Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
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Rhodium(II)-Catalyzed Reaction of Iodonium Ylides with Heterocyclic and Aromatic Compounds. Effecient Synthesis of Fused Acetals and C-H Insertion Products

  • Published : 2002.05.20
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References

  1. Koser, G. F. In The Chemistry of Functional Groups, SupplementD; Wiley: New York, 1983.
  2. Varvoglis, A. In The Organic Chemistryof Polycoordinated Iodine, VCH Publishers: New York, 1992.
  3. Varvoglis, A. In Hypervalent Iodine in Organic Synthesis, AcademicPress: London, 1997.
  4. Moriarty, R. M.; Kim, J.; Guo, L. Tetrahedron Lett. 1993, 34,4129. https://doi.org/10.1016/S0040-4039(00)60509-9
  5. Hadjiarapoglou, L. P.; Spyroudis, S.; Varvoglis, A. J. Am.Chem. Soc. 1985, 107, 7178. https://doi.org/10.1021/ja00310a072
  6. Hadjiarapoglou, L. P.; Schank, K.Tetrahedron Lett. 1989, 30, 6673. https://doi.org/10.1016/S0040-4039(00)70647-2
  7. Hadjiarapoglou, L. P.; Varvoglis,A. Synthesis 1988, 913.
  8. Hadjiarapoglou, L. P.; Schank, K.Tetrahedron 1997, 53, 9365. https://doi.org/10.1016/S0040-4020(97)00589-9
  9. Asouti, A.; Hadjiarapoglou, L. P.Tetrahedron Lett. 1998, 39, 9073. https://doi.org/10.1016/S0040-4039(98)01997-2
  10. Kume, M.; Kubota, T.; Iso, Y. Tetrahedron Lett. 1995, 36, 8043. https://doi.org/10.1016/0040-4039(95)01703-K
  11. Spyroudis, S.; Tarantili, P. Tetrahedron 1994, 50, 11541. https://doi.org/10.1016/S0040-4020(01)89291-7
  12. Moriarty, R. M.; May, E. J.; Guo, L.; Prakash, O. TetrahedronLett. 1998, 39, 765. https://doi.org/10.1016/S0040-4039(97)10620-7
  13. Moriarty, R. M.; May, E. J.; Prakash, O. TetrahedronLett. 1997, 38, 4333. https://doi.org/10.1016/S0040-4039(97)00967-2
  14. Moriarty, R. M.; Prakash, O.; Vaid,R. K.; Zhao, L. J. J. Am. Chem. Soc. 1989, 111, 6443. https://doi.org/10.1021/ja00198a078
  15. Papadopoulou, M.; Spyroudis, S.; Varvoglis, A. J. Org. Chem.1985, 50, 1509. https://doi.org/10.1021/jo00209a029
  16. Spyroudis, S.; Tarantili, P. J. Org. Chem. 1993,58, 4885. https://doi.org/10.1021/jo00070a025
  17. Koser, G. F.; Yu, S.-M. J. Org. Chem. 1975, 40, 1166. https://doi.org/10.1021/jo00896a037
  18. Castellino, A. J.; Rapoport, H. J. Org. Chem. 1986, 51, 1006. https://doi.org/10.1021/jo00357a011
  19. McGuire, S. M.; Townsend, C. A. Bioorg. Med. Chem. Lett. 1993, 3,653. https://doi.org/10.1016/S0960-894X(01)81247-6
  20. Wolff, S.; Hoffman, H. M. R. Synthesis 1988, 760.
  21. Bujons, J.;Sanchez-Baeza, F.; Messaguer, A. Tetrahedron Lett. 1992, 33,6387. https://doi.org/10.1016/S0040-4039(00)60980-2
  22. Sullivan, B.; Faulkner, D. J. J. Org. Chem. 1984, 49, 3204. https://doi.org/10.1021/jo00191a030
  23. Bobzin, S. C.; Faulkner, D. J. J. Org. Chem. 1989, 54, 5727. https://doi.org/10.1021/jo00285a019
  24. Merritt, A. T.; Leg, S. V. Nat. Prod. Rep. Lett. 1992, 243.
  25. Nishiyama, S.; Kanai, H.; Yamamura, S. Bull. Chem. Soc. Jpn.1990, 63, 1332.
  26. Tadano, K.; Yamada, H.; Idogaki, Y.; Ogawa, S.;Suami, T. Tetrahedron Lett. 1988, 29, 655. https://doi.org/10.1016/S0040-4039(00)80175-6
  27. Tadano, K.; Yamada,H.; Idogaki, Y.; Ogawa, S.; Suami, T. Tetrahedron 1990, 46, 2353. https://doi.org/10.1016/S0040-4020(01)82015-9
  28. Schreiber, S. L.; Satake, K. J. Am. Chem. Soc. 1984, 106, 4186. https://doi.org/10.1021/ja00327a020
  29. Schreiber, S. L.; Satake, K. Tetrahedron Lett. 1986, 27, 2575. https://doi.org/10.1016/S0040-4039(00)84588-8
  30. deJesus, A. E.; Steyn, P. S.; Vleggaar, R. J. Chem. Soc., Chem. Commun.1985, 1633.
  31. Fernandez, M. C.; Esquivel, B.; Cardenas, J.; Sanchez, A. A.;Toscano, R. A.; Rodriguez-Hahn, L. Tetrahedron 1991, 47, 7199. https://doi.org/10.1016/S0040-4020(01)89722-2
  32. Okuyama, E.; Yamazaki, M. Tetrahedron 1983, 24, 3113.
  33. Pirrung, M. C.; Lee, Y. R. Tetrahedron Lett. 1996, 37, 2391. https://doi.org/10.1016/0040-4039(96)00412-1
  34. Kraus, G. A.; Johnston, B. E.; Applegate, J. M. J. Org. Chem.1991, 56, 5688. https://doi.org/10.1021/jo00019a042
  35. Mellor, J. M.; Mohammed, S. Tetrahedron 1993, 49, 7557. https://doi.org/10.1016/S0040-4020(01)87230-6
  36. Roy, S. C.; Mandal, P. K. Tetrahedron 1996, 52, 12495. https://doi.org/10.1016/0040-4020(96)00728-4
  37. Chen, F.-E.; Fu, H.; Meng, G.; Cheng, Y.; Hu, Y.-L. Synthesis2000, 1091.
  38. Pirrung, M. C.; Zhang, J.; Lackey, K.; Sternbach, D. D.; Brown, F.J. Org. Chem. 1995, 60, 2112. https://doi.org/10.1021/jo00112a036

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