Total syntheses of the immunosuppressants SNF4435 C and D as well as the antibiotics spectinabilin and N-acetyl aureothamine are proposed. These highly unsaturated polypropionates were isolated from various strains of Streptomyces sp. Furthermore, synthetic approaches towards the molluscan polypropionates photodeoxytridachione and crispatene as well as the fungal immunosuppressants candelalide A and B are presented. All natural products feature a terminal gamma-pyrone moiety as a common structural motif. Polyenes consisting of an array of conjugated trisubstituted double bonds have been used as synthetic precursors of the complex polypropionates. The stereoselective assembly of these structures will be further investigated. Preliminary studies have shown that the core bicyclo[4.2.0]octadiene core of SNF4435 compounds can be formed using a highly stereoselective tandem Stille cross-coupling / electrocyclization cascade. A novel Lewis-acid catalyzed cyclization leading to the bicyclo[3.1.0]hexane core of photodeoxytridachione and crispatene has also been developed. The proposed total syntheses provide an opportunity to investigate asymmetric electrocyclization reactions. As opposed to cycloadditions and sigmatropic rearrangements, this class of pericyclic reactions has not yet succumbed to asymmetric catalysis. In a further contribution to synthetic methodology, new approaches towards gamma-pyrones are proposed. The significance of the gamma-pyrone moiety for the biological activity of the natural products will be explored. The biological mode of action of SNF4435C and D remains presently unknown. The natural products do not suppress IL-2 production, distinguishing them from FK506 or cyclosporin A. Our synthetic material and derivatives thereof will be used to isolate binding proteins and gain further insight into of the mechanism of these promising new lead compounds for drug development.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM067636-04
Application #
7064295
Study Section
Medicinal Chemistry Study Section (MCHA)
Program Officer
Schwab, John M
Project Start
2003-05-02
Project End
2008-04-30
Budget Start
2006-05-01
Budget End
2007-04-30
Support Year
4
Fiscal Year
2006
Total Cost
$255,840
Indirect Cost
Name
University of California Berkeley
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
124726725
City
Berkeley
State
CA
Country
United States
Zip Code
94704
Sofiyev, Vladimir; Navarro, Gabriel; Trauner, Dirk (2008) Biomimetic synthesis of the shimalactones. Org Lett 10:149-52
Roethle, Paul A; Chen, Ingrid T; Trauner, Dirk (2007) Total synthesis of (-)-archazolid B. J Am Chem Soc 129:8960-1
Muller, Markus; Kusebauch, Bjorn; Liang, Guangxin et al. (2006) Photochemical origin of the immunosuppressive SNF4435C/D and formation of orinocin through ""polyene splicing"". Angew Chem Int Ed Engl 45:7835-8
Liang, Guangxin; Seiple, Ian B; Trauner, Dirk (2005) Stereoselective syntheses of the bioactive polypropionates aureothin, N-acetylaureothamine, and aureonitrile. Org Lett 7:2837-9
Beaudry, Christopher M; Trauner, Dirk (2005) Total synthesis of (-)-SNF4435 C and (+)-SNF4435 D. Org Lett 7:4475-7
Zuidema, Daniel R; Miller, Aubry K; Trauner, Dirk et al. (2005) Photosensitized conversion of 9,10-deoxytridachione to photodeoxytridachione. Org Lett 7:4959-62
Beaudry, Christopher M; Malerich, Jeremiah P; Trauner, Dirk (2005) Biosynthetic and biomimetic electrocyclizations. Chem Rev 105:4757-78
Barbarow, Jennifer E; Miller, Aubry K; Trauner, Dirk (2005) Biomimetic synthesis of elysiapyrones A and B. Org Lett 7:2901-3
Liang, Guangxin; Miller, Aubry K; Trauner, Dirk (2005) Stereoselective synthesis of cyercene A and the placidenes. Org Lett 7:819-21
Miller, Aubry K; Trauner, Dirk (2005) Mining the tetraene manifold: total synthesis of complex pyrones from Placobranchus ocellatus. Angew Chem Int Ed Engl 44:4602-6

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