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Pindur, U.; Lutz, G.; Otto, C. Chem. Rev. 1993, 93, 741.
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Nicolaou, K. C.; Synder, S. A.; Montagnon, T.; Vassilikogiannakis, G. Angew. Chem., Int. Ed. 2002, 41, 1668.
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For some recent development of Diels-Alder type reactions
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Kim, W. H.; Lee, J. H.; Danishefsky, S. J. J. Am. Chem. Soc. 2009, 131, 12576.
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For reviews on the hetero-Diels-Alder reaction
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For reviews on the retro-Diels-Alder reaction
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For reviews on the dehydro-Diels-Alder reaction
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Kolb, H.C.5
Sharpless, K.B.6
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37
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80054775165
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The reaction of 1a in both the presence and absence of radical initiator azobisisobutyronitrile (5 mol %) under the standard conditions provided cycloadduct 2a in the same yields (78%)
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The reaction of 1a in both the presence and absence of radical initiator azobisisobutyronitrile (5 mol %) under the standard conditions provided cycloadduct 2a in the same yields (78%).
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38
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0030018945
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For detailed energy profiles of the reactions and corresponding molecular structures, see Supporting Information
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For detailed energy profiles of the reactions and corresponding molecular structures, see Supporting Information.
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41
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80054741933
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The reaction of deuterium-labeled dieneyne 1a produced 2a with 50% deuterium labeling (vide infra). Therefore, the H/D kinetic isotope effect was not observed
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The reaction of deuterium-labeled dieneyne 1a produced 2a with 50% deuterium labeling (vide infra). Therefore, the H/D kinetic isotope effect was not observed.
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