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Volumn 16, Issue 2, 2005, Pages 255-264

Design and synthesis of functionalized cyclopentadienyl tricarbonylmetal complexes for technetium-94m PET imaging of estrogen receptors

Author keywords

[No Author keywords available]

Indexed keywords

CHELATION; MEDICAL IMAGING; RHENIUM; RHENIUM COMPOUNDS; SYNTHESIS (CHEMICAL); TECHNETIUM; TECHNETIUM COMPOUNDS; TUMORS;

EID: 15244361767     PISSN: 10431802     EISSN: None     Source Type: Journal    
DOI: 10.1021/bc049770g     Document Type: Article
Times cited : (38)

References (59)
  • 3
    • 0031851686 scopus 로고    scopus 로고
    • Methyl hypofluorite in the synthesis of 16-methoxyestradiol stereoisomers
    • Jonson, S. D., d'Avignon, D. A., Katzenellenbogen, J. A., and Welch, M. J. (1998) Methyl hypofluorite in the synthesis of 16-methoxyestradiol stereoisomers. Steroids 63, 470-478.
    • (1998) Steroids , vol.63 , pp. 470-478
    • Jonson, S.D.1    D'Avignon, D.A.2    Katzenellenbogen, J.A.3    Welch, M.J.4
  • 6
    • 0036006421 scopus 로고    scopus 로고
    • Synthesis of 2, 16α- and 4, 16α-difluoroestradiols and their 11β-methoxy derivatives as potential estrogen receptor-binding radiopharmaceuticals
    • Seimbille, Y., Ali, H., and Van Lier, J. E. (2002) Synthesis of 2, 16α- and 4, 16α-difluoroestradiols and their 11β-methoxy derivatives as potential estrogen receptor-binding radiopharmaceuticals. J. Am. Chem. Soc., Perkin Trans. 1 657-663.
    • (2002) J. Am. Chem. Soc., Perkin Trans. , vol.1 , pp. 657-663
    • Seimbille, Y.1    Ali, H.2    Van Lier, J.E.3
  • 8
    • 0030152907 scopus 로고    scopus 로고
    • Carbon-11-labeled estrogens as potential imaging agents for breast tumors
    • Dence, C. S., Napolitano, E., Katzenellenbogen, J. A., and Welch, M. J. (1996) Carbon-11-labeled estrogens as potential imaging agents for breast tumors. Nucl. Med. Biol. 23, 491-496.
    • (1996) Nucl. Med. Biol. , vol.23 , pp. 491-496
    • Dence, C.S.1    Napolitano, E.2    Katzenellenbogen, J.A.3    Welch, M.J.4
  • 9
    • 0027389803 scopus 로고
    • Synthesis, radiolabeling and tissue distribution of 11β-fluoroalkyl- and 11β-fluoroalkoxy-substituted estrogens: Target tissue uptake selectivity and defluorination of a homologous series of fluorine-18-labeled estrogens
    • French, A. N., Napolitano, E., Vanbrocklin, H. F., Hanson, R. N., Welch, M. J., and Katzenellenbogen, J. A. (1993) Synthesis, radiolabeling and tissue distribution of 11β-fluoroalkyl- and 11β-fluoroalkoxy-substituted estrogens: target tissue uptake selectivity and defluorination of a homologous series of fluorine-18-labeled estrogens. Nucl. Med. Biol. 20, 31-47.
    • (1993) Nucl. Med. Biol. , vol.20 , pp. 31-47
    • French, A.N.1    Napolitano, E.2    Vanbrocklin, H.F.3    Hanson, R.N.4    Welch, M.J.5    Katzenellenbogen, J.A.6
  • 10
    • 0025251173 scopus 로고
    • 11β-Methoxy-, 11β-ethyl, and 17α-ethynyl-substituted 16α-fluoroestradiols: Receptor-based imaging agents with enhanced uptake efficiency and selectivity
    • Pomper, M. G., VanBrocklin, H., Thieme, A. M., Thomas, R. D., Kiesewetter, D. O., Carlson, K. E., Mathias, C. J., Welch, M. J., and Katzenellenbogen, J. A. (1990) 11β-Methoxy-, 11β-ethyl, and 17α-ethynyl-substituted 16α-fluoroestradiols: receptor-based imaging agents with enhanced uptake efficiency and selectivity. J. Med. Chem. 33, 3143-3155.
