References
- Ametamey, S. M.; Honer, M.; Schubiger, P. A. Chem. Rev. 2008, 108, 1501-1516. https://doi.org/10.1021/cr0782426
- Miller, P. W.; Long, N. J.; Vilar, R.; Gee, A. D. Angew. Chem. Int. Ed. 2008, 47, 8998-9033. https://doi.org/10.1002/anie.200800222
- Cai, L.; Lu, S.; Pike, V. W. Eur. J. Org. Chem. 2008, 2853-2873.
- Moon, B. S.; Park, J. H.; Lee, H. J.; Kim, J. S.; Kil, H. S.; Lee, B.S.; Chi, D. Y.; Lee, B. C.; Kim, Y. K.; Kim, S. E. Appl. Radiat. Isot. 2010, 68, 2279-2284. https://doi.org/10.1016/j.apradiso.2010.06.016
- Lee, B. S.; Seo, J. W.; Lee, S. J.; Oh, S. J.; Chi, D. Y. Bull. Korean Chem. Soc. 2011, 32, 71-76. https://doi.org/10.5012/bkcs.2011.32.1.71
- Kim, D. W.; Ahn, D. S.; Oh, Y. H.; Lee, S.; Kil, H. S.; Oh, S. J.; Lee, S. J.; Kim, J. S.; Ryu, J. S.; Moon, D. H.; Chi, D. Y. Am. Chem. Soc. 2006, 128, 16394-16397. https://doi.org/10.1021/ja0646895
- Lee, S. J.; Oh, S. J.; Chi, D. Y.; Lee, B. S.; Ryu, J. S.; Moon, D. H. J. Labelled Compd. Radiopharm. 2008, 51, 80-82. https://doi.org/10.1002/jlcr.1478
- Lee, S. J.; Oh, S. J.; Chi, D. Y.; Kil, H. S.; Kim, E. N.; Ryu, J. S.; Moon, D. H. Eur. J. Nucl. Med. Mol. Imaging. 2007, 34, 1406- 1409. https://doi.org/10.1007/s00259-007-0391-8
- Suehiro, M.; Vallabhajosula, S.; Goldsmith, S. J.; Ballon, D. J. Appl. Radiat. Isot. 2007, 65, 1350-1358. https://doi.org/10.1016/j.apradiso.2007.07.013
- Nishijima, K.; Kuge, Y.; Tsukamoto, E.; Seki, K.; Ohkura, K.; Magata, Y.; Tanaka, A.; Nagatsu, K.; Tamaki, N. Appl. Radiat. Isot. 2002, 57, 43-49. https://doi.org/10.1016/S0969-8043(02)00070-2
- Huang, B. X.; Channing, M. A.; Plascjak, P. S.; Kiesewetter, D. O.; Der, M.; Ma, Y.; Eckelman, W. C. Nucl. Med. Biol. 2003, 30, 785-790. https://doi.org/10.1016/S0969-8051(03)00083-0
- Hayashi, K.; Furutsuka, K.; Takei, M.; Muto, M.; Nakao, R.; Aki, H.; Suzuki, K.; Fukumura, T. Appl. Radiat. Isot. 2011, 69, 1007- 1013. https://doi.org/10.1016/j.apradiso.2011.02.025
- Lee, S. J.; Oh, S. J.; Moon, W. Y.; Choi, M. S.; Kim, J. S.; Chi, D. Y.; Moon, D. H.; Ryu, J. S. Nucl. Med. Biol. 2011, 38, 593-597. https://doi.org/10.1016/j.nucmedbio.2010.11.012
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