Aliphatic 18 F-Radiofluorination: Recent Advances in the Labeling of Base-Sensitive Substrates

Aliphatic fluorine-18 radiolabeling is the most commonly used method to synthesize tracers for PET-imaging. With an increasing demand for F-radiotracers for clinical applications, new labeling strategies aiming to increase radiochemical yields of established tracers or, more importantly, to enable F...

Full description

Saved in:
Bibliographic Details
Published inChemMedChem Vol. 16; no. 17; pp. 2612 - 2622
Main Authors Bratteby, Klas, Shalgunov, Vladimir, Herth, Matthias Manfred
Format Journal Article
LanguageEnglish
Published Germany 06.09.2021
Subjects
Online AccessGet full text

Cover

Loading…
Abstract Aliphatic fluorine-18 radiolabeling is the most commonly used method to synthesize tracers for PET-imaging. With an increasing demand for F-radiotracers for clinical applications, new labeling strategies aiming to increase radiochemical yields of established tracers or, more importantly, to enable F-labeling of new scaffolds have been developed. In recent years, increased attention has been focused on the direct aliphatic F-fluorination of base-sensitive substrates in this respect. This minireview gives a concise overview of the recent advances within this field and aims to highlight the advantages and limitations of these methods.
AbstractList Aliphatic fluorine‐18 radiolabeling is the most commonly used method to synthesize tracers for PET‐imaging. With an increasing demand for 18 F‐radiotracers for clinical applications, new labeling strategies aiming to increase radiochemical yields of established tracers or, more importantly, to enable 18 F‐labeling of new scaffolds have been developed. In recent years, increased attention has been focused on the direct aliphatic 18 F‐fluorination of base‐sensitive substrates in this respect. This minireview gives a concise overview of the recent advances within this field and aims to highlight the advantages and limitations of these methods.
Aliphatic fluorine-18 radiolabeling is the most commonly used method to synthesize tracers for PET-imaging. With an increasing demand for F-radiotracers for clinical applications, new labeling strategies aiming to increase radiochemical yields of established tracers or, more importantly, to enable F-labeling of new scaffolds have been developed. In recent years, increased attention has been focused on the direct aliphatic F-fluorination of base-sensitive substrates in this respect. This minireview gives a concise overview of the recent advances within this field and aims to highlight the advantages and limitations of these methods.
Author Bratteby, Klas
Shalgunov, Vladimir
Herth, Matthias Manfred
Author_xml – sequence: 1
  givenname: Klas
  surname: Bratteby
  fullname: Bratteby, Klas
  organization: Department of Clinical Physiology, Nuclear Medicine & PET Rigshospitalet, Blegdamsvej 9, 2100, Copenhagen, Denmark
– sequence: 2
  givenname: Vladimir
  surname: Shalgunov
  fullname: Shalgunov, Vladimir
  organization: Department of Drug Design and Pharmacology Faculty of Health and Medical Sciences, University of Copenhagen, Jagtvej 160, 2100, Copenhagen, Denmark
– sequence: 3
  givenname: Matthias Manfred
  orcidid: 0000-0002-7788-513X
  surname: Herth
  fullname: Herth, Matthias Manfred
  organization: Department of Clinical Physiology, Nuclear Medicine & PET Rigshospitalet, Blegdamsvej 9, 2100, Copenhagen, Denmark
BackLink https://www.ncbi.nlm.nih.gov/pubmed/34169672$$D View this record in MEDLINE/PubMed
