Proceedings of the PSK Conference (대한약학회:학술대회논문집)
- 2002.10a
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- Pages.345.3-346
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- 2002
Diastereoselective Synthesis of (+)-Frontalin
- Jung, Jung-Hwa (College of Pharmacy. Sookmyung Women′s University) ;
- Kim, Hee-Doo (College of Pharmacy. Sookmyung Women′s University)
- Published : 2002.10.01
Abstract
In connection with the asymmetric synthesis of chiral l.2-diol. we report here the total synthesis of (+)-frontalin using diastereoselective alkylation featuring tridentate chelation-controlled asymmetric alkylation of a-hydroxyketone, in which the chiral auxiliary is attached to the hydroxyl group as ether linkage. The starting D-glyceraldehyde acetonide was converted (S)- [(4R)-2.2-dimethyH,3-dioxolan-4-yl] (4-methoxyphenyl) methanol. (omitted)
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