Recent Advances in the Application of Selectfluor as a “Fluorine‐free” Functional Reagent in Organic Synthesis

Selectfluor, [1‐chloromethyl‐4‐fluoro‐1,4‐diazoniabicyclo‐[2.2.2]octane bis(tetrafluoroborate)], is not only an important electrophilic fluorinating agent but also a facile and efficient “fluorine‐free” functional reagent in other organic reactions. In this Minireview, we will present a brief histor...

Full description

Saved in:
Bibliographic Details
Published in:Chemistry, an Asian journal Vol. 15; no. 6; pp. 729 - 741
Main Authors: Yang, Ke, Song, Mengjie, Ali, Ahmed I. M., Mudassir, Syed M., Ge, Haibo
Format: Journal Article
Language:English
Published: Germany Wiley Subscription Services, Inc 16-03-2020
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Abstract Selectfluor, [1‐chloromethyl‐4‐fluoro‐1,4‐diazoniabicyclo‐[2.2.2]octane bis(tetrafluoroborate)], is not only an important electrophilic fluorinating agent but also a facile and efficient “fluorine‐free” functional reagent in other organic reactions. In this Minireview, we will present a brief history of Selectfluor as a transition metal oxidant, fluorine cation and radical initiator in “fluorine‐free” functionalizations over the last five years. Selectfluor as a “fluorine‐free” functional reagent in the application of various organic reactions as a transition‐metal oxidant, fluorine cation and radical initiator.
AbstractList Abstract Selectfluor, [1‐chloromethyl‐4‐fluoro‐1,4‐diazoniabicyclo‐[2.2.2]octane bis(tetrafluoroborate)], is not only an important electrophilic fluorinating agent but also a facile and efficient “fluorine‐free” functional reagent in other organic reactions. In this Minireview, we will present a brief history of Selectfluor as a transition metal oxidant, fluorine cation and radical initiator in “fluorine‐free” functionalizations over the last five years.
Selectfluor, [1‐chloromethyl‐4‐fluoro‐1,4‐diazoniabicyclo‐[2.2.2]octane bis(tetrafluoroborate)], is not only an important electrophilic fluorinating agent but also a facile and efficient “fluorine‐free” functional reagent in other organic reactions. In this Minireview, we will present a brief history of Selectfluor as a transition metal oxidant, fluorine cation and radical initiator in “fluorine‐free” functionalizations over the last five years.
Selectfluor, [1‐chloromethyl‐4‐fluoro‐1,4‐diazoniabicyclo‐[2.2.2]octane bis(tetrafluoroborate)], is not only an important electrophilic fluorinating agent but also a facile and efficient “fluorine‐free” functional reagent in other organic reactions. In this Minireview, we will present a brief history of Selectfluor as a transition metal oxidant, fluorine cation and radical initiator in “fluorine‐free” functionalizations over the last five years. Selectfluor as a “fluorine‐free” functional reagent in the application of various organic reactions as a transition‐metal oxidant, fluorine cation and radical initiator.
Author Ge, Haibo
Mudassir, Syed M.
Yang, Ke
Ali, Ahmed I. M.
Song, Mengjie
Author_xml – sequence: 1
  givenname: Ke
  surname: Yang
  fullname: Yang, Ke
  email: keyang@cczu.edu.cn
  organization: Indiana University Purdue University Indianapolis
