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1
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0028129338
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Recent examples: (a) Lanthanide-cyclodextrin complex; T.J. Wenzel, M.S. Bogyo, E.L. Lebeau, J. Am. Chem. Soc. 116 (1994) 4858. (b) Gadolinium complexes: P.F. Sieving, A.D. Watson, S.M. Rocklage, Bioconjugate Chem. 1 (1990) 65. (c) Terbium complex: M.P. Bailey, B.F. Rocks, C. Riley, Analyst 109 (1984) 1449. (d) Indium complexes: C.H. Paik, V.K. Sood, N. Le, J.A. Carrasquillo, J.C. Reynolds, R.D. Neumann, R.C. Rega, Nucl. Med. Biol. 19 (1992) 517. (e) Technetium complexes: Y. B. J. Aldenhoff, M. J. P. G. van Kroonenburg, S. V. M. Zimmy, P. P. C. A. Menheere, L. H. Koole, J. Chem. Soc. Chem. Commun. (1995) 523.
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Wenzel, T.J.1
Bogyo, M.S.2
Lebeau, E.L.3
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2
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0025200083
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Recent examples: (a) Lanthanide-cyclodextrin complex; T.J. Wenzel, M.S. Bogyo, E.L. Lebeau, J. Am. Chem. Soc. 116 (1994) 4858. (b) Gadolinium complexes: P.F. Sieving, A.D. Watson, S.M. Rocklage, Bioconjugate Chem. 1 (1990) 65. (c) Terbium complex: M.P. Bailey, B.F. Rocks, C. Riley, Analyst 109 (1984) 1449. (d) Indium complexes: C.H. Paik, V.K. Sood, N. Le, J.A. Carrasquillo, J.C. Reynolds, R.D. Neumann, R.C. Rega, Nucl. Med. Biol. 19 (1992) 517. (e) Technetium complexes: Y. B. J. Aldenhoff, M. J. P. G. van Kroonenburg, S. V. M. Zimmy, P. P. C. A. Menheere, L. H. Koole, J. Chem. Soc. Chem. Commun. (1995) 523.
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Sieving, P.F.1
Watson, A.D.2
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3
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0021683694
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Recent examples: (a) Lanthanide-cyclodextrin complex; T.J. Wenzel, M.S. Bogyo, E.L. Lebeau, J. Am. Chem. Soc. 116 (1994) 4858. (b) Gadolinium complexes: P.F. Sieving, A.D. Watson, S.M. Rocklage, Bioconjugate Chem. 1 (1990) 65. (c) Terbium complex: M.P. Bailey, B.F. Rocks, C. Riley, Analyst 109 (1984) 1449. (d) Indium complexes: C.H. Paik, V.K. Sood, N. Le, J.A. Carrasquillo, J.C. Reynolds, R.D. Neumann, R.C. Rega, Nucl. Med. Biol. 19 (1992) 517. (e) Technetium complexes: Y. B. J. Aldenhoff, M. J. P. G. van Kroonenburg, S. V. M. Zimmy, P. P. C. A. Menheere, L. H. Koole, J. Chem. Soc. Chem. Commun. (1995) 523.
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Bailey, M.P.1
Rocks, B.F.2
Riley, C.3
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4
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44049117926
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Recent examples: (a) Lanthanide-cyclodextrin complex; T.J. Wenzel, M.S. Bogyo, E.L. Lebeau, J. Am. Chem. Soc. 116 (1994) 4858. (b) Gadolinium complexes: P.F. Sieving, A.D. Watson, S.M. Rocklage, Bioconjugate Chem. 1 (1990) 65. (c) Terbium complex: M.P. Bailey, B.F. Rocks, C. Riley, Analyst 109 (1984) 1449. (d) Indium complexes: C.H. Paik, V.K. Sood, N. Le, J.A. Carrasquillo, J.C. Reynolds, R.D. Neumann, R.C. Rega, Nucl. Med. Biol. 19 (1992) 517. (e) Technetium complexes: Y. B. J. Aldenhoff, M. J. P. G. van Kroonenburg, S. V. M. Zimmy, P. P. C. A. Menheere, L. H. Koole, J. Chem. Soc. Chem. Commun. (1995) 523.