BookMark eNo9kM1PwjAYhxuDEUGvHk2PXob92tZ6QyJqQmICenVpu7dSMzpcNxL_e0dATu9HnveXN88IDUIdAKEbSiaUEHZvN6WdMML6gRN-hi6pzEiSU5kPTn2uhmgU4zchQkgqL9CQC5qpLGeX6HNa-e1at95iKvE8WerS167q6saHfluHB7wEC6HF03Kng4WIfcDtGvBCG6h8-MK1w486QrKCEH3rd4BXnYlto1uIV-jc6SrC9bGO0cf86X32kizenl9n00ViqSAsUSntX5I6zUpugDHHhDOZyqUjnEsqWGm0sWlugRhJS-MUFynNMmLznGal42N0d8jdNvVPB7EtNj5aqCodoO5iwVKRpkqoVPXo5IDapo6xAVdsG7_RzW9BSbF3WuydFien_cHtMbszGyhP-L9E_gcbHHL2
CitedBy_id crossref_primary_10_1134_S1066362223020030
crossref_primary_10_3390_app12010321
crossref_primary_10_1021_jacs_3c04548
crossref_primary_10_3390_ph15060685
crossref_primary_10_3390_molecules28030931
crossref_primary_10_1002_ajoc_202300412
crossref_primary_10_1021_jacs_3c01824
crossref_primary_10_1002_tcr_202300072
crossref_primary_10_3390_ph15101191
crossref_primary_10_1039_D3QO00772C
crossref_primary_10_31857_S003383112302003X
crossref_primary_10_1002_chem_202202965
crossref_primary_10_1038_s41598_023_30200_2
crossref_primary_10_1002_jlcr_4018
Cites_doi 10.1155/2014/672094
10.1016/j.neuropharm.2019.107830
10.1021/acs.accounts.5b00062
10.1021/cr0782426
10.1177/0271678X20905433
10.1002/jlcr.3191
10.1021/acsomega.7b01374
10.1053/j.semnuclmed.2020.09.004
10.1016/j.nucmedbio.2020.11.003
10.1053/j.semnuclmed.2003.12.002
10.1016/j.apradiso.2020.109195
10.1016/j.nucmedbio.2020.07.003
10.1002/jlcr.1742
10.1002/ange.201805501
10.1039/C9CC00641A
10.1007/s00259-003-1330-y
10.1016/j.atherosclerosis.2017.03.014
10.1002/anie.198106471
10.1002/anie.201805501
10.1021/acs.chemrev.5b00493
10.1039/C8CC03206H
10.1038/nchem.1280
10.1016/j.neuroimage.2011.12.037
10.1039/c2cc38646a
10.1016/j.ejmech.2020.113046
10.2967/jnumed.118.218495
10.1016/j.apradiso.2017.04.021
10.1021/mp4004817
10.1016/j.mibio.2003.09.011
10.1039/C4OB01336K
10.1016/j.nucmedbio.2018.06.004
10.1055/s-0039-1690012
10.1021/bc500475e
10.1016/B978-012744482-6.50026-0
10.1016/j.nucmedbio.2012.12.010
10.1016/j.jfluchem.2013.09.006
10.1016/S0969-8051(98)00070-5
10.1007/978-3-319-98947-1_17
10.1016/B978-0-12-812958-6.00002-1
10.1021/jacs.7b03131
10.1016/j.nucmedbio.2017.09.004
10.1002/jlcr.1931
10.1002/anie.201206566
10.2174/1874471011003020081
10.1016/j.addr.2010.09.007
10.1038/s41598-017-00110-1
10.1038/nchem.1756
10.1007/978-3-540-49527-7_11
10.1002/chem.201100458
10.1021/ol403017e
10.1016/j.bmcl.2007.12.054
10.1039/c0cc03078c
10.1016/j.apradiso.2014.04.021
10.1002/chem.201803261
10.1007/s40336-018-0280-0
10.1039/C4SC02099E
10.1039/C7SC04545J
10.1016/S0969-8051(97)00078-4
10.1002/ange.201201502
10.26434/chemrxiv.14229491.v1
10.1002/ejoc.200800114
10.1002/jlcr.572
10.1016/j.apradiso.2007.07.013
10.1007/s40336-020-00368-y
10.1002/anie.201201502
10.1039/C8CS00499D
10.1021/jo00890a018
10.1016/j.critrevonc.2020.103044
10.1002/ejoc.202000056
10.1021/ja5025645
10.5012/bkcs.2012.33.7.2177
10.1002/chem.201900930
10.1016/j.apradiso.2012.10.011
10.1016/S0969-8043(98)00106-7
10.1007/s11307-019-01337-2
10.5012/bkcs.2011.32.1.71
10.3390/molecules22122231
10.1021/jacs.6b06770
10.1002/ange.201206566
10.1016/j.nucmedbio.2010.04.185
10.1016/j.apradiso.2019.07.006
10.1039/C8CC00526E
10.1016/j.apradiso.2009.09.071
10.1021/ja0646895
10.1021/op400349g
10.1016/j.nucmedbio.2010.11.012
10.1016/j.nucmedbio.2011.04.006
10.1016/j.jfluchem.2015.09.012
10.1371/journal.pone.0059187
10.1007/978-3-319-98947-1_16
10.1038/s41598-018-37186-2
10.1007/978-3-319-98947-1_15
10.1039/C9CC02779C
10.1053/snuc.2000.7439
ContentType Journal Article
Copyright 2021 Wiley-VCH GmbH.