    • (1990) J. Med. Chem. , vol.33 , pp. 3143-3155
    • Pomper, M.G.1    VanBrocklin, H.2    Thieme, A.M.3    Thomas, R.D.4    Kiesewetter, D.O.5    Carlson, K.E.6    Mathias, C.J.7    Welch, M.J.8    Katzenellenbogen, J.A.9
  • 11
    • 0021751581 scopus 로고
    • Preparation of four fluorine-18-labeled estrogens and their selective uptakes in target tissues of immature rats
    • Kiesewetter, D. O., Kilbourn, M. R., Landvatter, S. W., Heiman, D. F., Katzenellenbogen, J. A., and Welch, M. J. (1984) Preparation of four fluorine-18-labeled estrogens and their selective uptakes in target tissues of immature rats. J. Nucl. Med. 25, 1212-1221.
    • (1984) J. Nucl. Med. , vol.25 , pp. 1212-1221
    • Kiesewetter, D.O.1    Kilbourn, M.R.2    Landvatter, S.W.3    Heiman, D.F.4    Katzenellenbogen, J.A.5    Welch, M.J.6
  • 12
    • 44049124825 scopus 로고
    • Preparation and evaluation of 17-ethynyl-substituted 16α-[18F] fluoroestradiols: Selective receptor-based PET imaging agents
    • Vanbrocklin, H. F., Pomper, M. G., Carlson, K. E., Welch, M. J., and Katzenellenbogen, J. A. (1992) Preparation and evaluation of 17-ethynyl-substituted 16α-[18F]fluoroestradiols: selective receptor-based PET imaging agents. Nucl. Med. Biol. 19, 363-374.
    • (1992) Nucl. Med. Biol. , vol.19 , pp. 363-374
    • Vanbrocklin, H.F.1    Pomper, M.G.2    Carlson, K.E.3    Welch, M.J.4    Katzenellenbogen, J.A.5
  • 14
    • 0033024916 scopus 로고    scopus 로고
    • Positron emission tomographic assessment of "metabolic flare" to predict response of metastatic breast cancer to antiestrogen therapy
    • Dehdashti, F., Flanagan, F. L., Mortimer, J. E., Katzenellenbogen, J. A., Welch, M. J., and Siegel, B. A. (1999) Positron emission tomographic assessment of "metabolic flare" to predict response of metastatic breast cancer to antiestrogen therapy. Eur. J. Nucl. Med. 26, 51-56.
    • (1999) Eur. J. Nucl. Med. , vol.26 , pp. 51-56
    • Dehdashti, F.1    Flanagan, F.L.2    Mortimer, J.E.3    Katzenellenbogen, J.A.4    Welch, M.J.5    Siegel, B.A.6
  • 15
    • 0032342440 scopus 로고    scopus 로고
    • The biomedical chemistry of technetium and rhenium
    • Dilworth, J. R., and Parrott, S. J. (1998) The biomedical chemistry of technetium and rhenium. Chem. Soc. Rev. 27, 43-55.
    • (1998) Chem. Soc. Rev. , vol.27 , pp. 43-55
    • Dilworth, J.R.1    Parrott, S.J.2
  • 16
    • 0001201879 scopus 로고    scopus 로고
    • High- and low-valency organometallic compounds of technetium and rhenium
    • Alberto, R. (1996) High- and low-valency organometallic compounds of technetium and rhenium. Top. Curr. Chem. 176, 149-187.
    • (1996) Top. Curr. Chem. , vol.176 , pp. 149-187
    • Alberto, R.1
  • 17
    • 33748216792 scopus 로고
    • Technetium radiopharmaceuticals - Fundamentals, synthesis, structure, and development
    • Schwochau, K. (1994) Technetium radiopharmaceuticals - fundamentals, synthesis, structure, and development. Angew. Chem., Int. Ed. Engl. 33, 2258-2267.
