Synthesis of 6-hydroxy-2-naphthoic acid from 2,6-diisopropylnaphthalene using NHPI as a key catalyst

Tetrahedron

Volumn 65, Issue 18, 2009, Pages 3577-3581

  Nakamura, Ryota ^a   Obora, Yasushi ^a   Ishii, Yasutaka ^a  

^a KANSAI UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

4 HYDROXYBENZOIC ACID; NAPHTHALENE DERIVATIVE;

ARTICLE; CATALYST; CHEMICAL REACTION; CHEMICAL STRUCTURE; DEACETYLATION; ESTERIFICATION; HYDROLYSIS; OXIDATION; PRIORITY JOURNAL; SYNTHESIS;

EID: 63249088027     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2009.03.013     Document Type: Article

References (33)

1. De Ruijter C., Bos J., Boerstoel H., and Dingemans T.J. J. Polym. Sci., Part A: Polym. Chem. 46 (2008) 6565
2. Hsiue L.-T., Ma C.-C.M., and Tsai H.-B. J. Appl. Polym. Sci. 56 (1995) 471
3. Nagata M. High Perform. Polym. 13 (2001) S265
4. Gao P., Lu X.H., and Chai C.K. Polym. Eng. Sci. 36 (1996) 2771
5. Lindsey A.S., and Jeskey H. Chem. Rev. 57 (1957) 583
6. Rahim M.A., Matsui Y., and Kosugi Y. Bull. Chem. Soc. Jpn. 75 (2002) 619
7. Kumagai H., Ueda S., and Hori T. Nippon Kagaku Kaishi (1991) 170
8. Iijima T., Iwase T., and Yamaguchi T. J. Jpn. Pet. Inst. 49 (2006) 206
9. Kolbe H., and Lautemann E. Justus Liebigs Ann. Chem. 113 (1860) 125
10. Schmitt R. J. Prakt. Chem. 31 (1886) 397
11. Minisci F., Recupero F., Fontana F., Bjørsvik H.-R., and Liguori L. Synlett (2002) 610
12. Kantam M.L., Ranganath K.V.S., Sateesh M., Kumar K.B.S., and Choudary B.M. J. Mol. Catal. A: Chem. 225 (2005) 15
13. Melero J.A., van Grieken R., Morales G., and Nuño V. Catal. Commun. 5 (2004) 131
14. Klein C.D.P., Tabeteh G.F., Laguna A.V., Holzgrabe U., and Mohr K. Eur. J. Pharm. Sci. 14 (2001) 167
15. Fukuda O., Sakaguchi S., and Ishii Y. Adv. Synth. Catal. 343 (2001) 809
16. Compound 1:. Serrano-Wu M.H., Regueiro-Ren A., St. Laurent D.R., Carroll T.M., and Balasubramanian B.N. Tetrahedron Lett. 42 (2001) 8593
17. Compound 3:. Zawadiak J., Orlinska B., and Stec Z. Fresenius' J. Anal. Chem. 367 (2000) 502
18. Compound 4:. Huebner C.F., and Jacobs W.A. J. Biol. Chem. 169 (1947) 211
19. Compound 5:. Zoeller J.R., and Sumner C.E. J. Org. Chem. 55 (1990) 319
20. Compound 6:. Gao Y., Voigt J., Zhao H., Pais G.C.G., Zhang X., Wu L., Zhang Z.-Y., and Burke Jr. T.R. J. Med. Chem. 44 (2001) 2869
21. Compound 7:. Aoki Y., Sakaguchi S., and Ishii Y. Adv. Synth. Catal. 346 (2004) 199
22. Compound 8:. Minisci F., Recupero F., Cecchetto A., Gambarotti C., Punta C., Paganelli R., Pedulli G.F., and Fontana F. Org. Process Res. Dev. 8 (2004) 163
23. Compound 10:. Zaccheria F., Ravasio N., Ercoli M., and Allegrini P. Tetrahedron Lett. 46 (2005) 7743
24. Compound 11: Ref. 5d;
25. Compound 12: Shishido, Y.; Nakao, K.; Nagayama, S.; Tanaka, H.; Duncton, M. A. J.; Cox, M.; Kincaid, J.; Sahasrabudhe, K.; Estiarte-Martinez, M. PCT Int. Appl., 2007, WO 2007133637;
26. Compound 13:. Kim H.M., Jung C., Kim B.R., Jung S.-Y., Hong J.H., Ko Y.-G., Lee K.J., and Cho B.R. Angew. Chem., Int. Ed. 46 (2007) 3460
27. Compound 14:. Rajarathnam D., and Nadar P.A. Int. J. Chem. Kinet. 33 (2001) 157
28. Compound 15:. Teoh M.M., Chung T.-S., and Pramoda K.P. Synth. Met. 147 (2004) 191
29. Compound 16:. Kshirsagar V.S., Vijayanand S., Potdar H.S., Joy P.A., Patil K.R., and Rode C.V. Chem. Lett. 37 (2008) 310
30. Compound 18:. Kianmehr E., Yahyaee M., and Tabatabai K. Tetrahedron Lett. 48 (2007) 2713
31. Compound 19:. Lebel H., Davi M., Díez-González S., and Nolan S.P. J. Org. Chem. 72 (2007) 144
32. Compound 20:. Moghadam M., Tangestaninejad S., Mirkhani V., Mohammadpoor-Baltork I., and Taghavi S.A. J. Mol. Catal. A: Chem. 274 (2007) 217
33. Compound 21:. Yeung C.S., and Dong V.M. J. Am. Chem. Soc. 130 (2008) 7826