Copyright_xml – notice: 2021 Wiley-VCH GmbH.
DBID CGR
CUY
CVF
ECM
EIF
NPM
AAYXX
CITATION
7X8
DOI 10.1002/cmdc.202100303
DatabaseName Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
CrossRef
MEDLINE - Academic
DatabaseTitle MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
CrossRef
MEDLINE - Academic
DatabaseTitleList CrossRef
MEDLINE
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Pharmacy, Therapeutics, & Pharmacology
EISSN 1860-7187
EndPage 2622
ExternalDocumentID 10_1002_cmdc_202100303
34169672
Genre Research Support, Non-U.S. Gov't
Journal Article
Review
GrantInformation_xml – fundername: Innovation Fund Denmark
– fundername: Faculty of Health and Medical Sciences, University of Copenhagen
– fundername: Lundbeck Foundation
– fundername: Research Council for Independent Research
– fundername: Novo Nordisk Foundation
  grantid: NNF18SA0034956
GroupedDBID ---
05W
0R~
1L6
1OC
29B
33P
3WU
4.4
53G
5GY
66C
6J9
77Q
8-0
8-1
A00
AAESR
AAHHS
AANLZ
AAXRX
AAZKR
ABCUV
ABIJN
ABJNI
ABLJU
ACAHQ
ACCFJ
ACCZN
ACGFS
ACIWK
ACPOU
ACPRK
ACXBN
ACXQS
ADBBV
ADKYN
ADMGS
ADOZA
ADXAS
ADZMN
ADZOD
AEEZP
AEGXH
AEIGN
AENEX
AEQDE
AEUQT
AEUYR
AFBPY
AFFPM
AFGKR
AFRAH
AHBTC
AHMBA
AITYG
AIURR
AIWBW
AJBDE
ALMA_UNASSIGNED_HOLDINGS
ALUQN
AMYDB
AZVAB
BDRZF
BFHJK
BMXJE
BRXPI
CGR
CS3
CUY
CVF
DCZOG
DR2
DRFUL
DRSTM
DU5
EBD
EBS
ECM
EIF
EMOBN
F5P
G-S
HBH
HGLYW
HHZ
HZ~
IX1
LATKE
LAW
LEEKS
LH4
LITHE
LOXES
LUTES
LYRES
MEWTI
MXFUL
MXSTM
MY~
NPM
O9-
OIG
P2W
P4E
PQQKQ
ROL
RWI
SUPJJ
SV3
W99
WBKPD
WOHZO
WXSBR
WYJ
XV2
YZZ
ZZTAW
~S-
AAMNL
AAYXX
CITATION
7X8
ID FETCH-LOGICAL-c1402-9513418a56d3be22f24fb6978f0338142dbabc57ce0b81dbf93451660c7716df3
ISSN 1860-7179
IngestDate Wed Dec 04 00:00:25 EST 2024
Fri Dec 06 03:00:49 EST 2024
Sat Sep 28 08:22:30 EDT 2024
IsPeerReviewed true
IsScholarly true
Issue 17
Keywords aliphatic
fluorine-18
SN2
base sensitivity
radiochemistry
Language English
License 2021 Wiley-VCH GmbH.
