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Barton, D. H. R.; Finet, J.-P; Giannotti, C.; Halley, F. J. Chem., Soc., Perkin Trans. 1, 1987, 241.
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Patel, B. A.; Ziegler, C. B.; Cortese, N. A.; Plevyak, J. E.; Zebovitz, T. C.; Terpko, M.; Heck, R. F. J. Org. Chem. 1978, 43, 2941.
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Heck, R.F.7
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Recent examples
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Recent examples: Iihama, X; Fu, J.-M.; Bourguignon, M.; Snieckus, V. Synthesis 1989, 184.
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Iihama, X.1
Fu, J.-M.2
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Snieckus, V.4
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Negishi, E. I.; Takahashi, T.; King, A. O. Org. Synth. 1988, 66, 67.
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Negishi, E.I.1
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King, A.O.3
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15
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0001295854
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Double arylations cannot be performed according to Scheme A, because aryl-di-Grignard compounds are not stable
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Double arylations cannot be performed according to Scheme A, because aryl-di-Grignard compounds are not stable: Bickelhaupt, F. Angew. Chem. 1987, 99, 1020;
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Bickelhaupt, F.1
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0007834995
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The free hydroxy group is essential to achieve regiospecific ortho-bromination
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The free hydroxy group is essential to achieve regiospecific ortho-bromination. Schmitz, E.; Pagenkopf, I. J. Prakt. Chem. 1985, 327, 998.
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Pagenkopf, I.2
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75749114356
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Alternative methods for ortho-bromination of phenols: Huston, R. C.; Ballard, M. M. Org. Synth. Coll. Vol. II, J. Wiley, London, 1943, p. 97.
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Org. Synth. Coll.
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Huston, R.C.1
Ballard, M.M.2
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Pearson, D. E.; Wysong, R. D.; Breder, C. V. J. Org. Chem. 1967, 32, 2358.
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Pearson, D.E.1
Wysong, R.D.2
Breder, C.V.3
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85081279834
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4Pd
-
4Pd.
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23
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85081213073
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4:26.00; 1-bromo-4-fluorobenzene: 0.02; 4-fluoro-l-iodobenzene: 0.70
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4:26.00; 1-bromo-4-fluorobenzene: 0.02; 4-fluoro-l-iodobenzene: 0.70.
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24
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85083010444
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Review concerning the synthesis of iodoarenes
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Review concerning the synthesis of iodoarenes: Merkushev, E. B. Synthesis 1988, 923.
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Reviews thiocyanation
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Reviews thiocyanation: Wood, J. L. Org. React. 1946, 3, 240-266.
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Org. React.
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Wood, J.L.1
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0004083142
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Patai S. ed., Wiley, London
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Gay, R. G., in: The Chemistry of Cyanates and Their Thio Derivatives, Pt. 2, Patai S. (ed.), Wiley, London, 1977, p. 819.
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The Chemistry of Cyanates and Their Thio Derivatives
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Gay, R.G.1
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85081222879
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Commercially available from Aldrich
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Commercially available from Aldrich.
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29
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Pearson, D. E.; Cowan, D.; Beckler, J. D. J. Org. Chem. 1959, 24, 504.
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