![Page 1: Total Synthesis of Jerangolid D - University of Pittsburghccc.chem.pitt.edu/wipf/Current Literature/nilu_9.pdf2007/03/18 · Total Synthesis of Jerangolid D Jiri Pospisil and Istvan](https://reader031.vdocuments.us/reader031/viewer/2022012003/60a5788c386a14126f7b5838/html5/thumbnails/1.jpg)
Total Synthesis of Jerangolid D
Jiri Pospisil and Istvan E. MarkoCatholic University of Louvain, Belgium
JACS ASAP
Nilu Jayasuriya @ Wipf Group 1 3/18/2007
![Page 2: Total Synthesis of Jerangolid D - University of Pittsburghccc.chem.pitt.edu/wipf/Current Literature/nilu_9.pdf2007/03/18 · Total Synthesis of Jerangolid D Jiri Pospisil and Istvan](https://reader031.vdocuments.us/reader031/viewer/2022012003/60a5788c386a14126f7b5838/html5/thumbnails/2.jpg)
Jerangolid• Isolated from
myxobacteriumSorangium cellulosum
• Anti-fungal agentsactivity againstHansenula anolmala andMucor hiemalis (70ng/mL); Pichiamembranaefaciens,Debaryomyces hansenii,Trichosoron terrestre(0.1-0.4 µg/mL), andTrichoderma hamata,Botritis cinerea, andCandida albicans (4-7 µg/mL)
• Mechanism of actionunknown
Gerth, K.; Washausen, P.; Hofle, G.; Irschik, H.; Reichenbach, H. J. Antibiot. 1996, 49, 71-75.
Nilu Jayasuriya @ Wipf Group 2 3/18/2007
![Page 3: Total Synthesis of Jerangolid D - University of Pittsburghccc.chem.pitt.edu/wipf/Current Literature/nilu_9.pdf2007/03/18 · Total Synthesis of Jerangolid D Jiri Pospisil and Istvan](https://reader031.vdocuments.us/reader031/viewer/2022012003/60a5788c386a14126f7b5838/html5/thumbnails/3.jpg)
Myxobacteria• Unicellular rod-shaped bacteria• Found in soil• Move by gliding• Synthesize a large number of
biologically active secondarymetabolites
Dawid, W.; FEMS Microbiology Rev. 2000, 24, 403-427.
Nilu Jayasuriya @ Wipf Group 3 3/18/2007
![Page 4: Total Synthesis of Jerangolid D - University of Pittsburghccc.chem.pitt.edu/wipf/Current Literature/nilu_9.pdf2007/03/18 · Total Synthesis of Jerangolid D Jiri Pospisil and Istvan](https://reader031.vdocuments.us/reader031/viewer/2022012003/60a5788c386a14126f7b5838/html5/thumbnails/4.jpg)
Ambruticin/Jerangolid
• Activity of Ambruticin andJerangolid are similar
• Mode of action- affects theosmoregulation system ofsusceptible fungi
• Increase the amount of glyceroland accumulation of fatty acids,cells starts leaking results in celldeath.
Genet, J-P.; Michelet, V. Curr. Org. Chem. 2005, 9, 405-418.
Nilu Jayasuriya @ Wipf Group 4 3/18/2007
![Page 5: Total Synthesis of Jerangolid D - University of Pittsburghccc.chem.pitt.edu/wipf/Current Literature/nilu_9.pdf2007/03/18 · Total Synthesis of Jerangolid D Jiri Pospisil and Istvan](https://reader031.vdocuments.us/reader031/viewer/2022012003/60a5788c386a14126f7b5838/html5/thumbnails/5.jpg)
Previous synthesis of Abruticin-eastern fragment
Kende, 1990: Hetero-Diels Alder/Ireland-ClaisenJacobsen 2001:
Martin, 2001:
Kende et al. J. Am. Chem. Soc. 1990, 112, 9645.;Jacobsen, E.; Liu, P. J. Am. Chem. Soc. 2001, 123, 10772;Martin, S et al. Tetrahedron 2003, 59, 6819.; Lee et al. Angew. Chem. Int. Ed. 2002, 41, 176.
