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
作者:Satoshi YAMAUCHI、Yoshihiro KINOSHITA、Yoshiro KINOSHITA
DOI:10.1271/bbb.67.1959
日期:2003.1
(R) and (S)-Aldehydes 2, which are intermediates for the synthesis of (5R) and (5S)-HETE, were respectively synthesized from the yeast-mediated reductive products, hydroxy ester 3 and cis-lactone 4, through Baeyer-Villiger oxidation with complete retention of enantiomeric excess.
(R)和(S)-醛2是合成(5R)和(5S)-HETE的中间体,分别通过酵母介导的还原产物羟基酯3和顺式内酯4通过Baeyer合成-维利格氧化,完全保留对映体过量。