Erratum: Expression of concern: Chemoselective hydration of nitriles to amides using hydrated ionic liquid (IL) tetrabutylammonium hydroxide (TBAH) as a green catalyst (RSC Adv. (2015) 5 (6365-6371) DOI: 10.1039/C4RA09864A);Chemoselective hydration of nitriles to amides using hydrated ionic liquid (IL) tetrabutylammonium hydroxide (TBAH) as a green catalyst

RSC Advances

Volumn 5, Issue 9, 2015, Pages 6365-6371

  Veisi, Hojat ^a   Maleki, Behrooz ^b   Hamelian, Mona ^a   Ashrafi, Samaneh Sedigh ^b  

^a PAYAME NOOR UNIVERSITY   (Iran)

^b HAKIM SABZEVARI UNIVERSITY   (Iran)

Author keywords

[No Author keywords available]

Indexed keywords

AMIDES; CYANIDES; IONIC LIQUIDS; TRANSITION METALS;

CHEMOSELECTIVE; GREEN CATALYSTS; HETEROAROMATICS; HIGH IMPACT; METAL FREE; NITRILE GROUPS; REGIO-SELECTIVE; TETRABUTYLAMMONIUM HYDROXIDES;

HYDRATION;

EID: 84920849260     PISSN: None     EISSN: 20462069     Source Type: Journal    
DOI: 10.1039/d4ra90115k     Document Type: Erratum

References (71)

