Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1373741 | Bioorganic & Medicinal Chemistry Letters | 2009 | 4 Pages |
Abstract
Hexylitaconic acid (1) is an intriguing natural product possessing a chiral carbon, and both its enantiomers have been found in nature. Enantiomeric pure (+)-(1) and (−)-(1) were successfully prepared by racemic synthesis followed by enantiomeric separation in a chiral HPLC system. Their absolute configurations were clarified by the vibrational circular dichroism technique using their methyl esters 2 and lactones 3. Their inhibitory activities against the interaction of p53–HDM2 were also examined.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Atsufumi Nakahashi, Nobuaki Miura, Kenji Monde, Sachiko Tsukamoto,