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-c1402-9513418a56d3be22f24fb6978f0338142dbabc57ce0b81dbf93451660c7716df3
Notes ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-3
content type line 23
ObjectType-Review-1
ORCID 0000-0002-7788-513X
PMID 34169672
PQID 2545594959
PQPubID 23479
PageCount 11
ParticipantIDs proquest_miscellaneous_2545594959
crossref_primary_10_1002_cmdc_202100303
pubmed_primary_34169672
PublicationCentury 2000
PublicationDate 2021-09-06
20210906
PublicationDateYYYYMMDD 2021-09-06
PublicationDate_xml – month: 09
  year: 2021
  text: 2021-09-06
  day: 06
PublicationDecade 2020
PublicationPlace Germany
PublicationPlace_xml – name: Germany
PublicationTitle ChemMedChem
PublicationTitleAlternate ChemMedChem
PublicationYear 2021
References e_1_2_7_3_1
Garcia Vazquez R. (e_1_2_7_41_1) 2020; 61
e_1_2_7_7_1
e_1_2_7_19_1
e_1_2_7_60_1
e_1_2_7_83_1
e_1_2_7_64_1
e_1_2_7_87_1
e_1_2_7_11_1
e_1_2_7_45_1
e_1_2_7_68_1
e_1_2_7_49_1
e_1_2_7_90_2
e_1_2_7_90_1
e_1_2_7_94_1
e_1_2_7_71_1
e_1_2_7_52_1
Ermert J. (e_1_2_7_46_1) 2019
e_1_2_7_23_1
e_1_2_7_33_1
e_1_2_7_75_1
e_1_2_7_56_1
Wagner M. (e_1_2_7_29_1) 2019
e_1_2_7_37_1
e_1_2_7_79_1
e_1_2_7_4_1
e_1_2_7_8_1
e_1_2_7_16_1
e_1_2_7_40_1
e_1_2_7_82_1
e_1_2_7_63_1
e_1_2_7_12_1
e_1_2_7_44_1
e_1_2_7_86_1
e_1_2_7_67_1
e_1_2_7_48_1
e_1_2_7_51_1
e_1_2_7_70_1
e_1_2_7_93_1
e_1_2_7_24_1
e_1_2_7_32_1
e_1_2_7_55_1
e_1_2_7_74_1
e_1_2_7_20_1
e_1_2_7_36_1
e_1_2_7_59_1
e_1_2_7_78_1
e_1_2_7_5_1
e_1_2_7_9_1
e_1_2_7_17_1
e_1_2_7_62_1
e_1_2_7_81_1
e_1_2_7_81_2
e_1_2_7_13_1
e_1_2_7_43_1
e_1_2_7_66_1
e_1_2_7_85_1
e_1_2_7_47_1
e_1_2_7_89_1
e_1_2_7_28_1
Morris E. D. (e_1_2_7_26_1) 2004
e_1_2_7_73_1
e_1_2_7_50_1
e_1_2_7_92_1
e_1_2_7_25_1
e_1_2_7_31_1
e_1_2_7_77_1
e_1_2_7_31_2
e_1_2_7_54_1
e_1_2_7_21_1
e_1_2_7_35_1
e_1_2_7_58_1
e_1_2_7_39_1
e_1_2_7_6_1
e_1_2_7_80_1
e_1_2_7_18_1
e_1_2_7_84_1
e_1_2_7_61_1
e_1_2_7_2_1
e_1_2_7_14_1
e_1_2_7_42_1
e_1_2_7_88_1
Meyer J. H. (e_1_2_7_1_1) 2020; 7
e_1_2_7_65_1
e_1_2_7_10_1
e_1_2_7_69_1
e_1_2_7_27_1
e_1_2_7_91_1
Edem P. E. (e_1_2_7_15_1) 2019
e_1_2_7_72_1
e_1_2_7_95_1
e_1_2_7_30_1
e_1_2_7_53_1
e_1_2_7_76_1
e_1_2_7_22_1
e_1_2_7_34_1
e_1_2_7_57_1
e_1_2_7_38_1
References_xml – ident: e_1_2_7_14_1
  doi: 10.1155/2014/672094
– ident: e_1_2_7_8_1
  doi: 10.1016/j.neuropharm.2019.107830
– ident: e_1_2_7_83_1
  doi: 10.1021/acs.accounts.5b00062
– ident: e_1_2_7_7_1
  doi: 10.1021/cr0782426
– ident: e_1_2_7_27_1
  doi: 10.1177/0271678X20905433
– ident: e_1_2_7_50_1
