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Volumn 581, Issue 1-2, 1999, Pages 170-175

The synthesis of a carborane gadolinium-DTPA complex for boron neutron capture therapy

Author keywords

Boron neutron capture therapy; Carborane; Chelating reagent; Gadolinium

Indexed keywords


EID: 0000305453     PISSN: 0022328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-328X(99)00049-2     Document Type: Article
Times cited : (27)

References (29)
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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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    • 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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    • 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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    • 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.
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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    Yamamoto, Y.3
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    • 0028286897 scopus 로고
    • 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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    • 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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    • 0000425082 scopus 로고    scopus 로고
    • 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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    • 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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    • Nakamura, H.1    Aoyagi, K.2    Yamamoto, Y.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.