    • (1994) Angew. Chem., Int. Ed. Engl. , vol.33 , pp. 2258-2267
    • Schwochau, K.1
  • 18
    • 0027389181 scopus 로고
    • Rhenium-186-labeled monoclonal antibodies for radioimmunotherapy: Preparation and evaluation
    • John, E., Thakur, M. L., DeFulvio, J., McDevitt, M. R., and Damjanov, I. (1993) Rhenium-186-labeled monoclonal antibodies for radioimmunotherapy: preparation and evaluation. J. Nucl. Med. 34, 260-267.
    • (1993) J. Nucl. Med. , vol.34 , pp. 260-267
    • John, E.1    Thakur, M.L.2    DeFulvio, J.3    McDevitt, M.R.4    Damjanov, I.5
  • 19
    • 0027455792 scopus 로고
    • Synthesis of carrier-free rhenium-188(V)DMSA using triphenylphosphine as a facile reducing agent
    • Lisic, E. C., Mirzadeh, S., and Knapp, F. F., Jr. (1993) Synthesis of carrier-free rhenium-188(V)DMSA using triphenylphosphine as a facile reducing agent. J. Labelled Compd. Radiopharm. 33, 65-75.
    • (1993) J. Labelled Compd. Radiopharm. , vol.33 , pp. 65-75
    • Lisic, E.C.1    Mirzadeh, S.2    Knapp Jr., F.F.3
  • 20
    • 0242266521 scopus 로고    scopus 로고
    • 7α- and 17α-Substituted estrogens containing tridentate tricarbonyl rhenium/technetium complexes: Synthesis of estrogen receptor imaging agents and evaluation using microPET with technetium-94m
    • Luyt, L. G., Bigott, H. M., Welch, M. J., and Katzenellenbogen, J. A. (2003) 7α- and 17α-Substituted estrogens containing tridentate tricarbonyl rhenium/technetium complexes: synthesis of estrogen receptor imaging agents and evaluation using microPET with technetium-94m. Bioorg. Med. Chem. 11, 4977-4989.
    • (2003) Bioorg. Med. Chem. , vol.11 , pp. 4977-4989
    • Luyt, L.G.1    Bigott, H.M.2    Welch, M.J.3    Katzenellenbogen, J.A.4
  • 21
    • 0032893425 scopus 로고    scopus 로고
    • Integrated "3+1" oxorhenium(V) complexes as estrogen mimics
    • Skaddan, M. B., and Katzenellenbogen, J. A. (1999) Integrated "3+1" oxorhenium(V) complexes as estrogen mimics. Bioconjugate Chem. 10, 119-129.
    • (1999) Bioconjugate Chem. , vol.10 , pp. 119-129
    • Skaddan, M.B.1    Katzenellenbogen, J.A.2
  • 22
    • 0028218557 scopus 로고
    • Synthetic strategy for organometallic complexes of rhenium with exceptionally high affinity for the estradiol receptor; their potential use as imaging and therapeutic agents
    • Top, S., Vessieres, A., and Jaouen, G. (1994) Synthetic strategy for organometallic complexes of rhenium with exceptionally high affinity for the estradiol receptor; their potential use as imaging and therapeutic agents. Chem. Commun. 453-454.
    • (1994) Chem. Commun. , pp. 453-454
    • Top, S.1    Vessieres, A.2    Jaouen, G.3
  • 23
    • 0032541990 scopus 로고    scopus 로고
    • Ligands for the estrogen receptor containing cyclopentadienyltricarbonylrhenium units
    • Spradau, T. W., and Katzenellenbogen, J. A. (1998) Ligands for the estrogen receptor containing cyclopentadienyltricarbonylrhenium units. Bioorg. Med. Chem. Lett. 8, 3235-3240.
    • (1998) Bioorg. Med. Chem. Lett. , vol.8 , pp. 3235-3240
    • Spradau, T.W.1    Katzenellenbogen, J.A.2
  • 25
    • 0345440144 scopus 로고    scopus 로고
    • Synthesis and binding affinities of novel Recontaining 7α-substituted estradiol complexes: Models for breast cancer imaging agents
    • Skaddan, M. B., Wuest, F. R., and Katzenellenbogen, J. A. (1999) Synthesis and binding affinities of novel Recontaining 7α-substituted estradiol complexes: models for breast cancer imaging agents. J. Org. Chem. 64, 8108-8121.
