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3
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McDowell, L.M.1
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4
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0030939030
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H. Duewel, E. Daub, V. Robinson and J. F. Honek, Biochemistry, ibid., 1997, 36, 3404;
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Duewel, H.1
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5
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I. Ojima, S. D. Kuduk, S. Chakravarty, M. Ourevitch and J. P. Begue, J. Am. Chem. Soc., 1997, 119, 5519;
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Ojima, I.1
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8
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0001212916
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Du Vigneaud, V.1
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10
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0001396301
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M. J. Brown, P. D. Milano, D. C. Lever, W. W. Epstein and D. C. Poulter, J. Am. Chem. Soc., 1991, 113, 3176;
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Brown, M.J.1
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0001255504
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C. C. Yang, C. K. Marlowe and R. Kania, J. Am. Chem. Soc., ibid., 1991, 113, 3177.
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Yang, C.C.1
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33845554149
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J. Fouropulos, Jr., and D. D. DesMarteau, J. Am. Chem. Soc., 1982, 104, 4260.
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Fouropulos Jr., J.1
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0011170266
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I. A. Koppel, R. W. Taft, F. Anvia, S.-Z. Zhu, L.-Q. Hu, K. Sung, D. D. DesMarteau, L. M. Yagupolski, Y. L. Yagupolski, N. V. Ignatev, N. V. Kondratenko, A. Y. Volkonskii, V. M. Vlasov, R. Notario and P. C. Maria, J. Am. Chem. Soc., 1994, 116, 3047.
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Kondratenko, N.V.11
Volkonskii, A.Y.12
Vlasov, V.M.13
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15
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Ying, W.1
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17
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33947457518
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From the reaction of 3 with aniline (2 equiv.) in boiling water, diphenylamine was isolated in 30% yield. Only trace amounts are obtained under the same conditions with diphenyliodonium bromide: F. M. Beringer, A. Brierley, M. Drexler, E. M. Gindler and C. C. Lumpkin, J. Am. Chem. Soc., 1953, 75, 2708.
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Beringer, F.M.1
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Drexler, M.3
Gindler, E.M.4
Lumpkin, C.C.5
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18
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0000589494
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and refs. therein
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L. A. Carpino, M. Beyermann, H. Wenschuh and M. Bienert, Acc. Chem. Res., 1996, 29, 268, and refs. therein.
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Carpino, L.A.1
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Wenschuh, H.3
Bienert, M.4
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19
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21844458265
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note
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3) -70.83, -70.86].
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20
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0032482050
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K. Severin, R. Bergs and W. Beck, Angew. Chem., Int. Ed., 1998, 37, 1086.
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Angew. Chem., Int. Ed.
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Severin, K.1
Bergs, R.2
Beck, W.3
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21
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21844472852
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manuscript in preparation
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4Ph was 70%, representing more than 80% per alkylation step: D. D. DesMarteau, J. Sayers and V. Montanari, manuscript in preparation.
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DesMarteau, D.D.1
Sayers, J.2
Montanari, V.3
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