Synthesis of pillar[n]arenes (n = 5 and 6) with deep eutectic solvent choline chloride 2FeCl3

RSC Advances

Volumn 5, Issue 13, 2015, Pages 9993-9996

  Cao, Jin ^a   Shang, Yuhan ^a   Qi, Bin ^a   Sun, Xuzhuo ^b   Zhang, Lei ^a   Liu, Huiwen ^a   Zhang, Haibo ^a   Zhou, Xiaohai ^a  

^a WUHAN UNIVERSITY   (China)

^b HENAN UNIVERSITY OF TECHNOLOGY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ACETAL RESINS; AROMATIC HYDROCARBONS; CYCLIZATION; ELECTRON SPIN RESONANCE SPECTROSCOPY; EUTECTICS; FREE RADICALS; IRON COMPOUNDS; MAGNETIC MOMENTS; REACTION INTERMEDIATES;

CHOLINE CHLORIDE; CYCLIZATION REACTIONS; DEEP EUTECTIC SOLVENTS; HIGH SELECTIVITY; OPTIMAL CONDITIONS; PARAFORMALDEHYDES; REACTION MECHANISM; X-BAND ELECTRON SPIN RESONANCES;

CHLORINE COMPOUNDS;

EID: 84921317219     PISSN: None     EISSN: 20462069     Source Type: Journal    
DOI: 10.1039/c4ra15758c     Document Type: Article

References (23)

1. Q. Zhang, K. D. Vigier, S. Royer and F. Jerome, Chem. Soc. Rev., 2012, 41, 7108-7146.
2. A. P. Abbott, G. Capper, D. L. Davies, H. Munro, R. K. Rasheed and V. Tambyrajah, Chem. Commun., 2001, 2010-2011.
3. A. P. Abbott, G. Capper, D. L. Davies, R. K. Rasheed and V. Tambyrajah, Green Chem., 2002, 4, 24-26.
4. A. P. Abbott, T. J. Bell, S. Handa and B. Stoddart, Green Chem., 2005, 7, 705-707.
5. S. T. Disale, S. R. Kale, S. S. Kahandal, T. G. Srinivasan and R. V. Jayaram, Tetrahedron Lett., 2012, 53, 2277-2279.
6. Y. Yang, W. He, C. Jia, Y. Ma, X. Zhang and B. Feng, J. Mol. Catal. A: Chem., 2012, 357, 39-43.
7. (a) P. J. Cragg and K. Sharma, Chem. Soc. Rev., 2012, 41, 597-607;
8. (b) H. Zhang and Y. Zhao, Chem.-Eur. J., 2013, 19, 16862-16879.
9. (a) T. Ogoshi, S. Kanai, S. Fujinami, T. Yamagishi and Y. Nakamoto, J. Am. Chem. Soc., 2008, 130, 5022-5023;
10. (b) T. Ogoshi, T. Aoki, K. Kitajima, S. Fujinami, T. Yamagishi and Y. Nakamoto, J. Org. Chem., 2011, 76, 328-331;
11. (c) T. Ogoshi, N. Ueshima, T. Akutsu, D. Yamafuji, T. Furuta, F. Sakakibara and T. i. Yamagishia, Chem. Commun., 2014, 50, 5774-5777;
12. (d) X. B. Hu, Z. Chen, L. Chen, L. Zhang, J. L. Hou and Z. T. Li, Chem. Commun., 2012, 48, 10999-11001.
13. T. Ogoshi and T. Yamagishi, Chem. Commun., 2014, 50, 4776-4787.
14. (a) H. Tao, D. Cao, L. Liu, Y. Kou, L. Wang and H. Meier, Sci. China: Chem., 2012, 55, 223-228;
15. (b) L. Liu, D. Cao, Y. Jin, H. Tao, Y. Kou and H. Meier, Org. Biomol. Chem., 2011, 9, 7007-7010.
16. (a) K. Wang, L. L. Tan, D. X. Chen, N. Song, G. Xi, S. X. A. Zhang, C. Li and Y. W. Yang, Org. Biomol. Chem., 2012, 10, 9405-9409;
17. (b) T. Boinski and A. Szumna, Tetrahedron, 2012, 68, 9419-9422;
18. (c) C. Han, F. Ma, Z. Zhang, B. Xia, Y. Yu and F. Huang, Org. Lett., 2010, 12, 4360-4363.
19. D. Cao, Y. Kou, J. Liang, Z. Chen, L. Wang and H. Meier, Angew. Chem., Int. Ed., 2009, 48, 9721-9723.
20. (a) Y. Ma, Z. Zhang, X. Ji, C. Han, J. He, Z. Abliz, W. Chen and F. Huang, Eur. J. Org. Chem., 2011, 5331-5335;
21. (b) M. Holler, N. Allenbach, J. Sonet and J. F. Nierengarten, Chem. Commun., 2012, 48, 2576-2578.
22. A. P. Abbott, G. Capper, D. L. Davies and R. Rasheed, Inorg. Chem., 2004, 43, 3447-3452.
23. P. Paduraru, R. Popoff, R. Nair, R. Gries, G. Gries and E. Plettner, J. Comb. Chem., 2008, 10, 123-134.