1. N. Z. Burns, P. S. Baran and R. W. Hoffmann, Angew. Chem., Int. Ed., 2009, 48, 2854.
2. V. Y. Kukushkin and A. J. L. Pombeiro, Chem. Rev., 2002, 102, 1771.
3. R. Opsahl, Encyclopedia of Chemical Technology, ed. J. I. Kroschwitz, Wiley, New York, 1991, vol. 2, p. 346.
4. (a) V. Y. Kukushikin and A. J. L. Pombeiro, Inorg. Chim. Acta, 2005, 358, 1;
5. (b) J. N. Moorthy and N. Singhal, J. Org. Chem., 2005, 70, 1926;
6. (c) H. R. Sydner and C. T. Elston, J. Am. Chem. Soc., 1954, 76, 3039;
7. (d) C. R. Hauser and C. J. Eby, J. Am. Chem. Soc., 1957, 79, 725;
8. (e) C. P. Wilgus, S. Downing, E. Molitor, S. Bains, R. M. Pagni and G. W. Kabalka, Tetrahedron Lett., 1995, 36, 3469;
9. (f) L. McMaster and F. B. Langreck, J. Am. Chem. Soc., 1917, 39, 103;
10. (g) N. Kornblum and S. Singaram, J. Org. Chem., 1979, 44, 4727;
11. (h) S. Caochi, D. Misiti and L. F. Torre, Synthesis, 1980, 243;
12. (i) A. R. Katritzky, B. Pilarski and L. Urogdi, Synthesis, 1989, 949.
13. A. Goto, K. Endo and S. Saito, Angew. Chem., Int. Ed., 2008, 47, 3607.
14. (a) T. Oshiki, H. Yamashita, K. Sawada, M. Utsunomiya, K. Takahashi and K. Takai, Organometallics, 2005, 24, 6287;
15. (b) S. C. Ghosh, J. S. Y. Ngiam, A. M. Seayad, D. T. Tuan, C. L. L. Chai and A. Chen, J. Org. Chem., 2012, 77, 8007;
16. (c) E. Bolgy-Nagy, A. Udvardy, F. Joo and A. Katho, Tetrahedron Lett., 2014, 55, 3615;
17. (d) V. Cadierno, J. Francos and J. Gimeno, Chem. - Eur. J., 2008, 14, 6601;
18. (e) R. B. Nasir Baig, M. N. Nadagouda and R. S. Varma, Green Chem., 2014, 16, 2122;
19. (f) E. Tomas-Mendivil, F. J. Suarez, J. Diez and V. Cadierno, Chem. Commun., 2014, 50, 9661;
20. (g) V. Polshettiwar and R. S. Varma, Chem. - Eur. J., 2009, 15, 1582;
21. (h) K. Yamaguchi, M. Matsushita and N. Mizuno, Angew. Chem., 2004, 116, 1602;
22. (i) C. W. Leung, W. Zheng, Z. Zhou, Z. Lin and C. P. Lau, Organometallics, 2008, 27, 4957;
23. (j) C. S. Yi, T. N. Zeczycki and S. V. Lindeman, Organometallics, 2008, 27, 2030.
24. (a) A. Goto, K. Endo and S. Saito, Angew. Chem., 2008, 120, 3663;
25. (b) A. Goto, H. Naka, R. Noyori and S. Saito, Chem. - Asian J., 2011, 6, 1740.
26. T. Tu, Z. Wang, Z. Liu and X. Feng, Green Chem., 2012, 14, 921.
27. P. K. Verma, N. Kumar, U. Sharma, M. Bala, V. Kumar and B. Singh, Synth. Commun., 2013, 43, 2867.
28. R. S. Ramon, N. Marion and S. P. Nolan, Chem. - Eur. J., 2009, 15, 8695.
29. I. N. Stepanenko, B. Cebrin-Losantos, V. B. Arion, A. A. Krokhin, A. A. Nazarov and B. K. Keppler, Eur. J. Inorg. Chem., 2007, 3, 400.
30. X. B. Jiang, A. J. Minnaard, B. L. Feringa and J. G. DeVries, J. Org. Chem., 2004, 69, 2327.
31. (a) E. S. Kim, H. S. Kim and J. N. Kim, Tetrahedron Lett., 2009, 50, 2973;
32. (b) K. I. Shimizu, T. Kubo, A. Satsuma, T. Kamachi and K. Yoshizawa, ACS Catal., 2012, 2, 2467.
33. C. S. Chin, S. Y. Kim, K. S. Joo, G. Won and D. Chong, Bull. Korean Chem. Soc., 1999, 20, 535.
34. (a) K. L. Breno, M. D. Pluth and D. R. Tyler, Organometallics, 2003, 22, 1203;
35. (b) K. L. Breno, M. D. Pluth, C. W. Landorf and D. R. Tyler, Organometallics, 2004, 23, 1738.
36. C. Battilocchio, J. M. Hawkins and S. V. Ley, Org. Lett., 2014, 16, 1060.
37. N. K. Thallaj, J. Przybilla, R. Welter and D. Mandon, J. Am. Chem. Soc., 2008, 130, 2414.
