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A part of the results in this article has been reported as a preliminary letter:
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A part of the results in this article has been reported as a preliminary letter:. Hirasawa S., Nagano H., and Kameda K. Tetrahedron Lett. 45 (2004) 2207-2209
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34648829465
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It has been reported that aryl acrylates react much faster than their alkyl counterparts in the Baylis-Hillman reactions.
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23
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1642306315
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For the chelation-controlled stereoselective catalytic hydrogenation of γ-hydroxy-α-methylene carboxylic acid esters, see:
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For the chelation-controlled stereoselective catalytic hydrogenation of γ-hydroxy-α-methylene carboxylic acid esters, see:. Nagano H., Yokota M., and Iwazaki Y. Tetrahedron Lett. 45 (2004) 3035-3037
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24
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34648817816
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note
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No reduction of alkyl acrylates was observed under the reaction conditions.
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25
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34648814672
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For conjugate reductions of α,β-unsaturated esters with metal hydrides other than tin hydrides, see:
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34648820892
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note
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The chelation-controlled diastereoselective radical addition and reduction reactions of γ-substituted α-methylene-γ-butyrolactams will be reported elsewhere.
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