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North, M.1
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34547798449
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North, M.6
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Chen S.-K., Peng D., Zhou H., Wang L.-W., Chen F.-X., and Feng X. Eur. J. Org. Chem. (2007) 639-644
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23
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34948878544
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21744452286
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Chinchilla, R.1
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Yus, M.5
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32
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39149118982
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note
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1H NMR (300 MHz) spectroscopy.
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33
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27644433855
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note
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Chiral HPLC: Chiralcel OD-H, λ = 210 nm, hexane-2-propanol 99:1, 1.0 mL/min; Chiralcel OG, λ = 210 nm, hexane-2-propanol 99:1, 1.0 mL/min; Chiralpak AD, λ = 210 nm, hexane-2-propanol 99:1, 1.0 mL/min. Chiral GLC: Cyclosil-B, initial temperature 105 °C, flow rate 2.0 °C/min, 9 psi. Racemic samples were prepared in the absence of 2a: Baeza, A.; Nájera, C.; de Gracia Retamosa, M.; Sansano, J. M. Synlett 2005, 2787-2797.
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34
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39149131102
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note
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The (R)-stereochemistry was assigned by the order of elution of the corresponding enantiomers in chiral HPLC according to the literature (Refs. 2b and 12).
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35
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0042812083
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Baeza A., Casas J., Nájera C., Sansano J.M., and Saá J.M. Angew. Chem., Int. Ed. 42 (2003) 3143-3146
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(2003)
Angew. Chem., Int. Ed.
, vol.42
, pp. 3143-3146
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Baeza, A.1
Casas, J.2
Nájera, C.3
Sansano, J.M.4
Saá, J.M.5
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