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1
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1642486447
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54349091198
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11
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d) M. Massacret, R. Lakhmiri, P. Lhoste, C. Nguefack, F. B. B. Abdelouahab, R. Fadel, D. Sinou, Tetrahedron: Asymmetry 2000, 11, 3561-3568;
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16
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34250662295
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This work will be published elsewhere
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This work will be published elsewhere.
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18
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0013144515
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F. S. Gibson, M. Sook Park, H. Rapoport, J. Org. Chem. 1994, 59, 7503-7507.
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Gibson, F.S.1
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Rapoport, H.3
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19
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34250689156
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When stoichiometric amounts of 2 were used, 39% of 10 was isolated along with 48 % of 9.
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When stoichiometric amounts of 2 were used, 39% of 10 was isolated along with 48 % of 9.
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21
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34250640323
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The synthesis of 13a is fully described in the Supporting Information.
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The synthesis of 13a is fully described in the Supporting Information.
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23
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0000560517
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a) K. C. Nicolaou, C. V. C. Prasad, P. K. Somers, C.-K. Hwang, J. Am. Chem. Soc. 1989, 111, 5330-5334;
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24
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33845185491
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b) K. C. Nicolaou, C. V. C. Prasad, P. K. Somers, C.-K. Hwang, J. Am. Chem. Soc. 1989, 111, 5335-5340.
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Hwang, C.-K.4
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25
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34250656598
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The same results were obtained by using anhydrous (±)-CSA
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The same results were obtained by using anhydrous (±)-CSA.
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27
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0027492918
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V. Waagen, I. Hollingster, V. Partali, O. Thorstad, T. Anthonsen, Tetrahedron: Asymmetry 1993, 4, 2265-2274.
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Anthonsen, T.5
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28
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34250665486
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[16] Compound (R)-1b is also commercially available. Eur. J. Org. Chem. 2007, 2114-2120
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[16] Compound (R)-1b is also commercially available. Eur. J. Org. Chem. 2007, 2114-2120
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