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Paik, C.H.1
Sood, V.K.2
Le, N.3
Carrasquillo, J.A.4
Reynolds, J.C.5
Neumann, R.D.6
Rega, R.C.7
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5
-
-
0028958879
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Recent examples: (a) Lanthanide-cyclodextrin complex; T.J. Wenzel, M.S. Bogyo, E.L. Lebeau, J. Am. Chem. Soc. 116 (1994) 4858. (b) Gadolinium complexes: P.F. Sieving, A.D. Watson, S.M. Rocklage, Bioconjugate Chem. 1 (1990) 65. (c) Terbium complex: M.P. Bailey, B.F. Rocks, C. Riley, Analyst 109 (1984) 1449. (d) Indium complexes: C.H. Paik, V.K. Sood, N. Le, J.A. Carrasquillo, J.C. Reynolds, R.D. Neumann, R.C. Rega, Nucl. Med. Biol. 19 (1992) 517. (e) Technetium complexes: Y. B. J. Aldenhoff, M. J. P. G. van Kroonenburg, S. V. M. Zimmy, P. P. C. A. Menheere, L. H. Koole, J. Chem. Soc. Chem. Commun. (1995) 523.
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(1995)
J. Chem. Soc. Chem. Commun.
, pp. 523
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Aldenhoff, Y.B.J.1
Van Kroonenburg, M.J.P.G.2
Zimmy, S.V.M.3
Menheere, P.P.C.A.4
Koole, L.H.5
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7
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8
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11
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Review Papers: (a) Y. Yamamoto, Pure. Appl. Chem. 63 (1991) 423. (b) M. F. Hawthorne, Angew. Chem. Int. Ed. Engl. 32 (1993) 950. (c) R. F. Barth, A. H. Soloway, R. G. Fairchild, Cancer Research 50 (1990) 1061. (d) A. H. Soloway, W. Tjarks, B. A. Barnum, F.-G. Rong, R. F. Barth, I. M. Wyzlic, J. G. Wilson, Chem. Rev. 98 (1998) 1515.
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Review Papers: (a) Y. Yamamoto, Pure. Appl. Chem. 63 (1991) 423. (b) M. F. Hawthorne, Angew. Chem. Int. Ed. Engl. 32 (1993) 950. (c) R. F. Barth, A. H. Soloway, R. G. Fairchild, Cancer Research 50 (1990) 1061. (d) A. H. Soloway, W. Tjarks, B. A. Barnum, F.-G. Rong, R. F. Barth, I. M. Wyzlic, J. G. Wilson, Chem. Rev. 98 (1998) 1515.
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Barth, R.F.1
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Review Papers: (a) Y. Yamamoto, Pure. Appl. Chem. 63 (1991) 423. (b) M. F. Hawthorne, Angew. Chem. Int. Ed. Engl. 32 (1993) 950. (c) R. F. Barth, A. H. Soloway, R. G. Fairchild, Cancer Research 50 (1990) 1061. (d) A. H. Soloway, W. Tjarks, B. A. Barnum, F.-G. Rong, R. F. Barth, I. M. Wyzlic, J. G. Wilson, Chem. Rev. 98 (1998) 1515.
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Soloway, A.H.1
Tjarks, W.2
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Barth, R.F.5
Wyzlic, I.M.6
Wilson, J.G.7
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G. W. Kabalka, G. T. Smith, J. P. Dyke, W. S. Reid, C. P. D. Longford, T. G. Roberts, N. K. Reddy, E. Buonocore, K. F. Hübner, J. Nucl. Med. 38 (1997) 1762.
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18
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B. Larsson, J. Crawford, R. Weinreich (Eds.), Plenum Press, New York
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Y. Yamamoto, J. Cai, H. Nemoto, H. Nakamura, F. Girard, K. Yoshida, H. Fukuda, in: B. Larsson, J. Crawford, R. Weinreich (Eds.), Advances in Neutron Capture Therapy, Plenum Press, New York, 1997, p. 436.