    • (1999) J. Org. Chem. , vol.64 , pp. 8108-8121
    • Skaddan, M.B.1    Wuest, F.R.2    Katzenellenbogen, J.A.3
  • 26
    • 0034681534 scopus 로고    scopus 로고
    • Solid-supported hydrazine substrate for labeling estradiol ligands with rhenium
    • Arterburn, J. B., Rao, K. V., and Perry, M. C. (2000) Solid-supported hydrazine substrate for labeling estradiol ligands with rhenium. Angew. Chem., Int. Ed. 39, 771-772.
    • (2000) Angew. Chem., Int. Ed. , vol.39 , pp. 771-772
    • Arterburn, J.B.1    Rao, K.V.2    Perry, M.C.3
  • 27
    • 0039710691 scopus 로고    scopus 로고
    • Synthesis and binding affinities of new 17α-substituted estradiol-rhenium "n+1" mixed-ligand and thioethercarbonyl complexes
    • Wust, F., Carlson, K. E., Katzenellenbogen, J. A., Spies, H., and Johannsen, B. (1998) Synthesis and binding affinities of new 17α-substituted estradiol-rhenium "n+1" mixed-ligand and thioethercarbonyl complexes. Steroids 63, 665-671.
    • (1998) Steroids , vol.63 , pp. 665-671
    • Wust, F.1    Carlson, K.E.2    Katzenellenbogen, J.A.3    Spies, H.4    Johannsen, B.5
  • 28
    • 0030593865 scopus 로고    scopus 로고
    • Synthesis of "3+1" mixed-ligand oxorhenium(V) complexes containing modified 3, 17β-estradiol
    • Wuest, F., Spies, H., and Johannsen, B. (1996) Synthesis of "3+1" mixed-ligand oxorhenium(V) complexes containing modified 3, 17β-estradiol. Bioorg. Med. Chem. Lett. 6, 2729-2734.
    • (1996) Bioorg. Med. Chem. Lett. , vol.6 , pp. 2729-2734
    • Wuest, F.1    Spies, H.2    Johannsen, B.3
  • 29
    • 1542706211 scopus 로고    scopus 로고
    • Synthesis of a tetradentate oxorhenium(V) complex mimic of a steroidal estrogen
    • Hom, R. K., and Katzenellenbogen, J. A. (1997) Synthesis of a tetradentate oxorhenium(V) complex mimic of a steroidal estrogen. J. Org. Chem. 62, 6290-6297.
    • (1997) J. Org. Chem. , vol.62 , pp. 6290-6297
    • Hom, R.K.1    Katzenellenbogen, J.A.2
  • 30
    • 0029145533 scopus 로고
    • Rhenium carbonyl complexes of β-estradiol derivatives with high affinity for the estradiol receptor: An approach to selective organometallic radiopharmaceuticals
    • Top, S., El Hafa, H., Vessieres, A., Quivy, J., Vaissermann, J., Hughes, D. W., McGlinchey, M. J., Mornon, J.-P., Thoreau, E., and Jaouen, G. (1995) Rhenium carbonyl complexes of β-estradiol derivatives with high affinity for the estradiol receptor: an approach to selective organometallic radiopharmaceuticals. J. Am. Chem. Soc. 117, 8372-8380.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 8372-8380
    • Top, S.1    El Hafa, H.2    Vessieres, A.3    Quivy, J.4    Vaissermann, J.5    Hughes, D.W.6    McGlinchey, M.J.7    Mornon, J.-P.8    Thoreau, E.9    Jaouen, G.10
  • 31
    • 0028025435 scopus 로고
    • Estradiol-derivatives. Synthesis, organ distribution and tumor affinity
    • Wenzel, M., and Klinger, C. (1994) Estradiol-derivatives. Synthesis, organ distribution and tumor affinity. J. Labelled Compd. Radiopharm. 34, 981-987.
    • (1994) J. Labelled Compd. Radiopharm. , vol.34 , pp. 981-987
    • Wenzel, M.1    Klinger, C.2
  • 32
    • 0036186145 scopus 로고    scopus 로고
    • Aryl cyclopentadienyl tricarbonyl rhenium complexes: Novel ligands for the estrogen receptor with potential use as estrogen radiopharmaceuticals
    • Mull, E. S., Sattigeri, V. J., Rodriguez, A. L., and Katzenellenbogen, J. A. (2002) Aryl cyclopentadienyl tricarbonyl rhenium complexes: novel ligands for the estrogen receptor with potential use as estrogen radiopharmaceuticals. Bioorg. Med. Chem. 10, 1381-1398.
