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85030189584
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0025219972
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26
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85025772558
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The monolithiation and silylation were carried out at -110°C, see: Chen, L. S.; Chen, G. J. J. Organomet. Chem. 1980, 193, 283.
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27
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85030192762
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note
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In the reaction of the corresponding alcohol with HCl(g) and trioxane to yield linker 4, substantial amount of protiodesilylation (@50%) took place.
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28
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85030194473
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note
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2 afforded the same product in quantitative yield. P-4, however, reacted smoothly to afford 67% yield of the desired product (p-bromoanisole)
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31
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Some of the corresponding benzylic chloride was also observed. See also: Takahashi, M.; Hatano K.; Kimura, M.; Watanabe, T.; Oriyama, T.; Koga, K. Tetrahedron Lett. 1994, 35, 579.
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Oriyama, T.5
Koga, K.6
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