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85083243520
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For relevant reviews see: a) J. Tsuji, Synthesis 1984, 369-384;
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Tsuji, J.1
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c) R. A. Alonso, C. S. Burgey, B. V. Rao, G. D. Vite, R. Vollerthun, M. A. Zottola, B. Fraser-Reid, J. Am. Chem. Soc. 1993, 115, 6666-6672;
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e) K. H. Jensen, T. P. Pathak, Y. Zhang, M. S. Sigman, J. Am. Chem. Soc. 2009, 131, 17074-17075;
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77953568657
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Michel, B.W.1
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33847085661
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H. Mimoun, R. Charpentier, A. Mitschler, J. Fischer, R.Weiss, J. Am. Chem. Soc. 1980, 102, 1047-1054
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0037155505
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P. N. Collier, A. D. Campbell, I. Patel, T. M. Raynham, R. J. K. Taylor, J. Org. Chem. 2002, 67, 1802-1815
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21
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77957351023
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Due to the poor reactivity and selectivity the retention of enantiomeric excess was not evaluated under Tsuji-Wacker conditions
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Due to the poor reactivity and selectivity the retention of enantiomeric excess was not evaluated under Tsuji-Wacker conditions
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22
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55049126397
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N. Ohmura, A. Nakamura, A. Hamasaki, M. Tokunaga, Eur. J. Org. Chem. 2008, 5042-5045
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Ohmura, N.1
Nakamura, A.2
Hamasaki, A.3
Tokunaga, M.4
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23
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77957328968
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Analysis based on crude 1H NMR integrations. Quantitative analysis proved difficult due to rotomers convoluting 1H NMR spectra and decomposition of the analyte
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Analysis based on crude 1H NMR integrations. Quantitative analysis proved difficult due to rotomers convoluting 1H NMR spectra and decomposition of the analyte
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24
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0037154749
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R. V. Hoffman, N. Maslouh, F. Cervantes-Lee, J. Org. Chem. 2002, 67, 1045-1056
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Hoffman, R.V.1
Maslouh, N.2
Cervantes-Lee, F.3
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25
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77957339909
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For preparation of the [Pd(Quinox)Cl2] complex and full analytical data see Ref. [6]. See the Supporting Information for the one-pot synthesis procedure
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For preparation of the [Pd(Quinox)Cl2] complex and full analytical data see Ref. [6]. See the Supporting Information for the one-pot synthesis procedure
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