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Autor:
Raisa Krasikova, Ch. V. Chang, Viktoriya Orlovskaya, Ch. L. Chen, Yu. N. Belokon, R. Sh. Liu, T. F. Savel'eva, Olga S. Fedorova, Victor I. Maleev
Publikováno v:
Russian Chemical Bulletin. 63:1169-1177
An asymmetric synthesis method has been suggested as a feasible approach for the preparation of fluorine-18-labeled (T1/2 110 min) analog of l-threo-3,4-dihydroxyphenylserine, i.e., 6-l-threo-[18F]FDOPS ((2S,3R)-2-amino-3-(2-[18F]fluoro-4,5-dihydroxy