Hydroxylation<br/>Ketones--chemistry<br/>Lactones--chemistry<br/>Oxidation-Reduction<br/>Stereoisomerism<br/>Yeasts--metabolism