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Yamamoto, Y.1
Cai, J.2
Nemoto, H.3
Nakamura, H.4
Girard, F.5
Yoshida, K.6
Fukuda, H.7
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19
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0347357529
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-
note
-
In the case of using NaHMDS instead of KHMDS, the yield of 8 was increased. The structure of 8 was not clear, because the position, to which the second ester group attached, could not be determined.
-
-
-
-
20
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33845379388
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J. Tsuji, I. Shimizu, I. Mikami, Y. Ohashi, T. Sugiura, K. Takahashi, J. Org. Chem. 50 (1985) 1523.
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Sugiura, T.5
Takahashi, K.6
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21
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0005731297
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This choice of the catalyst combination gives often better results as reported in our recent papers; H. Nemoto, F.-G. Rong, Y. Yamamoto, J. Org. Chem. 55 (1990) 6065. H. Nemoto, J. Cai, Y. Yamamoto, J. Chem. Soc. Chem. Commun. (1994) 577.
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Nemoto, H.1
Rong, F.-G.2
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22
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0028286897
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This choice of the catalyst combination gives often better results as reported in our recent papers; H. Nemoto, F.-G. Rong, Y. Yamamoto, J. Org. Chem. 55 (1990) 6065. H. Nemoto, J. Cai, Y. Yamamoto, J. Chem. Soc. Chem. Commun. (1994) 577.
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A. D. Whittaker, D. P. Kelly, M. Pardee, R. F. Martin, in: B. J. Allen, D. E. Moore, B. V. Harrington (Eds), Progress in Neutron Capture Therapy for Cancer; Plenum Press, New York, 1992, p. 231.
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(a) F. Girard, H. Nakamura, H. Fukuda, Y. Yamamoto, K, Yoshida, in: Y. Ishii et al. (Eds.), Recent Advances in Biomedical Imaging, Elsevier Science, Amsterdam, 1997, p. 201.
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Girard, F.1
Nakamura, H.2
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0346727037
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B. Larsson, J. Crawford, R. Weinreich (Eds.), Plenum Press, New York
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(b) F. Girard, H. Fukuda, H. Nakamura, Y. Yamamoto, K. Yoshida, in B. Larsson, J. Crawford, R. Weinreich (Eds.), Advances in Neutron Capture Therapy, Plenum Press, New York, 1997, p. 271.
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Fukuda, H.2
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Yoshida, K.5
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26
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0030353396
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-
Diluted condition was important for preparing monosubstituted carboranes; see J. Cai, H. Nemoto, H. Nakamura, B. Singaram, Y. Yamamoto, Chem. Lett. (1996) 791. H. Nakamura, K. Aoyagi, Y. Yamamoto, J. Org. Chem. 62 (1997) 780. H. Nakamura, K. Aoyagi, Y. Yamamoto, J. Am. Chem. Soc. 120 (1998) 1167.
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Chem. Lett.
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27
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0000425082
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-
Diluted condition was important for preparing monosubstituted carboranes; see J. Cai, H. Nemoto, H. Nakamura, B. Singaram, Y. Yamamoto, Chem. Lett. (1996) 791. H. Nakamura, K. Aoyagi, Y. Yamamoto, J. Org. Chem. 62 (1997) 780. H. Nakamura, K. Aoyagi, Y. Yamamoto, J. Am. Chem. Soc. 120 (1998) 1167.
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28
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0032542570
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Diluted condition was important for preparing monosubstituted carboranes; see J. Cai, H. Nemoto, H. Nakamura, B. Singaram, Y. Yamamoto, Chem. Lett. (1996) 791. H. Nakamura, K. Aoyagi, Y. Yamamoto, J. Org. Chem. 62 (1997) 780. H. Nakamura, K. Aoyagi, Y. Yamamoto, J. Am. Chem. Soc. 120 (1998) 1167.
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