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Seppelt, M.2
Beck, T.3
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112
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0036458623
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K. Funabiki, N. Nagamori, M. Matsui, D. Enders, Synthesis 2002, 2585
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(2002)
Synthesis
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Funabiki, K.1
Nagamori, N.2
Matsui, M.3
Enders, D.4
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61949457358
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J. Gawronski, N. Wascinska, J. Gajewy, Chem. Rev. 2008, 108, 5227.
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Gawronski, J.1
Wascinska, N.2
Gajewy, J.3
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115
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33846821373
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The imine with a benzyl protecting group shows a base-catalyzed 1,3-proton shift to give N-benzylidene-2,2,2-trifluoro-1-phenylethanamine as product:,. In the presence of TMSCN no addition occurs, the isomer was obtained with 32% ee
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The imine with a benzyl protecting group shows a base-catalyzed 1,3-proton shift to give N-benzylidene-2,2,2-trifluoro-1-phenylethanamine as product:, V. A. Soloshonok, M. Yasumoto, J. Fluorine Chem. 2007, 128, 170. In the presence of TMSCN no addition occurs, the isomer was obtained with 32% ee.
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(2007)
J. Fluorine Chem.
, vol.128
, pp. 170
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Soloshonok, V.A.1
Yasumoto, M.2
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116
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78650408459
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RWTH University, unpublished results
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G. Raabe, S. Wehrse, RWTH University, unpublished results.
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Raabe, G.1
Wehrse, S.2
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117
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78650394170
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CCDC 790750 contains the supplementary crystallographic data for the amino nitrile 2a reported in this communication. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via or on application to CCDC, 12 Union Road, Cambridge CB2 1 EZ, UK [fax.: +44-1223/336-033; e-mail: deposit@ ccdc.cam.ac.uk]
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CCDC 790750 contains the supplementary crystallographic data for the amino nitrile 2a reported in this communication. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via or on application to CCDC, 12 Union Road, Cambridge CB2 1 EZ, UK [fax.: +44-1223/336-033; e-mail: deposit@ ccdc.cam.ac.uk].
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