Suvi T. M. Simila Martin Group, University of Texas at Austin Group Meeting, Research

1. Utilization of Ring Closing Metathesis in Alkaloid SynthesisI. Synthetic Studies on the Immunosuppressant FR901483 II. Toward the Total Synthesis of Lundurines A-C Suvi T. M. Simila Martin Group, University of Texas at Austin Group Meeting, Research September 17, 2007

2. Utilization of Ring Closing Metathesis in Alkaloid SynthesisI. Synthetic Studies on the Immunosuppressant FR901483 II. Toward the Total Synthesis of Lundurines A-C Suvi T. M. Simila Martin Group, University of Texas at Austin Group Meeting, Research September 17, 2007

3. Retrosynthetic Analysis

4. Addition of the Allylzinc to the ChiralImine Simila, S. T. M.; Martin, S. F. J. Org. Chem.2007, 72, 5342. Model studies: Simila, S. T. M.; Reichelt, A.; Martin, S. F. Tetrahedron Lett.2006, 47, 2933.

5. Weinreb’s ResultsOvershadowing Our Endgame Weinreb. et al. J. Org. Chem.2006, 71, 2046.

6. SummaryPart I • A new route to azaspirane core structure of FR901483 was developed via a • nucleophilic addition to an acyliminium ion followed by a ring-closing metathesis • Lactone-lactam rearrangement gave the azatricyclic core structure of FR901483 • 1-Ethylallylcarbamate protecting group and its cleavage was developed • Allylzinc reagent was developed and it was successfully added to the chiral • imine, however with lack of diastereoselectivitythat persuaded us to divert • our initial studies toward (-)-FR901483

7. II. Toward the Total Synthesis of Lundurines A-CIsolation and Biological Activity • Isolated in 1995 from the leaf extract of the Borneo species Kopsiatenuis • Biological studies were reported in 2004 • Lundurine B is cytotoxic against B16 melanoma cells • (in vitro); 2.8 µg/mL • - Unique hexacyclic core containing dihydroindole-cyclopropane moiety • - No reported total syntheses to date Kam, T. S.; Yoganathan, K.; Chuah, C. H. Tetrahedron Lett.1995, 36, 759. Kam, T. S.; Lim, K.; Yoganathan, K.; Hayashi, M.; Komiyama, K. Tetrahedron2004, 60, 10739.

8. Retrosynthetic Analysis

9. Retrosynthetic Analysis

10. Synthesis of the Ugi Components:2-Vinyltryptamine Trivinylboroxane: O’Shea, et. al. J. Org. Chem.2002, 67, 4968.

11. Synthesis of the Ugi Components:Masked Divinylketone Blicke, F.; McCarty, F. et. al. J. Org. Chem. 1959, 24, 1376. Sapi, J. et. al. Synthesis1988, 619. Ward, D. E. et. al. J. Org. Chem. 2002, 67, 1618. Detty, M. L. et. al. Organometallics1992, 11, 2157. Angiolini, L. et al. Polymer1989, 30, 564.

12. Successful Ugi Reactions Hoffmann type elimination trials of the methyl piperidine ring unsuccessful Convertible isocyanide: Armstrong, R. W.; Keating, T. A. J. Am. Chem. Soc.1999, 118, 2574.

13. Ugi with the Thiopyranone Sulfoxide eliminations: Rapoport, H. et. al. J. Org. Chem.1980, 45, 4817. Galons, H. et. al. Synth. Commun, 1991, 21, 1743.

14. Ugi with Bisthiophenylpentanone

15. Ugi with the 5-Methoxy-2-vinyltryptamine

16. Protected Tryptamine Piece

17. Ugi with the 5-Methoxy-2-vinyltryptamine

18. Synthesis of the RCM Precursor

19. Execution of the Back-up Plan

20. Preparation of the Divinylglycine Piece Bis-conjugate addition: Galons, H. et. al. Synth. Commun, 1991, 21, 1743.

21. Preparation of the Divinylglycine Piece Bis-conjugate addition: Galons, H. et. al. Synth. Commun, 1991, 21, 1743.

22. Successful Formation of the RCM Precursors

23. Tandem-RCM Attempts Grubbs catalysts: Grubbs, R. H. Angew. Chem. Int. Ed, 2006, 45, 3760. Lance: Grubbs, R. H. et. al. Org. Lett. 2007, 9, 1589. Schrock catalysts: Schrock, R. R. Angew. Chem. Int. Ed. 2006, 45, 3748.

24. Possible Explanations for Unsuccessful RCM Modes of catalyst inhibition: Grubbs, R. H. Acc. Chem. Res, 1995, 28, 446.

25. Troubleshooting the Functional Group Problems

26. Troubleshooting the Functional Group Problems Examples of 8-membered RCM: Martin, S. F. et. al. Tetrahedron Lett.1994, 35, 691. Lubell, W. D. et. al. J. Org. Chem.2005, 70, 3838. Rodriguez, J. Angew. Chem. Int. Ed.2006, 45, 5740. Bennasar, M.-L. Tetrahedron, 2007, 63, 861.

27. Ts-indole and Cyanide in Place of the t-Butyl Ester //

28. Methyl Ester in Place of the t-Butyl Ester

29. Methyl Ester in Place of the t-Butyl Ester

30. Reduction of the Ester

31. Substrate for 8-Membered Ring Closure

32. End Game

33. SummaryPart II • Ugi reactions with cyclic ketones appeared to give better results than acyclic • Successful route to the RCM precursor via Ugi was developed; however, the • low yielding Ugi step steered us to develop another route • Bisalkylation of an imine, reductive amination and acylation/alkylation provided • an efficient route to the RCM precursors • Preliminary experiments to cyclize 5- and 8-membered rings have been • accomplished and further studies are in progress

34. Acknowledgements University of Texas at Austin Prof. Stephen F. Martin Martin Group Lab 1 $$$$$$ Robert A. Welch Foundation NIH (GM 25439) Roche Pfizer Merck Materia Inc. for catalyst support Prof. Robert H. Grubbs for catalyst support

36. Woerpel: Inside Addition Woerpel K. A. et al. J. Am. Chem. Soc.1999, 121, 12208.

37. Addition to the Acyl Iminium IonWoerpel’s Model Stereoselective additions to oxonium ions: Woerpel, K. A. et al. J. Am. Chem. Soc.1999, 121, 12208. Stereoselective additions to iminium ions: Martin, S. F.; Bur, S. K. Org. Lett. 2000, 2, 3445; Tetrahedron Lett. 1997, 38, 7641.

38. Hydroboration of the Azaspirane Predicted selectivity:

39. Development of a New Protecting GroupSubstituted Alloc

40. Development of the Deprotection Conditions *) 10-mol% Pd(PPh3)4

41. Allylsilane Addition Allylsilane acid synthesis: Weiler, L. Can. J. Chem.1983, 61, 2530.

42. Staudinger/Aza-Wittig/Ugi

43. Towards the Divinyl Functionality