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a) A. L. Sabb, R. L. Vogel, G. P. Stack, D. A. Evrard, A. A. Failli, L. Krishnan, A. W. Chan, J. Ren, C. Guinosso, R. B. Baudy, J. Y.-C. Sze, Y. Li, C. J. Stanton III, A. Nikitenko, Patent WO 2006089053, 2006;
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(2006)
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Sabb, A.L.1
Vogel, R.L.2
Stack, G.P.3
Evrard, D.A.4
Failli, A.A.5
Krishnan, L.6
Chan, A.W.7
Ren, J.8
Guinosso, C.9
Baudy, R.B.10
Sze, J.Y.-C.11
Li, Y.12
Stanton III, C.J.13
Nikitenko, A.14
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87
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38949128649
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and references therein
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b) A. Nikitenko, D. Evrard, A. L. Sabb, R. L. Vogel, G. Stack, M. Young, M. Lin, B. L. Harrison, J. R. Potoski, Org. Process Res. Dev. 2008, 12, 76-80, and references therein.
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(2008)
Org. Process Res. Dev.
, vol.12
, pp. 76-80
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Nikitenko, A.1
Evrard, D.2
Sabb, A.L.3
Vogel, R.L.4
Stack, G.5
Young, M.6
Lin, M.7
Harrison, B.L.8
Potoski, J.R.9
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88
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79952542388
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CCDC 714947 (3m) and 714948 (5) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
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CCDC 714947 (3m) and 714948 (5) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data- request/cif.
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89
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77952356805
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During the preparation of this manuscript, Zhao et al reported a Diels-Alder reaction between 2-vinylindoles and enals by using chiral diarylprolinols, see: However, 2-vinylindoles of this study are not applicable in their catalyst system as poor stereoselectivities were observed
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During the preparation of this manuscript, Zhao et al reported a Diels-Alder reaction between 2-vinylindoles and enals by using chiral diarylprolinols, see: C.-G. Zheng, Y.-P. Lu, J.-K. Zhang, X.-K. Chen, Z. Chai, W.-Y. Ma, G. Zhao, Chem. Eur. J. 2010, 16, 5853-5857. However, 2-vinylindoles of this study are not applicable in their catalyst system as poor stereoselectivities were observed.
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(2010)
Chem. Eur. J.
, vol.16
, pp. 5853-5857
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Zheng, C.-G.1
Lu, Y.-P.2
Zhang, J.-K.3
Chen, X.-K.4
Chai, Z.5
Ma, W.-Y.6
Zhao, G.7
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