[MeC(OH) 2] +ClO 4 -: A new efficient organocatalyst for the preparation of 1-amido- and 1-carbamato-alkyl naphthols

Synlett

Volumn , Issue 20, 2011, Pages 2947-2950

  Tamaddon, Fatemeh ^a   Bistgani, Javad Moazeni ^a  

^a YAZD UNIVERSITY   (Iran)

Author keywords

amidoalkyl naphthols; ionic liquids; multicomponent reactions; super acids

Indexed keywords

1 AMIDO ALKYLNAPHTHOL DERIVATIVE; 1 CARBAMATO ALKYLNAPHTHOL DERIVATIVE; 2 NAPHTHOL; ALDEHYDE DERIVATIVE; AMIDE; CARBAMIC ACID DERIVATIVE; IONIC LIQUID; NAPHTHOL DERIVATIVE; NITRILE; UNCLASSIFIED DRUG;

ARTICLE; CATALYST; CHEMICAL REACTION; CONDENSATION; DRUG SYNTHESIS; PROCESS OPTIMIZATION; REACTION TIME;

EID: 82955237239     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0031-1289906     Document Type: Article

References (33)

1. Hobbs H R., Thomas N R., Chem. Rev. 2007 107 2786
2. Shen A Y., Tsai C T., Chen C L., Eur. J. Med. Chem. 1999 877
3. Damodiran M, Selvam N P., Perumal P T., Tetrahedron Lett. 2009 50 5474
4. Johnson P Y., Silver R B., J. Heterocycl. Chem. 1973 10 1029
5. Haneishi T, Okazaki T, Hata T, Tamura C, Nomura M, Naito A, Seki I, Arai M, J. Antibiotics 1971 24 797
6. Lesher G Y., Surrey A R., J. Am. Chem. Soc. 1955 77 636
7. Matsuoka H, Ohi N, Mihara M, Suzuki H, Miyamoto K, Maruyama N, Tsuji K, Kato N, Akimoto T, Takeda Y, Yano K, Kuroki T, J. Med. Chem. 1997 40 105
8. Ren H, Grady S, Gamenara D, Heinzen H, Moyna P, Croft S, Kendrick H, Yardley V, Moyna G, Bioorg. Med. Chem. Lett. 2001 11 1851
9. Khodaei M M., Khosropour A R., Moghanian H, Synlett 2006 916
10. Das B, Laxminarayana K, Ravikanth B, Rao B R., J. Mol. Catal. A: Chem. 2007 261 180
11. Szatmari I, Fulop F, Synthesis 2009 775
12. Patil S B., Singh P R., Surpur M P., Samant S D., Ultrason. Sonochem. 2007 14 515
13. Shaterian H R., Yarahmadi H, Tetrahedron Lett. 2008 49 1297
14. Das B, Laxminarayana K, Thirupathi P, Ramarao B, Synlett 2007 3103
15. Rashinkar G, Salunkhe R, J. Mol. Catal. A: Chem. 2010 316 146
16. Kunda D, Majee A, Hajra A, Catal. Commun. 2010 11 1157
17. Zhang Q, Luo J, Wei Y, Green Chem. 2010 12 2246
18. Foroughifar N, Mobinikhaledi A, Moghanian H, Ebrahimi S, BodaghiFard M A., Synlett 2008 821
19. Nandi G C., Samai S, Kumar R, Singh M S., Tetrahedron Lett. 2009 50 7220
20. Niralwad K S., Shingate B B., Shingare M S., Chin. Chem. Lett. 2011 22 551
21. Hall N F., Conant J B., J. Am. Chem. Soc. 1927 49 3047
22. Conant J B., Hall N F., J. Am. Chem. Soc. 1927 49 3062
23. Matsumoto K, Tetrahedron 1968 24 6851
24. Tamaddon F, Amrollahi M A., Sharafat L, Tetrahedron Lett. 2005 46 7841
25. Tamaddon F, Khoobi M, Keshavarz E, Tetrahedron Lett. 2007 48 3643
26. Tamaddon F, Nasiri A, Farokhi S, Catal. Commun. 2011 12 1477
27. Tamaddon, F.; Tavakoli, F. manuscript submitted for publication.
28. Tamaddon F, Tavakoli F, J. Mol. Catal. A: Chem. 2011 337 52
29. Bamoharram F F., Heravi M M., Roshani M, SaneCharkhi M J., E.-J. Chem. 2011 8 523
30. An L T., Lu X H., Ding F Q., Jiang W Q., Zou J P., Chin. J. Chem. 2008 26 2117
31. Wang M, Liang Y, Monatsh. Chem. 2010 142 153
32. Shaterian H R., Hosseinian A, Ghashang M, Tetrahedron Lett. 2008 49 5804
33. Hajipour A R., Ghayeb Y, Sheikhan N, Ruoho A E., Tetrahedron Lett. 2009 50 5649