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For recent alternative methods of the preparation of optically enriched a-substituted allylic boronates, see: a X. Gao, D. G. Hall, J. Am. Chem. Soc. 2003, 125, 9308-9309;
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For recent alternative methods of the preparation of optically enriched a-substituted allylic boronates, see: a) X. Gao, D. G. Hall, J. Am. Chem. Soc. 2003, 125, 9308-9309;
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For the simple two-step synthesis of 6 from 3-chloropropyne, see: M. Gravel, B. B. Touré, D. G. Hall, Org. Prep. Proced. Int. 2004, 36, 573-579.
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For the simple two-step synthesis of 6 from 3-chloropropyne, see: M. Gravel, B. B. Touré, D. G. Hall, Org. Prep. Proced. Int. 2004, 36, 573-579.
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34547793630
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The uncatalyzed reaction gives a 3:1 E/Z selectivity.
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The uncatalyzed reaction gives a 3:1 E/Z selectivity.
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33
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34547800732
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3 was necessary for a high E/Z ratio.
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3 was necessary for a high E/Z ratio.
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0037594874
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For a phase-transfer-catalysis approach using chiral ammonium salts, in which no enantioselectivity was observed, see
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For a phase-transfer-catalysis approach using chiral ammonium salts, in which no enantioselectivity was observed, see: A. N. Thadani, R. A. Batey, Org. Lett. 2002, 4, 3827-3830.
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