1,3-Dipolar cycloadditions in aqueous media

Heterocycles

Volumn 68, Issue 10, 2006, Pages 2177-2202

  Molteni, Giorgio ^a  

^a UNIVERSITY OF MILAN   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 33846498559     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/REV-06-608     Document Type: Article

References (61)

1. Lubineau A., Augé J., and Queneau Y. Synthesis (1994) 741
2. Li C.-J. Chem. Rev. 93 (1993) 2023
3. Li C.-J. Chem. Rev. 105 (2005) 3095
4. Ribe S., and Wipf P. Chem. Commun. (2001) 299
5. In: Grieco P.A. (Ed). Organic Synthesis in Water (1998), Blackie Academic and Professional, London
6. Breslow R. In: Anastas P.T., and Williamson T.C. (Eds). Green Chemistry: Frontiers in Benign Chemical Syntheses and Processes (1998), Oxford University Press, New York Ch. 13
7. Lindström U.M. Chem. Rev. 102 (2002) 2751
8. Kobayashi S., and Manabe K. Acc. Chem. Res. 35 (2002) 209
9. Manabe K., and Kobayashi S. Chem. Eur. J. 8 (2002) 4095
10. Rideout D.C., and Breslow R. J. Am. Chem. Soc. 102 (1980) 7816
11. For a review:. Fringuelli F., Piermatti O., Pizzo F., and Vaccaro L. Eur. J. Org. Chem. (2001) 439
12. Grundmann C., and Richter R. J. Org. Chem. 32 (1967) 2308
13. Bala K., and Hailes H.C. Synthesis (2005) 3423
14. Lubineau A., Bouchain G., and Queneau Y. J. Chem. Soc., Perkin Trans. 1 (1995) 2433
15. Wijnen J.W., Steiner R.A., and Engberts J.B.F.N. Tetrahedron Lett. 36 (1995) 5389
16. Clovis J.S., Eckell A., Huisgen R., and Sustmann R. Chem. Ber. 100 (1967) 60
17. Huisgen R., Seidel M., Wallbillich G., and Knupfer H. Tetrahedron 17 (1962) 3
18. Molteni G., Orlandi M., and Broggini G. J. Chem. Soc., Perkin Trans. 1 (2000) 3742
19. Molteni G., Ponti A., and Orlandi M. New. J. Chem. (2002) 1340
20. Lazaridis T. Acc. Chem. Res. 34 (2001) 931
21. Breslow R. Acc. Chem. Res. 24 (1991) 159
22. Houk K.N., Sims J., Duke R.E., Strozier R.W., and George J.K. J. Am. Chem. Soc. 95 (1973) 7287
23. Houk K.N., Sims J., Watts C.R., and Luskus L.J. J. Am. Chem. Soc. 95 (1973) 7301
24. Houk K.N., and Caramella P. J. Am. Chem. Soc. 98 (1976) 6397
25. Molteni G., and Ponti A. New. J. Chem. (2002) 1346
26. Ch. 3. Caramella P., and Grünanger P. In: Padwa A. (Ed). 1,3-Dipolar Cycloaddition Chemistry Vol. 1 (1984), Wiley-Interscience, New York
27. Huisgen R., Seidel M., Sauer J., McFarland J.W., and Wallbillich G. J. Org. Chem. 24 (1959) 892
28. Huisgen R., Grashey R., Seidel M., Wallbillich G., Knupfer H., and Schmidt R. Ann. Chem. 653 (1962) 105
29. Molteni G., and Del Buttero P. Heterocycles 65 (2005) 1183
30. Molteni G. Tetrahedron. Asymmetry 15 (2004) 1077
31. (S). Rajaeian E., Monajjemi M., and Gholami M.R. J. Chem. Res. (2003) 91
32. Inoue Y., Araki K., and Shiraishi S. Bull. Chem. Soc. Jpn. 64 (1991) 3079
33. van Mersbergen D., Wijnen J.W., and Engberts J.B.F.N. J. Org. Chem. 63 (1998) 8801
34. Sauer J., and Sustmann R. Angew. Chem., Int. Ed. Engl. 19 (1980) 779
35. Huisgen R. Pure Appl. Chem. 52 (1980) 2283
36. Curran D.P., Kim B.H., Piyasena H.P., Loncharic R.J., and Houk K.N. J. Org. Chem. 52 (1987) 2137
37. Rispens T., and Engberts J.B.F.N. J. Phys. Org. Chem. 18 (2005) 908
38. Rispens T., and Engberts J.B.F.N. J. Phys. Org. Chem. 18 (2005) 725
39. Dignam K.J., Hegarty A.F., and Quain P.L. J. Org. Chem. 43 (1978) 388
40. Lee G.A. Synthesis (1982) 508
41. Earhart R.H., and Neil G.L. Adv. Enzyme Regulation 24 (1985) 179
42. Rolhoff J.C., Robinson III J., and Gardner J.O. Tetrahedron Lett. 33 (1992) 3113
43. (S). Adembri G., Poli M.L., and Sega A. J. Chem. Res. 126 (2003)
44. Bast K., Christl M., Huisgen R., Mack W., and Sustmann R. Chem. Ber. 106 (1973) 3258
45. Rama Rao K., Bhanumathi N., Snirivasan T.N., and Sattur P.B. Tetrahedron Lett. 31 (1990) 899
46. Rama Rao K., Bhanumathi N., and Sattur P.B. Tetrahedron Lett. 31 (1990) 3201
47. Easton C.J., Huges C.M.M., Tiekink E.R.T., Savage G.P., and Simpson G.W. Tetrahedron Lett. 36 (1995) 629
48. Meyer A.G., Easton C.J., Lincoln S.F., and Simpson G.W. Chem. Commun. (1997) 1517
49. Meyer A.G., Easton C.J., Lincoln S.F., and Simpson G.W. J. Org. Chem. 63 (1998) 9069
50. Matsui Y., Nishioka T., and Fujita T. Top. Curr. Chem. 128 (1985) 61
51. Chu J.-H., Li W.-S., Chao I., Lee G.-H., and Chung W.-S. Tetrahedron 62 (2006) 7380
52. Fusco R., Garanti L., and Zecchi G. Chim. Ind (Milan) 57 (1975) 16
53. Bala K., and Hailes H.C. Synthesis (2005) 3423
54. Zerressen A., and Jäschke A. J. Mol. Evol. 61 (2005) 236
55. Mineno T., and Miller M.J. J. Org. Chem. 68 (2003) 6591
56. Parliament M.B., Chapman J.D., Urtasun R.C., McEwan A.J., Golberg L., Mercer J.R., Mannan R.H., and Wiebe L.I. Br. J. Cancer 65 (1992) 90
57. Scobie M., and Threadgill M.D. J. Org. Chem. 59 (1994) 7008
58. Jiang N., and Li C.-J. Chem. Commun. (2004) 394
59. Kolb H.C., Finn M.G., and Sharpless K.B. Angew. Chem. Int. Ed. Engl. 40 (2001) 2004
60. Block V.D., Hiemstra H., and van Maarseveen J.H. Eur. J. Org. Chem. (2006) 51
61. Huisgen R., Grashey R., Seifeld M., Wallbillich G., Knupfer H., and Schmidt R. Ann. Chem. 653 (1962) 105