Nucleophilic [18F]Fluorination and subsequent decarbonylation of methoxy-substituted nitro- and halogen-benzenes activated by one or two formyl groups

Journal of Labelled Compounds and Radiopharmaceuticals

Volumn 53, Issue 3, 2010, Pages 113-119

  Shen, Bin ^a   Löffler, Dirk ^a   Reischl, Gerald ^a   Machulla, Hans Jürgen ^a   Zeller, Klaus Peter ^a  

^a UNIVERSITY OF TÜBINGEN   (Germany)

Author keywords

Benzaldehyde; Decarbonylation; Nucleophilic substitution

Indexed keywords

AMINO ACIDS; AROMATIC COMPOUNDS; FLUORINE COMPOUNDS; REACTION RATES;

AROMATIC AMINO ACID; BENZALDEHYDE; DECARBONYLATIONS; FORMYL GROUP; HIGHER YIELD; ISOPHTHALALDEHYDES; METHOXY; MODEL REACTIONS; NUCLEOPHILIC SUBSTITUTIONS; RADIOCHEMICAL YIELD;

ALDEHYDES;

2 FLUORO 5 METHOXYISOPHTHALALDEHYDE F 18; 2 ISOPHTHALALDEHYDE DERIVATIVE; 2 TEREPHTHALALDEHYDE DERIVATIVE; 4 FLUORO 2 METHOXY 5 METHYLISOPHTHALALDEHYDE F 18; BENZENE DERIVATIVE; FLUORINE 18; RADIOPHARMACEUTICAL AGENT; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; DECARBONYLATION; DRUG SYNTHESIS; FLUORINATION; REACTION ANALYSIS;

EID: 77950397250     PISSN: 03624803     EISSN: 10991344     Source Type: Journal    
DOI: 10.1002/jlcr.1736     Document Type: Article

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