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note
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1H NMR spectroscopy. The crude product was purified by column chromatography (1:1 EtOAc/petroleum spirits) to afford the pure product in the yield stated.
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77
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77957812960
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See Supplementary data for temperature, pressure, and power profiles for this reaction
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See Supplementary data for temperature, pressure, and power profiles for this reaction.
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78
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0000152667
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For the reaction of quadricyclane with DMAD, see: C.D. Smith J. Am. Chem. Soc. 88 1966 4273 4274. Yields of the second addition of DMAD to form 10 are typically modest: see Ref. 8d
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J. Am. Chem. Soc.
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Smith, C.D.1
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79
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77957765325
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Mitsudo, in Ref. 8d, reported <10% yield of 10 using the twin addition approach from norbornadiene
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Mitsudo, in Ref. 8d, reported <10% yield of 10 using the twin addition approach from norbornadiene.
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80
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77957803967
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The reaction was trialled using diphenylacetylene as the alkyne partner, however, only a trace of the desired product was detected in the crude reaction mixture
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The reaction was trialled using diphenylacetylene as the alkyne partner, however, only a trace of the desired product was detected in the crude reaction mixture.
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