@article{oai:repo.qst.go.jp:00047694,
 author = {Fukumura, Toshimitsu and Takei, Makoto and Suzuki, Kazutoshi and 福村 利光 and 武井 誠 and 鈴木 和年},
 issue = {12},
 journal = {Applied Radiation and Isotopes},
 month = {Dec},
 note = {No-carrier-added 2-[(34m)Cl]chloro-2-deoxy-d-glucose ([(34m)Cl]ClDG) was prepared via nucleophilic displacement reaction of 1, 3, 4, 6-tetra-O-acetyl-2-trifluoromethansulfonyl mannose with K[(34m)Cl]Cl/kryptofix 222 complex using (34m)Cl(-) produced via the (nat)S(alpha, 2n) nuclear reactions. The synthesis time from enrichment of [(34m)Cl]Cl(-) was approximately 45min and the radiochemical yield was 79.6+/-6.7% (n=3) with decay correction. Animal PET studies showed that the behavior of [(34m)Cl]ClDG was quite different from that of [(18)F]FDG. [(34m)Cl]ClDG did not accumulate in any organ and was excreted as [(34m)Cl]ClDG.},
 pages = {1905--1909},
 title = {Synthesis  and biodistribution of 34mCl-labeled 2-chloro-2-deoxy-D-glucose:A major impurity in[18F]FDG injection},
 volume = {66},
 year = {2008}
}