    • (2002) Bioorg. Med. Chem. , vol.10 , pp. 1381-1398
    • Mull, E.S.1    Sattigeri, V.J.2    Rodriguez, A.L.3    Katzenellenbogen, J.A.4
  • 33
    • 0035925190 scopus 로고    scopus 로고
    • First anti-estrogen in the cyclopentadienyl rhenium tricarbonyl series. Synthesis and study of antiproliferative effects
    • Jaouen, G., Top, S., Vessieres, A., Pigeon, P., Leclercq, G., and Laios, I. (2001) First anti-estrogen in the cyclopentadienyl rhenium tricarbonyl series. Synthesis and study of antiproliferative effects. Chem. Commun. 383-384.
    • (2001) Chem. Commun. , pp. 383-384
    • Jaouen, G.1    Top, S.2    Vessieres, A.3    Pigeon, P.4    Leclercq, G.5    Laios, I.6
  • 34
    • 0033950583 scopus 로고    scopus 로고
    • A novel and mild metal-exchange reaction in the organometallic cyclopentadienyl series: 1, 1′-diaryl 2-cymantrenyl 1-butene as an example
    • Top, S., Kaloun, E. B., and Jaouen, G. (2000) A novel and mild metal-exchange reaction in the organometallic cyclopentadienyl series: 1, 1′-diaryl 2-cymantrenyl 1-butene as an example. J. Am. Chem. Soc. 122, 736-737.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 736-737
    • Top, S.1    Kaloun, E.B.2    Jaouen, G.3
  • 35
    • 0026655598 scopus 로고
    • Technetium-99m labeling of cymantrene analogs with various substituents. A new preparation of technetium-99m radiodiagnostics
    • Wenzel, M. (1992) Technetium-99m labeling of cymantrene analogs with various substituents. A new preparation of technetium-99m radiodiagnostics. J. Labelled Compd. Radiopharm. 31, 641-650.
    • (1992) J. Labelled Compd. Radiopharm. , vol.31 , pp. 641-650
    • Wenzel, M.1
  • 36
    • 0000056864 scopus 로고    scopus 로고
    • Preparation of cyclopentadienyltricarbonylrhenium complexes using a double ligand-transfer reaction
    • Spradau, T. W., and Katzenellenbogen, J. A. (1998) Preparation of cyclopentadienyltricarbonylrhenium complexes using a double ligand-transfer reaction. Organometallics 17, 2009-2017.
    • (1998) Organometallics , vol.17 , pp. 2009-2017
    • Spradau, T.W.1    Katzenellenbogen, J.A.2
  • 37
    • 0001400985 scopus 로고    scopus 로고
    • A convenient three-component synthesis of substituted cyclopentadienyl tricarbonyl rhenium complexes
    • Minutolo, F., and Katzenellenbogen, J. A. (1998) A convenient three-component synthesis of substituted cyclopentadienyl tricarbonyl rhenium complexes. J. Am. Chem. Soc. 120, 4514-4515.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 4514-4515
    • Minutolo, F.1    Katzenellenbogen, J.A.2
  • 38
    • 0032561810 scopus 로고    scopus 로고
    • Boronic acids in the three-component synthesis of carbon-substituted cyclopentadienyl tricarbonyl rhenium complexes
    • Minutolo, F., and Katzenellenbogen, J. A. (1998) Boronic acids in the three-component synthesis of carbon-substituted cyclopentadienyl tricarbonyl rhenium complexes. J. Am. Chem. Soc. 120, 13264-13265.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 13264-13265
    • Minutolo, F.1    Katzenellenbogen, J.A.2
  • 39
    • 0003100912 scopus 로고    scopus 로고
    • Synthesis of cyclopentadienyltricarbonylrhenium(I) carboxylic acid from perrhenate
    • Top, S., Lehn, J.-S., Morel, P., and Jaouen, G. (1999) Synthesis of cyclopentadienyltricarbonylrhenium(I) carboxylic acid from perrhenate. J. Organomet. Chem. 583, 63-68.
