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Copyright (c) 2014 Pengmian Huang1, Wenjuan Tang3, Guishan Tan1, Wenbin Zeng1, Yuanjian Li1, Qinghua Zhang2, Bo Chen2
This work is licensed under a Creative Commons Attribution 4.0 International License.
Chemoselective Reduction of Carbonyl Compounds to Alcohols with Co-Doped Ammonia Borane
Corresponding Author(s) : Pengmian Huang1
Asian Journal of Chemistry,
Vol. 26 No. 23 (2014)
Abstract
Chemoselective reduction of various carbonyl compounds to alcohols with Co-doped ammonia borane was investigated in the present work. It was observed that Co-doped ammonia borane exhibited much better performance than ammonia borane. The Co-based catalysts could be reused up to four times with a slight decrease in activity. Thus, a mild and efficient method for chemoselective reduction of carbonyl compounds with Co-doped ammonia borane was established. The Co-doped ammonia borane sample was characterized by electron paramagnetic resonance. Electron paramagnetic resonance characterization revealed that Co element in a partially reduced state.
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- W. Li, G. Wu, Y. Chua, Y.P. Feng and P. Chen, Inorg. Chem., 51, 76 (2012).
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- X. Yang, T. Fox and H. Berke, Tetrahedron, 67, 7121 (2011).
- H. Dong and H. Berke, J. Organomet. Chem., 696, 1803 (2011).
- S.E. Denmark and G.L. Beutner, Angew. Chem. Int. Ed., 47, 1560 (2008).
- E. Hayashi, E. Iwamatsu, M. Elias Biswas, Y. Sanada, S. Ahmed, H. Hamid and T. Yoneda, Appl. Catal. A Gen., 179, 203 (1999).
- M. Bhaduri and P.C.H. Mitchell, J. Catal., 77, 132 (1982).
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References
G. Wolf, J. Baumann, F. Baitalow and F.P. Hoffmann, Thermochim. Acta, 343, 19 (2000).
A.D. Sutton, A.K. Burrell, D.A. Dixon, E.B. Garner, J.C. Gordon, T. Nakagawa, K.C. Ott, J.P. Robinson and M. Vasiliu, Science, 331, 1426 (2011).
A. Staubitz, A.P.M. Robertson, M.E. Sloan and I. Manners, Chem. Rev., 110, 4023 (2010).
Z. Tang, X. Chen, H. Chen, L. Wu and X. Yu, Angew. Chem. Int. Ed., 52, 5832 (2013).
H. Inoue, T. Yamazaki, T. Kitamura, M. Shimada, M. Chiku and E. Higuchi, Electrochim. Acta, 82, 392 (2012).
W. Li, G. Wu, Y. Chua, Y.P. Feng and P. Chen, Inorg. Chem., 51, 76 (2012).
S.K. Kim, H. Cho, M.J. Kim, H. Lee, J. Park, Y. Lee, H.C. Kim, C.W. Yoon, S.W. Nam and S.O. Kang, J. Mater. Chem. A, 1, 1976 (2013).
R. Kumar and B.R. Jagirdar, Inorg. Chem., 52, 28 (2013).
S. Karahan, M. Zahmakiran and S. Özkar, Chem. Commun., 48, 1180 (2012).
D. Sun, V. Mazumder, O. Metin and S. Sun, ACS Nano, 5, 6458 (2011).
Z. Xiong, Y. Chua, G. Wu, L. Wang, M.W. Wong, Z.M. Kam, T. Autrey, T. Kemmitt and P. Chen, Dalton Trans., 39, 720 (2009).
X. Yang, T. Fox and H. Berke, Tetrahedron, 67, 7121 (2011).
H. Dong and H. Berke, J. Organomet. Chem., 696, 1803 (2011).
S.E. Denmark and G.L. Beutner, Angew. Chem. Int. Ed., 47, 1560 (2008).
E. Hayashi, E. Iwamatsu, M. Elias Biswas, Y. Sanada, S. Ahmed, H. Hamid and T. Yoneda, Appl. Catal. A Gen., 179, 203 (1999).
M. Bhaduri and P.C.H. Mitchell, J. Catal., 77, 132 (1982).
P.V. Ramachandran and P.D. Gagare, Inorg. Chem., 46, 7810 (2007).