I2O5: mild and efficient reagents for the oxidation of alcohols in water

Tetrahedron Letters

Volumn 48, Issue 17, 2007, Pages 3017-3019

  Liu, Zhong Quan ^a   Zhao, Yankai ^a   Luo, Haiqing ^a   Chai, Lingzhi ^a   Sheng, Qiuju ^a  

^a GANNAN NORMAL UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL; DIIODE PENTAOXIDE; OXIDE; POTASSIUM BROMIDE; UNCLASSIFIED DRUG; WATER;

ARTICLE; CATALYSIS; CHEMICAL ANALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; ELECTRON; OXIDATION; ROOM TEMPERATURE;

EID: 33947604180     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2007.02.123     Document Type: Article

References (29)

1. Hudlicky M. Oxidations in Organic Chemistry (1990), American Chemical Society, Washington, DC
2. For reviews, see:. Stang P.J., and Zhdankin V.V. Chem. Rev. 96 (1996) 1123
3. Zhdankin V.V., and Stang P.J. Chem. Rev. 102 (2002) 2523
4. Varvoglis A. Hypervalent Iodine in Organic Synthesis (1997), Academic Press, San Diego
5. Wirth T., and Hirt U.H. Synthesis (1999) 1271
6. Stang P.J. J. Org. Chem. 68 (2003) 2997
7. Tohma H., and Kita Y. Adv. Synth. Catal. 346 (2004) 111
8. Wirth T. Angew. Chem. 117 (2005) 3722
9. Angew. Chem., Int. Ed. 44 (2005) 3656
10. Dess D.B., and Martin J.C. J. Org. Chem. 48 (1983) 4155
11. Dess D.B., and Martin J.C. J. Am. Chem. Soc. 113 (1991) 7277
12. Wirth T. Angew. Chem. 113 (2001) 2893
13. Angew. Chem., Int. Ed. 40 (2001) 2812
14. More J.D., and Finney N.S. Org. Lett. 4 (2002) 3001
15. Liu Z., Chen Z.C., and Zheng Q.G. Org. Lett. 5 (2003) 3321
16. Surendra K., Krishnaveni N.S., Reddy M.A., Nageswar Y.V.D., and Rao K.R. J. Org. Chem. 68 (2003) 2058
17. Weik S., Nicholson G., Jung G., and Rademann J. Angew. Chem. 113 (2001) 1489
18. Angew. Chem., Int. Ed. 40 (2001) 1436
19. For selected examples, see: Hiroto, U.; Keiji, N.; Katsumi, O.; Patent No. JP 06040710; Chem. Abstr. 1994, 120 326849.
20. Chandrasekhar S., and Gopalaiah K. Tetrahedron Lett. 43 (2002) 4023
21. Hashemi M.M., Rahimi A., Jaberi Z.K., and Ahmadibeni Y. Acta Chim. Slov. 52 (2005) 86
22. Nicolaou K.C., Montagnon T., and Baran P.S. Angew. Chem. 114 (2002) 1444
23. Angew. Chem., Int. Ed. 41 (2002) 1386
24. Miller R.A., and Hoerrner R.S. Org. Lett. 5 (2003) 285
25. Tohma H., Takizawa S., Maegawa T., and Kita Y. Angew. Chem. 112 (2000) 1362
26. Angew. Chem., Int. Ed. 39 (2000) 1306
27. Tohma H., Maegawa T., Takizawa S., and Kita Y. Adv. Synth. Catal. 344 (2002) 328
28. Chai L.Z., Zhao Y.K., Sheng Q.J., and Liu Z.Q. Tetrahedron Lett. 47 (2006) 9283
29. 1H NMR. The conversion and selectivity were determined by GC-MS.