    • (1999) J. Organomet. Chem. , vol.583 , pp. 63-68
    • Top, S.1    Lehn, J.-S.2    Morel, P.3    Jaouen, G.4
  • 40
    • 0345358448 scopus 로고    scopus 로고
    • Exploration of the bicyclo[3.3.1]nonane system as a template for the development of new ligands for the estrogen receptor
    • Muthyala, R. S., Carlson, K. E., and Katzenellenbogen, J. A. (2003) Exploration of the bicyclo[3.3.1]nonane system as a template for the development of new ligands for the estrogen receptor. Bioorg. Med. Chem. Lett. 13, 4485-4488.
    • (2003) Bioorg. Med. Chem. Lett. , vol.13 , pp. 4485-4488
    • Muthyala, R.S.1    Carlson, K.E.2    Katzenellenbogen, J.A.3
  • 41
    • 0344670184 scopus 로고    scopus 로고
    • Bridged bicyclic cores containing a 1,1-diarylethylene motif are high-affinity subtype-selective ligands for the estrogen receptor
    • Muthyala, R. S., Sheng, S., Carlson, K. E., Katzenellenbogen, B. S., and Katzenellenbogen, J. A. (2003) Bridged bicyclic cores containing a 1,1-diarylethylene motif are high-affinity subtype-selective ligands for the estrogen receptor. J. Med. Chem. 46, 1589-1602.
    • (2003) J. Med. Chem. , vol.46 , pp. 1589-1602
    • Muthyala, R.S.1    Sheng, S.2    Carlson, K.E.3    Katzenellenbogen, B.S.4    Katzenellenbogen, J.A.5
  • 43
    • 0001756967 scopus 로고
    • 94mTc from enriched molybdenum targets and its large-scale production for nuclear medical application
    • 94mTc from enriched molybdenum targets and its large-scale production for nuclear medical application. Radiochim. Acta 64, 113-120.
    • (1994) Radiochim. Acta , vol.64 , pp. 113-120
    • Roesch, F.1    Novgorodov, A.F.2    Qaim, S.M.3
  • 44
    • 85123225078 scopus 로고    scopus 로고
    • 94Mo(p,n)-reaction
    • Erratum to document cited in Chem. Abstr. 120, 88184
    • 94Mo(p,n)-reaction. [Erratum to document cited in Chem. Abstr. 120, 88184]. Radiochim. Acta 75, 227.
    • (1996) Radiochim. Acta , vol.75 , pp. 227
    • Roesch, F.1    Qaim, S.M.2
  • 45
    • 0034185878 scopus 로고    scopus 로고
    • 94mTc for positron emission tomography studies
    • 94mTc for positron emission tomography studies. Nucl. Med. Biol. 27, 323-328.
    • (2000) Nucl. Med. Biol. , vol.27 , pp. 323-328
    • Qaim, S.M.1
  • 46
    • 0001738153 scopus 로고
    • Photochemistry of vinyl halides. Vinyl cation from photolysis of 1,1-diaryl-2-halopropenes
    • Kitamura, T., Kobayashi, S., and Taniguchi, H. (1982) Photochemistry of vinyl halides. Vinyl cation from photolysis of 1,1-diaryl-2-halopropenes. J. Org. Chem. 47, 2323-2328.
    • (1982) J. Org. Chem. , vol.47 , pp. 2323-2328
    • Kitamura, T.1    Kobayashi, S.2    Taniguchi, H.3
  • 47
    • 0015902629 scopus 로고
    • Photoaffinity labels for estrogen binding proteins of rat uterus
    • Katzenellenbogen, J. A., Johnson, H. J., Jr., and Myers, H. N. (1973) Photoaffinity labels for estrogen binding proteins of rat uterus. Biochemistry 12, 4085-4092.
    • (1973) Biochemistry , vol.12 , pp. 4085-4092
    • Katzenellenbogen, J.A.1    Johnson Jr., H.J.2    Myers, H.N.3
  • 48
    • 0030734795 scopus 로고    scopus 로고
    • Altered ligand binding properties and enhanced stability of a constitutively active estrogen receptor: Evidence that an open pocket conformation is required for ligand interaction
    • Carlson, K. E., Choi, I., Gee, A., Katzenellenbogen, B. S., and Katzenellenbogen, J. A. (1997) Altered ligand binding properties and enhanced stability of a constitutively active estrogen receptor: evidence that an open pocket conformation is required for ligand interaction. Biochemistry 36, 14897-14905.
