Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000131.xml
Synfacts 2010(7): 0738-0738
DOI: 10.1055/s-0029-1220107
DOI: 10.1055/s-0029-1220107
Synthesis of Natural Products and Potential Drugs
© Georg Thieme Verlag
Stuttgart ˙ New York
Synthesis of Auripyrones A and B
I. Hayakawa, T. Takemura, E. Fukasawa, Y. Ebihara, N. Sato, T. Nakamura, K. Suenaga, H. Kigoshi*
University of Tsukuba and Keio University, Yokohama, Japan
Further Information
Publication History
Publication Date:
22 June 2010 (online)

Significance
Auripyrones A and B were isolated from a sea hare and exhibit cytotoxicity against HeLaS3 cells with the δ-pyrone functional group thought to be important for activity. Auripyrone A has been previously synthesized using a spiroacetalization approach (Angew. Chem. Int. Ed. 2006, 45, 2560), but the absolute configuration of auripyrone B was unknown.