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22
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For contributions of other groups to the Heck reaction of alkenyl nonaflates see: (a) Voigt, K.; von Zezschwitz, P.; Rosauer, K.; Lansky, A.; Adams, A.; Reiser, O.; de Meijere, A. Eur. J. Org. Chem. 1998, 1521.
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28
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33750512355
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note
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4 (292.2): C, 65.77; H, 8.62. Found: C, 65.18; H, 8.53.
-
-
-
-
30
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33750504985
-
-
note
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2 (242.3): C, 79.31; H, 7.49. Found: C, 79.15; H, 7.59.
-
-
-
-
31
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33750526862
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-
note
-
The two diastereomers were clearly separated by GC with a chiral column since the meso-compound gave only one peak, whereas the racemate clearly showed two peaks. Conditions: Chiraldex Gamma Cyclodextrin phase: G-TA (trifluoroacetylcyclodextrine) 30 m × 0.32 mm, flow: 1.2 mL/min; program: start 40 °C in 50° steps to 180 °C, 10 min hold, to 200 °C in 50° steps, 2 min hold. Retention times 11.35 min (meso-9), 13.35 min and 13.47 min (rac-9).
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-
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32
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33750525508
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Dissertation; Freie Universität Berlin, Germany
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(a) Högermeier, J. Dissertation; Freie Universität Berlin, Germany, 2006.
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Högermeier, J.1
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36
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33750511925
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note
-
(e) For desymmetrization of a meso-ketone via nonaflate see also ref. 1e.
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-
-
-
39
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0034058306
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41
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0035544084
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(c) Hodgson, D. M.; Maxwell, C. R.; Wisedale, R.; Matthews, I. R.; Carpenter, K. J.; Dickenson, A. H.; Wonnacott, S. J. Chem. Soc., Perkin Trans. 1 2001, 3150.
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Dickenson, A.H.6
Wonnacott, S.7
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42
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0342948833
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0343457949
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0033603593
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45
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0036532565
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(a) The required boronic acid was synthesized according to: Bouillon, A.; Lancelot, J.-C.; Collot, V.; Bovy, P. R.; Rault, S. Tetrahedron 2002, 58, 2885.
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0037244546
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(b) For a review on heteroaryl boronic acid synthesis, see: Tyrrell, E.; Brookes, P. Synthesis 2004, 469.
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