    • (1997) Biochemistry , vol.36 , pp. 14897-14905
    • Carlson, K.E.1    Choi, I.2    Gee, A.3    Katzenellenbogen, B.S.4    Katzenellenbogen, J.A.5
  • 53
    • 0007953038 scopus 로고
    • High-temperature oxide and hydroxide vapor species of technetium
    • Gibson, J. K. (1993) High-temperature oxide and hydroxide vapor species of technetium. Radiochim. Acta 60, 121-126.
    • (1993) Radiochim. Acta , vol.60 , pp. 121-126
    • Gibson, J.K.1
  • 55
    • 15244349449 scopus 로고    scopus 로고
    • Preparation of 2,2-(diaryl)vinylphosphine compounds, palladium catalyst thereof, and a process for producing arylamine, diaryl, or arylalkyne with the catalyst. EP 1167372, 42 pp
    • Suzuki, K., Kobayashi, T., Nishikawa, T., Hori, Y., and Hagiwara, T. (2002) Preparation of 2,2-(diaryl)vinylphosphine compounds, palladium catalyst thereof, and a process for producing arylamine, diaryl, or arylalkyne with the catalyst. EP 1167372, 42 pp.
    • (2002)
    • Suzuki, K.1    Kobayashi, T.2    Nishikawa, T.3    Hori, Y.4    Hagiwara, T.5
  • 56
    • 15244361876 scopus 로고
    • Synthesis and deprotection of [1-(ethoxycarbonyl)-4-[(diphenylmethoxy)- carbonyl]-1-methyl-2-oxobutyl]triphenylphosphonium chloride: A key intermediate in the Wittig reaction between a cyclic anhydride and a stabilized ylide
    • Abell, A. D., Morris, K. B. and Litten, J. C. (1990) Synthesis and deprotection of [1-(ethoxycarbonyl)-4-[(diphenylmethoxy)-carbonyl]-1-methyl-2- oxobutyl]triphenylphosphonium chloride: a key intermediate in the Wittig reaction between a cyclic anhydride and a stabilized ylide. J. Org. Chem. 55, 5217-5221.
    • (1990) J. Org. Chem. , vol.55 , pp. 5217-5221
    • Abell, A.D.1    Morris, K.B.2    Litten, J.C.3
  • 57
    • 0001186167 scopus 로고
    • Synthesis and thermal properties of mesomorphic 1, 1′-bis[w- (4′-cyano-4-biphenyloxy)alkyl]ferrocenes
    • Bhatt, J., Fung, B. M., and Nicholas, K. M. (1992) Synthesis and thermal properties of mesomorphic 1, 1′-bis[w-(4′-cyano-4-biphenyloxy)alkyl] ferrocenes. Liq. Cryst. 12, 263-272.
    • (1992) Liq. Cryst. , vol.12 , pp. 263-272
    • Bhatt, J.1    Fung, B.M.2    Nicholas, K.M.3
  • 58
    • 15244355963 scopus 로고
    • Ph.D. Dissertation, Freien Universitat Berlin, Berlin, Germany
    • Kuntschke, D. (1994) Ph.D. Dissertation, Freien Universitat Berlin, Berlin, Germany.
    • (1994)
    • Kuntschke, D.1
  • 59
    • 0032814407 scopus 로고    scopus 로고
    • Synthesis of cyclopentadienyl tricarbonyl technetium phenyltropane derivatives by direct double ligand transfer with ferrocene precursors
    • Cesati, R. R., III, Tamagnan, G., Baldwin, R. M., Zoghbi, S. S., Innis, R. B., and Katzenellenbogen, J. A. (1999) Synthesis of cyclopentadienyl tricarbonyl technetium phenyltropane derivatives by direct double ligand transfer with ferrocene precursors. J. Labelled Compd. Radiopharm. 42, S150-S152.
    • (1999) J. Labelled Compd. Radiopharm. , vol.42
    • Cesati III, R.R.1    Tamagnan, G.2    Baldwin, R.M.3    Zoghbi, S.S.4    Innis, R.B.5    Katzenellenbogen, J.A.6


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