Sulfated tungstate catalyzed highly accelerated N-formylation

Tetrahedron Letters

Volumn 53, Issue 26, 2012, Pages 3259-3263

  Pathare, Sagar P ^a   Sawant, Ravindra V ^a   Akamanchi, Krishnacharya G ^a  

^a INSTITUTE OF CHEMICAL TECHNOLOGY   (India)

Author keywords

Amines; Formic acid; Heterogeneous catalysis; N formylation; Sulfated tungstate

Indexed keywords

AMINE; FORMIC ACID; SULFATE; SULFATED TUNGSTATE; TUNGSTEN DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CATALYST SUPPORT; CHEMICAL MODIFICATION; CONTROLLED STUDY; FORMYLATION; GREEN CHEMISTRY; REACTION OPTIMIZATION; STEREOCHEMISTRY; SULFATION;

EID: 84861528658     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2012.04.058     Document Type: Article

References (38)

1. P.S. Chaudhari, S.D. Salim, R.V. Sawant, and K.G. Akamanchi Green Chem. 12 2010 1707
2. K.V. Katkar, P.S. Chaudhari, and K.G. Akamanchi Green Chem. 13 2011 835
3. S.D. Salim, and K.G. Akamanchi Catal. Commun. 12 2011 1153
4. S.D. Salim, S.P. Pathare, and K.G. Akamanchi Catal. Commun. 13 2011 78
5. S.P. Pathare, and K.G. Akamanchi Tetrahedron Lett. 53 2012 871
6. A. Jackson, and O. Meth-Cohn J. Chem. Soc., Chem. Commun. 1995 1319
7. K. Kobayashi, S. Nagato, M. Kawakita, O. Morikawa, and H. Konishi Chem. Lett. 1995 575
8. A. Kakehi, S. Ito, S. Hayashi, and T. Fujii Bull. Chem. Soc. Jpn. 68 1995 3573
9. B.B. Lohray, S. Baskaran, B.S. Rao, B.Y. Reddy, and I.N. Rao Tetrahedron Lett. 40 1999 4855
10. S. Kobayashi, M. Yasuda, and I. Hachiya Chem. Lett. 1996 407
11. K. Iseki, S. Mizuno, Y. Kuroki, and Y. Kobayashi Tetrahedron 55 1999 977
12. Y. Han, and L. Cai Tetrahedron Lett. 38 1997 5423
13. F. Effenberger, and J. Eichhorn Tetrahedron: Asymmetry 8 1997 469
14. U. Schollkopf Angew. Chem., Int. Ed. Engl. 16 1977 339
15. L.G. Humer, F. Herr, and M.P. Charest J. Med. Chem. 14 1971 982
16. J. Martinez, and J. Laur Synthesis 1982 979
17. A. Floresheimer, and M.R. Kula Monatsh. Chem. 119 1988 1323
18. F.F. Blicke, and C.J. Lu J. Am. Chem. Soc. 74 1952 3933
19. J. Waki, and J. Meinhofer J. Org. Chem. 42 1977 2019
20. F.M.F. Chen, and N.L. Benoiton Synthesis 1979 709
21. L.D. Luca, G. Giacomelli, A. Porcheddu, and M. Salaris Synlett 2004 2570
22. W. Duezek, J. Deutsch, S. Vieth, and H.J. Niclas Synthesis 1996 37
23. T.W. Green, and P.G.M. Wuts Protective Groups in Organic Synthesis 3rd ed. 1999 Wiley-Interscience New York 116
24. J.C. Sheehan, and D.D.H. Yang J. Am. Chem. Soc. 80 1958 1154
25. P. Strazzolini, A.G. Giumanini, and S. Cauci Tetrahedron 46 1990 1081
26. P.G. Reddy, G.D.K. Kumar, and S. Bhaskaran Tetrahedron 41 2000 9149
27. G. Brahmachari, and S. Laskar Tetrahedron Lett. 51 2010 2319
28. B. Das, M. Krishnaiah, P. Balasubramanyam, B. Veeranjaneyulu, and D. Nandakumar Tetrahedron Lett. 49 2008 2225
29. A. Chandra Shekhar, A. Ravi Kumar, G. Sathaiah, V. Luke Paul, M. Sridhar, and P. Shanthan Rao Tetrahedron Lett. 50 2009 7099
30. M. Mihara, Y. Ishino, S. Minakara, and M. Komatsu Synthesis 2003 2317
31. B. Krishnakumar, and M. Swaminathan J. Mol. Catal. A: Chem. 334 2011 98
32. M. Bhojegowd, A. Nizam, and M. Pasha Chin. J. Catal. 31 2010 518
33. J.G. Kim, and D.O. Jang Synlett 2010 1231
34. J.G. Kim, and D.O. Jang Synlett 2010 2093
35. M. Hosseini-Sarvari, and H. Sharghi J. Org. Chem. 71 2006 6652
36. L. Mamani, M. Sheykhan, A. Heydari, M. Faraji, and Y. Yamini Appl. Catal., A 377 2010 64
37. J.G. Kim, and D.O. Jang Synlett 2010 1231
38. C.J.K. Paul, C.C. Marco, J.M.N. Roeland, H. Tadao, M.F.H. Alphons, and D. Wiendelt J. Am. Chem. Soc. 110 1988 1581