  doi: 10.1002/jlcr.3191
– ident: e_1_2_7_62_1
  doi: 10.1021/acsomega.7b01374
– ident: e_1_2_7_6_1
  doi: 10.1053/j.semnuclmed.2020.09.004
– ident: e_1_2_7_42_1
  doi: 10.1016/j.nucmedbio.2020.11.003
– ident: e_1_2_7_10_1
  doi: 10.1053/j.semnuclmed.2003.12.002
– ident: e_1_2_7_70_1
  doi: 10.1016/j.apradiso.2020.109195
– ident: e_1_2_7_11_1
  doi: 10.1016/j.nucmedbio.2020.07.003
– ident: e_1_2_7_48_1
  doi: 10.1002/jlcr.1742
– ident: e_1_2_7_31_2
  doi: 10.1002/ange.201805501
– ident: e_1_2_7_80_1
  doi: 10.1039/C9CC00641A
– ident: e_1_2_7_13_1
  doi: 10.1007/s00259-003-1330-y
– ident: e_1_2_7_9_1
  doi: 10.1016/j.atherosclerosis.2017.03.014
– ident: e_1_2_7_55_1
  doi: 10.1002/anie.198106471
– ident: e_1_2_7_68_1
– ident: e_1_2_7_31_1
  doi: 10.1002/anie.201805501
– ident: e_1_2_7_34_1
  doi: 10.1021/acs.chemrev.5b00493
– ident: e_1_2_7_76_1
  doi: 10.1039/C8CC03206H
– ident: e_1_2_7_93_1
  doi: 10.1038/nchem.1280
– ident: e_1_2_7_4_1
  doi: 10.1016/j.neuroimage.2011.12.037
– ident: e_1_2_7_92_1
  doi: 10.1039/c2cc38646a
– ident: e_1_2_7_5_1
  doi: 10.1016/j.ejmech.2020.113046
– ident: e_1_2_7_63_1
  doi: 10.2967/jnumed.118.218495
– volume: 61
  start-page: 134
  year: 2020
  ident: e_1_2_7_41_1
  publication-title: J. Nucl. Med.
  contributor:
    fullname: Garcia Vazquez R.
– ident: e_1_2_7_59_1
  doi: 10.1016/j.apradiso.2017.04.021
– ident: e_1_2_7_39_1
  doi: 10.1021/mp4004817
– ident: e_1_2_7_22_1
  doi: 10.1016/j.mibio.2003.09.011
– ident: e_1_2_7_61_1
  doi: 10.1039/C4OB01336K
– volume: 7
  start-page: 1064
  year: 2020
  ident: e_1_2_7_1_1
  publication-title: The Lancet
  contributor:
    fullname: Meyer J. H.
– ident: e_1_2_7_20_1
  doi: 10.1016/j.nucmedbio.2018.06.004
– ident: e_1_2_7_86_1
  doi: 10.1055/s-0039-1690012
– ident: e_1_2_7_16_1
  doi: 10.1021/bc500475e
– start-page: 499
  volume-title: Emission Tomography. Fundamentals of PET and SPECT
  year: 2004
  ident: e_1_2_7_26_1
  doi: 10.1016/B978-012744482-6.50026-0
  contributor:
    fullname: Morris E. D.
– ident: e_1_2_7_19_1
  doi: 10.1016/j.nucmedbio.2012.12.010
– ident: e_1_2_7_73_1
  doi: 10.1016/j.jfluchem.2013.09.006
– ident: e_1_2_7_24_1
  doi: 10.1016/S0969-8051(98)00070-5
– ident: e_1_2_7_32_1
  doi: 10.1007/978-3-319-98947-1_17
– start-page: 29
  volume-title: Late-Stage Fluorination of Bioactive Molecules and Bioogically-Relevant Substrates
  year: 2019
  ident: e_1_2_7_15_1
  doi: 10.1016/B978-0-12-812958-6.00002-1
  contributor:
    fullname: Edem P. E.
