Semiautomatic synthesis of 3′-deoxy-3′-[18F] fluorothymidine using three precursors

Applied Radiation and Isotopes

Volumn 64, Issue 2, 2006, Pages 187-193

  Teng, Bao ^a   Wang, Shizhen ^a   Fu, Zhe ^a   Dang, Yonghong ^a   Wu, Zhanhong ^a   Liu, Liqin ^a  

^a PEKING UNION MEDICAL COLLEGE HOSPITAL   (China)

Author keywords

18F fluoride; 18F FLT; Proliferation; Semiautomatic synthesis; Thymidine

Indexed keywords

DERIVATIVES; RADIOLYSIS; SYNTHESIS (CHEMICAL);

[18F] FLUORIDE; [18F]FLT; PROLIFERATION; SEMIAUTOMATIC SYNTHESIS;

FLUORINE COMPOUNDS;

3 N TERT BUTOXYCARBONYL[5' O (4,4' DIMETHOXYTRITYL) 2' DEOXY 3' O (4 NITROBENZENESULFONYL) BETA THREO PENTOFURANOSYL]THYMINE; 3' DEOXY 3' FLUOROTHYMIDINE F18; 3' FLUOROTHYMIDINE; FLUORODEOXYGLUCOSE F 18; THYMINE DERIVATIVE; TRACER; UNCLASSIFIED DRUG;

ARTICLE; AUTOMATION; CHEMICAL MODIFICATION; DRUG MANUFACTURE; DRUG SYNTHESIS; PRECURSOR; PRIORITY JOURNAL; QUANTUM YIELD; RADIOCHEMISTRY; REPRODUCIBILITY; TIME;

CHROMATOGRAPHY, GAS; DIDEOXYNUCLEOSIDES; FLUORINE RADIOISOTOPES; MAGNETIC RESONANCE SPECTROSCOPY; POSITRON-EMISSION TOMOGRAPHY; RADIOPHARMACEUTICALS;

EID: 28044456342     PISSN: 09698043     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.apradiso.2005.07.017     Document Type: Article

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