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note
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For examples of the preparation of 2-bromo-4-allylphenol, see: WO 2006107451. For related example of the preparation of 2-bromo-4-allylanisole, see Ref. 3.
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4644298316
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Although 2-allyl-4-bromoanisole 7 is known, it was prepared by allylation of commerciallyl available 4-bromophenol (97%), Claisen rearrangement (84%), and methylation (94%). For allylation and rearrangement, see
-
Although 2-allyl-4-bromoanisole 7 is known, it was prepared by allylation of commerciallyl available 4-bromophenol (97%), Claisen rearrangement (84%), and methylation (94%). For allylation and rearrangement, see: Bujok, R.; Bieniek, M.; Masnyk, M.; Michrowska, A.; Sarosiek, A.; Stȩpowska, H.; Arlt, D.; Grela, K. J. Org. Chem. 2004, 69, 6894-6896.
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26
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33751155775
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For the preparation of potassium aryltrifluoroborate, see
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For the preparation of potassium aryltrifluoroborate, see: Vedejs, E.; Chapman, R. W.; Fields, S. C.; Lin, S.; Schrimpf, M. R. J. Org. Chem. 1995, 60, 3020-3027.
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27
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0035813437
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For examples of the SuzukieMiyura reaction in the presence of the unprotected phenol, see
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For examples of the SuzukieMiyura reaction in the presence of the unprotected phenol, see: (a) Zhuravel, M. A.; Nguyen, S. T. Tetrahedron Lett. 2001, 42, 7925-7928;
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Zhuravel, M.A.1
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