Radiosynthesis of F-18 labeled cytidine analog 2′-fluoro-5-iodo-l-β-d-arabinofuranosylcytosine ([18F]FIAC)

Applied Radiation and Isotopes

Volumn 67, Issue 7-8, 2009, Pages 1362-1365

  Wu, Chun Yi ^a   Chan, Pei Chia ^a   Chang, Wei Ting ^a   Liu, Ren Shyan ^a,b   Alauddin, Mian M ^c   Wang, Hsin Ell ^a  

^a NATIONAL YANG MING UNIVERSITY   (Taiwan)

^b TAIPEI VETERANS GENERAL HOSPITAL   (Taiwan)

^c UNIVERSITY OF TEXAS MD ANDERSON CANCER CENTER   (United States)

Author keywords

FIAC; Fluorine 18

Indexed keywords

2-DEOXY-2; CRUDE PRODUCTS; CYTIDINE; DICHLOROETHANE; FIAC; FLUORINE-18; RADIOCHEMICAL PURITY; RADIOCHEMICAL YIELD; RADIOSYNTHESIS; SILYL ETHERS; SODIUM METHOXIDE;

ACETONITRILE; ETHERS; RADIOISOTOPES; SILANES; SODIUM;

FLUORINE;

1,2 DICHLOROETHANE; ACETONITRILE; CYTIDINE DERIVATIVE; FIACITABINE F 18; RADIOISOTOPE; UNCLASSIFIED DRUG;

ARTICLE; DRUG PURIFICATION; DRUG SELECTIVITY; DRUG STRUCTURE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HYDROLYSIS; ISOTOPE LABELING; PRIORITY JOURNAL; PROCESS OPTIMIZATION; RADIOACTIVITY; RADIOCHEMISTRY; STRUCTURE ANALYSIS; SYNTHESIS;

CYTARABINE; CYTIDINE; FLUORINE RADIOISOTOPES; ISOTOPE LABELING; RADIOPHARMACEUTICALS;

EID: 67349285111     PISSN: 09698043     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.apradiso.2009.02.083     Document Type: Article

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