38. P. M. Angus and W. G. Jackson, Inorg. Chem., 1996, 35, 7196.
39. W. Schibler and T. A. Kaden, J. Chem. Soc., Chem. Commun., 1981, 603.
40. (a) K. I. Shimizu, N. Imaiida, K. Sawabe and A. Satsuma, Appl. Catal., A, 2012, 421-422, 114;
41. (b) D. A. Buckingham, B. M. Foxman, A. M. Sargeson and A. Zanella, J. Am. Chem. Soc., 1972, 94, 8246.
42. M. Tamura, H. Wakasugi, K. Shimizu and A. Satsuma, Chem. - Eur. J., 2011, 17, 11428.
43. (a) T. Subramanian and K. Pitchumani, Catal. Commun., 2012, 29, 109;
44. (b) Y. Gangarajula and B. Gopal, Appl. Catal., A, 2014, 475, 211.
45. (a) B. Maleki, S. Hemmati, A. Sedrpoushan, S. Sedigh Ashrafi and H. Veisi, RSC Adv., 2014, 4, 40505;
46. (b) B. Maleki and S. Sedigh Ashrafi, J. Mex. Chem. Soc., 2014, 58, 74;
47. (c) B. Maleki, S. Hemmati, R. Tayebee, S. Salemi, Y. Farokhzad, M. Baghayeri, F. Mohammadi Zonoz, E. Akbarzadeh, R. Moradi, A. Entezari, M. R. Abdi, S. Sedigh Ashrafi, F. Taimazi and M. Hashemi, Helv. Chim. Acta, 2013, 96, 2147;
48. (d) B. Maleki, S. Barzegar, Z. Sepehr, M. Kermanian and R. Tayebee, J. Iran. Chem. Soc., 2012, 9, 757;
49. (e) B. Maleki and F. Taimazi, Org. Prep. Proced. Int., 2014, 46, 252;
50. (f) H. Veisi, A. Khazaei, M. Safaei and D. Kordestani, J. Mol. Catal. A: Chem., 2014, 382, 106;
51. (g) H. Veisi, R. Masti, D. Kordestani, M. Safaei and O. Sahin, J. Mol. Catal. A: Chem., 2014, 385, 61;
52. (h) B. Maleki, S. Sedigh Ashrafi and R. Tayebee, RSC Adv., 2014, 4, 41521;
53. (i) B. Maleki and S. Sedigh Ashrafi, J. Mex. Chem. Soc., 2014, 58, 159;
54. (j) B. Maleki and H. Veisi, Bull. Korean Chem. Soc., 2011, 32, 4366;
55. (k) H. Veisi, B. Maleki, F. Hosseini Eshbala, H. Veisi, R. Masti, S. Sedigh Ashrafi and M. Baghayeri, RSC Adv., 2014, 4, 30683;
56. (l) B. Maleki and S. Sedigh Ashrafi, RSC Adv., 2014, 4, 42873;
57. (m) H. Veisi, A. Maleki, Z. Omrani and S. Lotfi, RSC Adv., 2014, 4, 55313;
58. (n) H. Veisi, M. Hamelian and S. Hemmati, J. Mol. Catal. A: Chem., 2014, 395, 25;
59. (o) M. Baghayeri, H. Veisi, H. Veisi, B. Maleki, H. Karimi-Maleh and H. Beitollahi, RSC Adv., 2014, 4, 49595;
60. (p) M. Gholizadeh, M. Ebrahimpour, S. F. Hojati and B. Maleki, Arabian J. Chem., 2014, 7, 267.
61. (a) H. Veisi, A. Aminimanesh, N. Khankhani and R. Ghorbani-Vaghei, RSC Adv., 2014, 4, 25057;
62. (b) M. A. Zolfigol, A. Khazaei, A. R. Moosavi-Zare, A. Zare, H. G. Kruger, V. Khakyzadeh and M. Kazem-Rostami, J. Org. Chem., 2012, 77, 3640;
63. (c) H. Veisi, A. Sedrpoushan, P. Mohammadi, A. R. Faraji and S. Sajjadifar, RSC Adv., 2014, 4, 25898;
64. (d) R. Gusain, R. Singh, K. L. N. Sivakumar and O. P. Khatri, RSC Adv., 2014, 4, 1293;
65. (e) Y. Zhang, A. Zhu, Q. Li, L. Li, Y. Zhao and J. Wang, RSC Adv., 2014, 4, 22946;
66. (f) K. C. Lethesh, W. Dehaen and K. Binnemans, RSC Adv., 2014, 4, 4472;
67. (g) A. Brandt, J. Gräsvik, J. P. Halletta and T. Welton, Green Chem., 2013, 15, 550;
68. (h) L. L. Dong, L. He, G. H. Tao and C. w. Hu, RSC Adv., 2013, 3, 4806;
69. (i) A. Zhu, S. Bai, W. Jin, R. Liu, L. Li, Y. Zhao and J. Wang, RSC Adv., 2014, 4, 36031;
70. (j) H. Otaka, J. Ikeda, D. Tanaka and M. Tobe, Tetrahedron Lett., 2014, 55, 979;
71. (k) A. Khazaei, H. Veisi, M. Safaei and H. Ahmadian, J. Sulfur Chem., 2014, 35, 270.