– ident: e_1_2_7_40_1
  doi: 10.1021/jacs.7b03131
– ident: e_1_2_7_25_1
  doi: 10.1016/j.nucmedbio.2017.09.004
– ident: e_1_2_7_71_1
  doi: 10.1002/jlcr.1931
– ident: e_1_2_7_81_1
  doi: 10.1002/anie.201206566
– ident: e_1_2_7_58_1
  doi: 10.2174/1874471011003020081
– ident: e_1_2_7_30_1
  doi: 10.1016/j.addr.2010.09.007
– ident: e_1_2_7_67_1
  doi: 10.1038/s41598-017-00110-1
– ident: e_1_2_7_78_1
  doi: 10.1038/nchem.1756
– ident: e_1_2_7_64_1
  doi: 10.1007/978-3-540-49527-7_11
– ident: e_1_2_7_72_1
  doi: 10.1002/chem.201100458
– ident: e_1_2_7_85_1
  doi: 10.1021/ol403017e
– ident: e_1_2_7_51_1
  doi: 10.1016/j.bmcl.2007.12.054
– ident: e_1_2_7_57_1
  doi: 10.1039/c0cc03078c
– ident: e_1_2_7_45_1
  doi: 10.1016/j.apradiso.2014.04.021
– ident: e_1_2_7_53_1
  doi: 10.1002/chem.201803261
– ident: e_1_2_7_33_1
  doi: 10.1007/s40336-018-0280-0
– ident: e_1_2_7_36_1
  doi: 10.1039/C4SC02099E
– ident: e_1_2_7_84_1
  doi: 10.1039/C7SC04545J
– ident: e_1_2_7_28_1
  doi: 10.1016/S0969-8051(97)00078-4
– ident: e_1_2_7_90_1
  doi: 10.1002/ange.201201502
– ident: e_1_2_7_38_1
  doi: 10.26434/chemrxiv.14229491.v1
– ident: e_1_2_7_47_1
  doi: 10.1002/ejoc.200800114
– ident: e_1_2_7_49_1
  doi: 10.1002/jlcr.572
– ident: e_1_2_7_54_1
  doi: 10.1016/j.apradiso.2007.07.013
– ident: e_1_2_7_18_1
  doi: 10.1007/s40336-020-00368-y
– ident: e_1_2_7_90_2
  doi: 10.1002/anie.201201502
– ident: e_1_2_7_35_1
  doi: 10.1039/C8CS00499D
– ident: e_1_2_7_89_1
  doi: 10.1021/jo00890a018
– ident: e_1_2_7_2_1
  doi: 10.1016/j.critrevonc.2020.103044
– ident: e_1_2_7_79_1
  doi: 10.1002/ejoc.202000056
– ident: e_1_2_7_87_1
  doi: 10.1021/ja5025645
– ident: e_1_2_7_65_1
  doi: 10.5012/bkcs.2012.33.7.2177
– ident: e_1_2_7_75_1
  doi: 10.1002/chem.201900930
– ident: e_1_2_7_21_1
  doi: 10.1016/j.apradiso.2012.10.011
– ident: e_1_2_7_43_1
  doi: 10.1016/S0969-8043(98)00106-7
– ident: e_1_2_7_12_1
  doi: 10.1007/s11307-019-01337-2
– ident: e_1_2_7_69_1
  doi: 10.5012/bkcs.2011.32.1.71
– ident: e_1_2_7_60_1
  doi: 10.3390/molecules22122231
– ident: e_1_2_7_82_1
  doi: 10.1021/jacs.6b06770
– ident: e_1_2_7_81_2
  doi: 10.1002/ange.201206566
– ident: e_1_2_7_17_1
  doi: 10.1016/j.nucmedbio.2010.04.185
– ident: e_1_2_7_44_1
– ident: e_1_2_7_37_1
  doi: 10.1016/j.apradiso.2019.07.006
– ident: e_1_2_7_95_1
  doi: 10.1039/C8CC00526E
– ident: e_1_2_7_52_1
  doi: 10.1016/j.apradiso.2009.09.071
– ident: e_1_2_7_56_1
  doi: 10.1021/ja0646895
– ident: e_1_2_7_94_1
  doi: 10.1021/op400349g
– ident: e_1_2_7_66_1
  doi: 10.1016/j.nucmedbio.2010.11.012
– ident: e_1_2_7_23_1
  doi: 10.1016/j.nucmedbio.2011.04.006
– ident: e_1_2_7_74_1
  doi: 10.1016/j.jfluchem.2015.09.012
– ident: e_1_2_7_91_1
  doi: 10.1371/journal.pone.0059187
– start-page: 285
  volume-title: Radiopharm. Chem.
  year: 2019
  ident: e_1_2_7_29_1
  doi: 10.1007/978-3-319-98947-1_16
  contributor:
    fullname: Wagner M.