Lee, 2002: Auxiliary/Metathesis
Nilu Jayasuriya @ Wipf Group 5 3/18/2007
![Page 6: Total Synthesis of Jerangolid D - University of Pittsburghccc.chem.pitt.edu/wipf/Current Literature/nilu_9.pdf2007/03/18 · Total Synthesis of Jerangolid D Jiri Pospisil and Istvan](https://reader031.vdocuments.us/reader031/viewer/2022012003/60a5788c386a14126f7b5838/html5/thumbnails/6.jpg)
Nilu Jayasuriya @ Wipf Group 6 3/18/2007
![Page 7: Total Synthesis of Jerangolid D - University of Pittsburghccc.chem.pitt.edu/wipf/Current Literature/nilu_9.pdf2007/03/18 · Total Synthesis of Jerangolid D Jiri Pospisil and Istvan](https://reader031.vdocuments.us/reader031/viewer/2022012003/60a5788c386a14126f7b5838/html5/thumbnails/7.jpg)
Nilu Jayasuriya @ Wipf Group 7 3/18/2007
![Page 8: Total Synthesis of Jerangolid D - University of Pittsburghccc.chem.pitt.edu/wipf/Current Literature/nilu_9.pdf2007/03/18 · Total Synthesis of Jerangolid D Jiri Pospisil and Istvan](https://reader031.vdocuments.us/reader031/viewer/2022012003/60a5788c386a14126f7b5838/html5/thumbnails/8.jpg)
Nilu Jayasuriya @ Wipf Group 8 3/18/2007
![Page 9: Total Synthesis of Jerangolid D - University of Pittsburghccc.chem.pitt.edu/wipf/Current Literature/nilu_9.pdf2007/03/18 · Total Synthesis of Jerangolid D Jiri Pospisil and Istvan](https://reader031.vdocuments.us/reader031/viewer/2022012003/60a5788c386a14126f7b5838/html5/thumbnails/9.jpg)
Nilu Jayasuriya @ Wipf Group 9 3/18/2007
![Page 10: Total Synthesis of Jerangolid D - University of Pittsburghccc.chem.pitt.edu/wipf/Current Literature/nilu_9.pdf2007/03/18 · Total Synthesis of Jerangolid D Jiri Pospisil and Istvan](https://reader031.vdocuments.us/reader031/viewer/2022012003/60a5788c386a14126f7b5838/html5/thumbnails/10.jpg)
Silyl modified Sakurai
Marko, I.; Mekhalfia, A. Tetrahedron Lett. 1991, 32(36), 4779-4782.Marko, I.; Mekhalfia, A.; Adams, H. Tetrahedron Lett. 1991, 32(36), 4779-4782.
-1990
-1991: Intramolecular
Nilu Jayasuriya @ Wipf Group 10 3/18/2007
![Page 11: Total Synthesis of Jerangolid D - University of Pittsburghccc.chem.pitt.edu/wipf/Current Literature/nilu_9.pdf2007/03/18 · Total Synthesis of Jerangolid D Jiri Pospisil and Istvan](https://reader031.vdocuments.us/reader031/viewer/2022012003/60a5788c386a14126f7b5838/html5/thumbnails/11.jpg)
Sakurai AMCR
Nilu Jayasuriya @ Wipf Group 11 3/18/2007
![Page 12: Total Synthesis of Jerangolid D - University of Pittsburghccc.chem.pitt.edu/wipf/Current Literature/nilu_9.pdf2007/03/18 · Total Synthesis of Jerangolid D Jiri Pospisil and Istvan](https://reader031.vdocuments.us/reader031/viewer/2022012003/60a5788c386a14126f7b5838/html5/thumbnails/12.jpg)
Nilu Jayasuriya @ Wipf Group 12 3/18/2007
![Page 13: Total Synthesis of Jerangolid D - University of Pittsburghccc.chem.pitt.edu/wipf/Current Literature/nilu_9.pdf2007/03/18 · Total Synthesis of Jerangolid D Jiri Pospisil and Istvan](https://reader031.vdocuments.us/reader031/viewer/2022012003/60a5788c386a14126f7b5838/html5/thumbnails/13.jpg)
Nilu Jayasuriya @ Wipf Group 13 3/18/2007
![Page 14: Total Synthesis of Jerangolid D - University of Pittsburghccc.chem.pitt.edu/wipf/Current Literature/nilu_9.pdf2007/03/18 · Total Synthesis of Jerangolid D Jiri Pospisil and Istvan](https://reader031.vdocuments.us/reader031/viewer/2022012003/60a5788c386a14126f7b5838/html5/thumbnails/14.jpg)
Summary
• First total synthesis of Jerangolid in 22 steps in 6.1% overall yield.
• Utilized the silyl modified sakurai reaction
• Synthesis of analogues and other members of the Jerangolid family
Nilu Jayasuriya @ Wipf Group 14 3/18/2007