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[摘要]:Suzuki-Miyaura reactions of 2-bromo-1-(trifluoromethanesulfonyloxy) naphthalene, readily available from 1-tetralone in two steps, afforded a variety of 1,2-diarylnaphthalenes. The reactions proceed with excellent chemoselectivity in favor of the bromide position, while the triflate remained unattacked. |
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