A one-pot synthesis of substituted salicylnitriles

Tetrahedron Letters

Volumn 49, Issue 28, 2008, Pages 4443-4445

  Anwar, Hany F ^a   Hansen, Trond Vidar ^a  

^a UNIVERSITY OF OSLO   (Norway)

Author keywords

IBX; ortho Formylation; Phenols; Salicylnitriles

Indexed keywords

AMMONIA; IMINE; MAGNESIUM CHLORIDE; NITRILE; PARAFORMALDEHYDE; PHENOL DERIVATIVE; SALICYLALDEHYDE; SALICYLNITRILE DERIVATIVE; TETRAHYDROFURAN; TRIETHYLAMINE;

ARTICLE; CHEMICAL STRUCTURE; ONE POT SYNTHESIS; OXIDATION; SUBSTITUTION REACTION;

EID: 44649140522     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2008.05.006     Document Type: Article

References (41)

1. Pongratz A. Monatsh. Chem. 48 (1927) 585-591
2. Pongratz A., and Pochmuler E. Monatsh. Chem. 51 (1929) 228-233
3. von Braun J., and Manz G. Liebigs Ann. Chem. 488 (1931) 111-126
4. Rosemund K.W., and Struck E. Chem. Ber. 52B (1919) 1749-1756
5. Herr R.J. Bioorg. Med. Chem. 10 (2002) 3379-3393
6. Schmidt A. In: Murahashi S.-I. (Ed). Science of Synthesis Vol. 19 (2004), Georg Thieme 133-161
7. Larock R. Comprehensive Organic Transformations. A Guide to Functional Group Preparations (1989), VCH, New York
8. Lindley J. Tetrahedron 40 (1984) 1433-1456
9. Ellis G.P., and Romney-Alexander T.M. Chem. Rev. 87 (1987) 779-794
10. Sundermeier M., Zapf A., and Beller M. Eur. J. Inorg. Chem. (2003) 3513-3526
11. Cristau H.-J., Ouali A., Spindler J.-F., and Tailefer M. Chem. Eur. J. 11 (2005) 2483-2492 and references cited therein
12. Ellis G.P., and Hudson H.V. J. Chem. Res. (S) (1985) 372-373
13. Jones T.H., Blum M.S., and Fales H.M. Synth. Commun. 11 (1981) 889-894
14. Shah M.V., and Sethna S. J. Chem. Soc. (1961) 2663-2666
15. Bigi F., Maggi R., Sartori G., Casnati G., and Bocelli G. Gazz. Chim. Ital. 122 (1992) 283-289
16. Adachi M., and Sugasawa T. Synth. Commun. 20 (1990) 71-84
17. Hofsløkken N.U., and Skattebøl L. Acta Chem. Scand. 53 (1999) 258-262
18. Hansen T.V., and Skattebøl L. Org. Synth. 82 (2005) 64-68
19. Anwar H.F., Skattebøl L., and Hansen T.V. Tetrahedron 63 (2007) 9997-10002
20. Hansen T.V., and Skattebøl L. Tetrahedron Lett. 46 (2005) 3829-3830
21. Hansen T.V., and Skattebøl L. Tetrahedron Lett. 46 (2005) 3357-3358
22. Odlo K., Klaveness J., Rongved P., and Hansen T.V. Tetrahedron Lett. 47 (2006) 1101-1103
23. Anwar H.F., Skattebøl L., Skramstad J., and Hansen T.V. Tetrahedron Lett. 46 (2005) 5285-5287
24. Varvoglis A. Hypervalent Iodine in Organic Synthesis (1997), Academic Press, London
25. Wirth T., and Hirt U.H. Synthesis (1999) 1271-1287
26. Frigerio M., and Santagostino M. Tetrahedron Lett. 35 (1994) 8019-8022
27. Dess D.B., and Martin J.C. J. Am. Chem. Soc. 113 (1991) 7277-7287
28. Chaudhari S.S. Synlett (2000) 278
29. Nicolaou K.C., Mathison C.J.N., and Montagnon T. J. Am. Chem. Soc. 126 (2004) 5192-5201
30. Nicolaou K.C., Baran P.S., and Zhong Y.-L. J. Am. Chem. Soc. 123 (2001) 3183-3185
31. Zhdankin V.V., and Stang P.J. Chem. Rev. 102 (2002) 2523-2584 and references cited therein
32. Arote N.D., Bhalearo D.S., and Akamanchi K.G. Tetrahedron Lett. 48 (2007) 3651-3653
33. -1) ν: 3427, 2227, 1644
34. Jin Z. Nat. Prod. Rep. 24 (2007) 886-905
35. Chapleur Y., Chretien F., Ahmed S.I., and Khaldi M. Curr. Org. Synth. 3 (2006) 341-378
36. Rinner U., and Hudlicky T. Synlett (2005) 365-387
37. Hudlicky T. J. Heterocycl. Chem. 37 (2000) 535-539
38. Rateb L., and Den H.H.J. Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem. 16 (1978) 297-300
39. Sekizaki H., Itoh K., Toyota E., and Tanizawa K. Heterocycles 59 (2003) 237-243
40. Oberhauser T.A. J. Org. Chem. 62 (1997) 4504-4506
41. Cacioli P., and Reiss J. Aust. J. Chem. 37 (1984) 2525-2535