1 / 31

Lewis Acid and Br Ø nst Acid Catalyzed Diazo Compounds Rearrangement

Lewis Acid and Br Ø nst Acid Catalyzed Diazo Compounds Rearrangement. 吴佩煜 2013.4.13. Contents. Introduction 1,2-H shift 1,2-aryl shift Intramolecular nucleophilic attack Ring expansion reaction Conclusion. Introduction. Introduction. Ring expansion reaction. 1,2-H shift. 1,2-H shift.

verena
Télécharger la présentation

Lewis Acid and Br Ø nst Acid Catalyzed Diazo Compounds Rearrangement

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Lewis Acid and BrØnst Acid Catalyzed Diazo Compounds Rearrangement 吴佩煜 2013.4.13

  2. Contents • Introduction • 1,2-H shift • 1,2-aryl shift • Intramolecularnucleophilic attack • Ring expansion reaction • Conclusion

  3. Introduction

  4. Introduction Ring expansion reaction

  5. 1,2-H shift

  6. 1,2-H shift Roskamp, E. J. J. Org. Chem. 1989,54, 3258-3260 Feng, X. J. Am. Chem. Soc. 2010, 132, 8532–8533

  7. 1,2-H shift Maruoka, K. J. Am. Chem. Soc. 2009, 131, 11280–11281

  8. 1,2-H shift Hwang, G. and Ryu, D. H. Angew. Chem. Int. Ed. 2012, 51, 8322 –8325

  9. 1,2-H shift Kingsbury, J. S. Org. Lett., 2009, 11, 3202-3205

  10. 1,2-aryl shift

  11. 1,2-aryl shift Maruoka, K. J. Am. Chem. Soc. 2008, 130, 2434-2435

  12. 1,2-aryl shift Barluenga, J. and Valdés C. Nature Chem. 2009, 1, 494-499

  13. 1,2-aryl shift

  14. 1,2-aryl shift Carreira, E. M. Angew. Chem. Int. Ed. 2011, 50, 9085 –9088

  15. 1,2-aryl shift

  16. Intramolecularnucleophilic attack

  17. Intramolecularnucleophilic attack Maruoka, K. J. Am. Chem. Soc. 2008, 130, 14380-14381

  18. Intramolecularnucleophilic attack Akiyama, T. Org. Lett., 2009, 11, 2445-2447

  19. Intramolecularnucleophilic attack Maruoka, K. Org. Lett., 2010, 12, 1668-1671

  20. Ring expansion reaction Ring expansion reaction

  21. Ring expansion reaction Kingsbury, J. S. J. Am. Chem. Soc. 2009, 131, 878-879

  22. Ring expansion reaction Maruoka, K. J. Am. Chem. Soc. 2009, 131, 6614-6617

  23. Ring expansion reaction Kingsbury, J. S. Org. Lett., 2010, 12, 3598-3601

  24. Ring expansion reaction Maruoka, K. Chem. Commun. 2010, 46, 6810–6812

  25. Ring expansion reaction Kingsbury, J. S. Org. Lett., 2011, 13, 2004-2007

  26. Ring expansion reaction Maruoka, K. J. Am. Chem. Soc. 2011, 133, 8834-8837

  27. Ring expansion reaction Pellicciari, R. J. Org. Chem. 2011,76, 7431-7437

  28. Ring expansion reaction

  29. Ring expansion reaction Feng, X. Angew. Chem. Int. Ed. 2012, 51, 8644 –8647 Feng, X. J. Am. Chem. Soc. 2011, 133, 15268-15271

  30. Conclusion • Chemoselectivity • Regioselectivity • Stereoselective and enantioselectivity

  31. Thanks !

More Related