Radiohalogen incorporation into organic systems

被引:42
作者
Bolton, R [1 ]
机构
[1] Univ Surrey, Sch Phys Sci, Dept Chem, Surrey GU2 7XG, England
关键词
radiohalogen; bromine; fluorine; iodine; substitution; halogeno-demetallation;
D O I
10.1002/jlcr.575
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This Review reports the more recent applications of radiohalogen labelling in organic compounds. Modern synthetic methods place more emphasis upon substitution at specific sites. Electrophilic substitution, especially at aromatic carbon atoms, involves displacement of halogen or of metals rather than the earlier popular halogen-deprotiation processes. Nucleophilic displacement, at either aliphatic or aromatic sites, has also become widespread since it may be made more selective by the inclusion of appropriate activating groups or suitable displaced groups. Microwave and thermally induced methods are both reported with a critical assessment of the value of each process. Copyright (C) 2002 John Wiley Sons, Ltd.
引用
收藏
页码:485 / 528
页数:44
相关论文
共 283 条
[1]  
ADAM MJ, 1984, J LABELLED COMPD RAD, V21, P1227
[2]   SYNTHESIS AND SEPARATION OF 3-O-METHYL-2-FLUORODOPA AND 6-[F-18]-FLUORODOPA [J].
ADAM, MJ ;
JIVAN, S .
JOURNAL OF LABELLED COMPOUNDS & RADIOPHARMACEUTICALS, 1992, 31 (01) :39-43
[3]   SYNTHESIS OF N,N-DIMETHYL-[BETA-(3,4-DIACETOXY-6-I-123-IODOPHENYL)]-ETHYLAMINE (IDDE) - A POTENTIAL RADIOTRACER FOR THE STUDY OF THE DOPAMINERGIC SYSTEM [J].
ADAM, MJ ;
PONCE, YZ ;
BERRY, JM ;
LU, JM .
JOURNAL OF LABELLED COMPOUNDS & RADIOPHARMACEUTICALS, 1992, 31 (01) :3-10
[4]  
Adam MJ, 1999, J LABELLED COMPD RAD, V42, P809
[5]   STEREOSELECTIVE SYNTHESIS OF 3-O-METHYL-6-[F-18]FLUORODOPA VIA FLUORODESTANNYLATION [J].
ADAM, MJ ;
LU, JM ;
JIVAN, S .
JOURNAL OF LABELLED COMPOUNDS & RADIOPHARMACEUTICALS, 1994, 34 (06) :565-570
[6]  
Aigbirhio FI, 1997, J LABELLED COMPD RAD, V39, P567, DOI 10.1002/(SICI)1099-1344(199707)39:7<567::AID-JLCR999>3.0.CO
[7]  
2-P
[8]  
Akula MR, 1999, J LABELLED COMPD RAD, V42, P959, DOI 10.1002/(SICI)1099-1344(199910)42:10<959::AID-JLCR254>3.0.CO
[9]  
2-M
[10]  
Al-Qahtani M. H., 2001, Journal of Labelled Compounds and Radiopharmaceuticals, V44, pS305