– ident: e_1_2_7_77_1
  doi: 10.1038/s41598-018-37186-2
– start-page: 273
  volume-title: Radiopharm. Chem.
  year: 2019
  ident: e_1_2_7_46_1
  doi: 10.1007/978-3-319-98947-1_15
  contributor:
    fullname: Ermert J.
– ident: e_1_2_7_88_1
  doi: 10.1039/C9CC02779C
– ident: e_1_2_7_3_1
  doi: 10.1053/snuc.2000.7439
SSID ssj0044818
Score 2.3430922
SecondaryResourceType review_article
Snippet Aliphatic fluorine-18 radiolabeling is the most commonly used method to synthesize tracers for PET-imaging. With an increasing demand for F-radiotracers for...
Aliphatic fluorine‐18 radiolabeling is the most commonly used method to synthesize tracers for PET‐imaging. With an increasing demand for 18 F‐radiotracers for...
SourceID proquest
crossref
pubmed
SourceType Aggregation Database
Index Database
StartPage 2612
SubjectTerms Fluorine Radioisotopes
Halogenation
Humans
Molecular Conformation
Positron-Emission Tomography
Radiopharmaceuticals - chemical synthesis
Radiopharmaceuticals - chemistry
Title Aliphatic 18 F-Radiofluorination: Recent Advances in the Labeling of Base-Sensitive Substrates
URI https://www.ncbi.nlm.nih.gov/pubmed/34169672
https://search.proquest.com/docview/2545594959
Volume 16
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1bb9MwFLZgSGgviDsdFxkJjQcWSJ3YSXgrl6kChqatk_ZElPjCIqVJtaRI49dzbMdJCpsEvKRVkqZVvq_H58Sfv4PQiyzxBclJ6CW6Ngk5Ix4MgsqjQkEqB7VYYtz1D76y-Un46ZSeDj1bzeqSNn_Nf166ruR_UIV9gKteJfsPyPYXhR3wHvCFLSAM27_CeFYWqzNjuTqNX-17R5koalWutaauF21AXqin-2d2rr9xusYvWW5XokOy-A5GMu9YK9mNjkjHEuNZ24wzV-0scCCFfhnNw7ettNacn8usz86Pz7Ly-7qqfxgRbQm_aln0GuC57DSJptN4kTVagaNcw9Du-QOZGoFV515tY2bMfA-GuGgjqLIxeaJxiGRWN_1H7LZesHwptLMkVKIQfoLxiXDPVkuDJIy8LGG25c9vbtnu0HV0Q1sj6m4KH456QzGoRaexs-70yZvNL9tGN93HN7OUK0oPk4IsbqNbXe2AZ5YId9A1Wd1Fu4fWfPxiDy-GtXTNHt7Fh4Mt-cU99K1nC57G-BK2vMWWK9hxBRcVBq5gxxVcK7zJFTxw5T462f-4eD_3uu4aHoeiGv6SVHv5xRllIsglIYqEKmdJFCs_gDQuJCLPck4jLv0cippcJYFu6sx8HkGNLVTwAG1VdSUfIZz4nMSSwhmBCinlmWSUCxHq0SBmcTBBL93dTFfWRCW1dtkk1RCkPQQT9Nzd7BTinJ68yipZr5uUQKpPEyjnkwl6aFHor-VQ27nyyGO0PXD3Cdpqz9fyKWSTbf7MEOQXij9ysw
link.rule.ids 314,780,784,27924,27925
linkProvider Wiley-Blackwell
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Aliphatic+18+F-Radiofluorination%3A+Recent+Advances+in+the+Labeling+of+Base-Sensitive+Substrates&rft.jtitle=ChemMedChem&rft.au=Bratteby%2C+Klas&rft.au=Shalgunov%2C+Vladimir&rft.au=Herth%2C+Matthias+Manfred&rft.date=2021-09-06&rft.eissn=1860-7187&rft.volume=16&rft.issue=17&rft.spage=2612&rft_id=info:doi/10.1002%2Fcmdc.202100303&rft_id=info%3Apmid%2F34169672&rft.externalDocID=34169672
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1860-7179&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1860-7179&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1860-7179&client=summon