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C. X. Miao J. Q. Wang B. Yu W. G. Cheng J. Sun S. Chanfreu L. N. He S. J. Zhang Chem. Commun. 2011 47 2697-2699.
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He, L.N.7
Zhang, S.J.8
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36
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85032753528
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The synthesis of NCN pincer complex 1 was improved by modifying the amount of NBS (8 equiv.) and the reaction time (31 h) of the first step of its preparation, the bromination of methyl 3,5-dimethylbenzoate. In addition, the work-up of the second step was also modified. For more details see ESI
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The synthesis of NCN pincer complex 1 was improved by modifying the amount of NBS (8 equiv.) and the reaction time (31 h) of the first step of its preparation, the bromination of methyl 3,5-dimethylbenzoate. In addition, the work-up of the second step was also modified. For more details see ESI.
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40
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2942717047
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Sodium borohydride reduction of deoxybenzoin and benzoin provided 1,2-diphenylethanol and 1,2-diphenylethane-1,2-diol, respectively. See
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Sodium borohydride reduction of deoxybenzoin and benzoin provided 1,2-diphenylethanol and 1,2-diphenylethane-1,2-diol, respectively. See: M. Nakatsuji Y. Hata T. Fujihara K. Yamamoto M. Sasaki H. Takekuma M. Yoshihara T. Minematsu S. Takekuma Tetrahedron 2004 60 5983-6000.
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Tetrahedron
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Nakatsuji, M.1
Hata, Y.2
Fujihara, T.3
Yamamoto, K.4
Sasaki, M.5
Takekuma, H.6
Yoshihara, M.7
Minematsu, T.8
Takekuma, S.9
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41
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77954349337
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Diethyl ether was added to the reaction mixture and then it was cooled to −78 °C, and layers decanted. For more details, see
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Diethyl ether was added to the reaction mixture and then it was cooled to −78 °C, and layers decanted. For more details, see: C. Chandrasekhar N. K. Reddy V. P. Kumar Tetrahedron Lett. 2010 51 3623-3625.
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(2010)
Tetrahedron Lett.
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, pp. 3623-3625
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Chandrasekhar, C.1
Reddy, N.K.2
Kumar, V.P.3
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52
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67649236206
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M. Navarro A. Escobar V. R. Landaeta G. Visbal F. Lopez-Linares M. L. Luis A. Fuentes Appl. Catal., A 2009 363 27-31.
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(2009)
Appl. Catal., A
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Navarro, M.1
Escobar, A.2
Landaeta, V.R.3
Visbal, G.4
Lopez-Linares, F.5
Luis, M.L.6
Fuentes, A.7
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