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Gebelein, C. G.; Frederick, G. D. J. Org. Chem. 1972, 37, 2211. Buckles, R. E.; Miller, J. L.; Thurmaier, R. J. J. Org. Chem. 1967, 32, 888. Sergeev, G. B.; Serguchev, Y. A.; Smirnov, V. V. Russ. Chem. Rev. (Engl. Transl.) 1973, 42, 697.
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Gebelein, C. G.; Frederick, G. D. J. Org. Chem. 1972, 37, 2211. Buckles, R. E.; Miller, J. L.; Thurmaier, R. J. J. Org. Chem. 1967, 32, 888. Sergeev, G. B.; Serguchev, Y. A.; Smirnov, V. V. Russ. Chem. Rev. (Engl. Transl.) 1973, 42, 697.
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(a) Byrnell, C. J. A.; Coombes, R. G.; Hart, L. S.; Whiting, M. C. J. Chem. Soc., Perkin Trans. 2 1983, 1079.
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19
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85088003079
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note
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4 is the most common solvent used in Organic Syntheses brominations.
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20
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4243465984
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Hanna, J. G.; Siggia, S. Anal. Chem. 1965, 37, 690. Garnier, F.; Dubois, J.-E. Bull. Soc. Chem. Fr. 1968, 3797.
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Hanna, J.G.1
Siggia, S.2
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21
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0003396538
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Hanna, J. G.; Siggia, S. Anal. Chem. 1965, 37, 690. Garnier, F.; Dubois, J.-E. Bull. Soc. Chem. Fr. 1968, 3797.
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Garnier, F.1
Dubois, J.-E.2
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22
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0000426238
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See: Ruasse, M.-F.; Dubois, J.-E. J. Am. Chem. Soc. 1975, 97, 1977. Olah, G. A.; Hockswender, T. R., Jr. J. Am. Chem. Soc. 1974, 96, 3574.
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Ruasse, M.-F.1
Dubois, J.-E.2
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23
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0042066178
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See: Ruasse, M.-F.; Dubois, J.-E. J. Am. Chem. Soc. 1975, 97, 1977. Olah, G. A.; Hockswender, T. R., Jr. J. Am. Chem. Soc. 1974, 96, 3574.
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Olah, G.A.1
Hockswender T.R., Jr.2
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24
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0347799216
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For previous studies of substrate deuterium KIEs for brominations, see refs 3b, 4, and also: (a) Denney, D. B.; Tunkel, N. Chem. Ind. 1959, 1383.
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Chem. Ind.
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Denney, D.B.1
Tunkel, N.2
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25
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0032540665
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(b) Koerner, T.; Brown, R. S.; Gainsforth, J. L.; Klobukowski, M. J. Am. Chem. Soc. 1998, 120, 5628.
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Koerner, T.1
Brown, R.S.2
Gainsforth, J.L.3
Klobukowski, M.4
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26
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0001463080
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(c) Bellucci, G.; Chiappe, C.; Lo Moro, G. J. Org. Chem. 1997, 62, 3176.
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Bellucci, G.1
Chiappe, C.2
Lo Moro, G.3
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28
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0000417411
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(e) Slebocka-Tilk, H.; Motallebi, S.; Nagorski, R. W.; Turner, P.; Brown, R. S.; McDonald, R. J. Am. Chem. Soc. 1995, 117, 8769.
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Slebocka-Tilk, H.1
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Turner, P.4
Brown, R.S.5
McDonald, R.6
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29
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0032565094
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(f) Slebocka-Tilk, H.; Neverov, A.; Motallebi, S.; Brown, R. S.; Donini, O.; Gainsforth, J. L.; Klobukoski, M. J. Am. Chem. Soc. 1998, 120, 2578.
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Slebocka-Tilk, H.1
Neverov, A.2
Motallebi, S.3
Brown, R.S.4
Donini, O.5
Gainsforth, J.L.6
Klobukoski, M.7
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30
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0042075540
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The only previous measurement of carbon KIEs from bromination gave results within experimental error of unity: Ropp, G. A.; Raaen, V. F.; Weinbergur, A. J. J. Am. Chem. Soc. 1953, 75, 3694.
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J. Am. Chem. Soc.
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Ropp, G.A.1
Raaen, V.F.2
Weinbergur, A.J.3
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32
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85088001222
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note
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2] was judged visually by comparison with standard solutions.
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35
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0024841752
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The calculations used the program QUIVER (Saunders: M.; Laidig, K. E.; Wolfsberg, M. J. Am. Chem. Soc. 1989, 111, 8989) with Becke3LYP frequencies scaled by 0.9614. ( Scott, A. P.; Radom, L. J. Phys. Chem. 1996, 100, 16502.)
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(1989)
J. Am. Chem. Soc.
, vol.111
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Saunders, M.1
Laidig, K.E.2
Wolfsberg, M.3
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36
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0011083273
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The calculations used the program QUIVER (Saunders: M.; Laidig, K. E.; Wolfsberg, M. J. Am. Chem. Soc. 1989, 111, 8989) with Becke3LYP frequencies scaled by 0.9614. ( Scott, A. P.; Radom, L. J. Phys. Chem. 1996, 100, 16502.)
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(1996)
J. Phys. Chem.
, vol.100
, pp. 16502
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Scott, A.P.1
Radom, L.2
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