– sequence: 2
  givenname: Mengjie
  surname: Song
  fullname: Song, Mengjie
  organization: Changzhou University
– sequence: 3
  givenname: Ahmed I. M.
  surname: Ali
  fullname: Ali, Ahmed I. M.
  organization: Texas Tech University
– sequence: 4
  givenname: Syed M.
  surname: Mudassir
  fullname: Mudassir, Syed M.
  organization: Indiana University Purdue University Indianapolis
– sequence: 5
  givenname: Haibo
  orcidid: 0000-0001-6727-4602
  surname: Ge
  fullname: Ge, Haibo
  email: hage@ttu.edu, geh@iupui.edu
  organization: Texas Tech University
BackLink https://www.ncbi.nlm.nih.gov/pubmed/32068956$$D View this record in MEDLINE/PubMed
BookMark eNqFkctKLDEQhoMo3rcuJeDGzYyppK_LRs6oIAiOgrsmna5opCc9Jt1HZucj-AD6cj6JaUZHcGM2lYKvPqr4d8i6bS0ScgBsDIzxE-mNHHPGWXgAa2QbsgRGUQp366s_z7bIjvePjMWc5dkm2RKcJVkeJ9uku0aFtqNF_V9ahZ4aS7sHpMV83hglO9Na2mo6xQZVp5u-dVR6KunHy9tk6IzFj5dX7TCUdzrprRpGZEOvUd4P4uC7cvfSGkWnCxvU3vg9sqFl43H_q-6S28m_m9Pz0eXV2cVpcTlSURo2F7qSIqm0wLRSOWRKIhdKRJhwgFpjCqjTGuo4rdNYoajrSmqhQHEeAyQodsnx0jt37VOPvitnxitsGmmx7X3JRZxGUQY8D-jRL_Sx7V04JFARz_KM54wFaryklGu9d6jLuTMz6RYlsHLIoxzyKFd5hIHDL21fzbBe4d8BBCBfAs-mwcUfurKYXhQ_8k_9ppyl
CitedBy_id crossref_primary_10_1021_acscatal_1c03052
crossref_primary_10_1002_slct_202300958
crossref_primary_10_1055_a_1701_6700
crossref_primary_10_1002_ejoc_202000815
crossref_primary_10_1016_j_tetlet_2022_154318
crossref_primary_10_1002_ajoc_202100590
crossref_primary_10_3390_ijms21113964
crossref_primary_10_1021_acs_orglett_4c00833
crossref_primary_10_1039_D2QO00663D
crossref_primary_10_1021_acs_joc_3c01355
crossref_primary_10_1021_acs_orglett_3c01350
crossref_primary_10_1039_D1QO01273H
crossref_primary_10_1016_j_molstruc_2023_137422
crossref_primary_10_1002_anie_202317070
crossref_primary_10_1016_j_tetlet_2021_153184
crossref_primary_10_1021_acs_orglett_1c01441
crossref_primary_10_1039_D2CC05569D
crossref_primary_10_1021_acscatal_3c03487
crossref_primary_10_3762_bjoc_20_129
crossref_primary_10_1016_j_tet_2023_133518
crossref_primary_10_1039_D1GC00175B
crossref_primary_10_1021_acs_orglett_1c03461
crossref_primary_10_1002_ajoc_202200164
crossref_primary_10_1016_j_checat_2024_101009
crossref_primary_10_1021_jacs_3c11042
crossref_primary_10_1039_D1QO00774B
crossref_primary_10_3390_molecules27051643
crossref_primary_10_59761_RCR5091
crossref_primary_10_1002_slct_202401194
crossref_primary_10_3389_fchem_2022_891858
crossref_primary_10_1002_ejoc_202400147
crossref_primary_10_1016_j_cclet_2021_12_073
crossref_primary_10_1002_slct_202300377
crossref_primary_10_1007_s10562_024_04665_3
crossref_primary_10_1021_acs_oprd_1c00375
crossref_primary_10_1039_D1OB02043A
crossref_primary_10_1039_D3OB00499F
crossref_primary_10_2174_0115701794268766231108110816
crossref_primary_10_1016_j_cclet_2024_109866
crossref_primary_10_1016_j_cclet_2020_11_036
crossref_primary_10_1016_j_tetlet_2022_154179
crossref_primary_10_1039_D2SC05735B
crossref_primary_10_1039_D0SC05137C
crossref_primary_10_1039_D3CC00377A
crossref_primary_10_1021_acs_orglett_2c02627
crossref_primary_10_1039_D2OB00519K
crossref_primary_10_1002_slct_202101925
crossref_primary_10_1002_ajoc_202400041
crossref_primary_10_1039_D3CC04728H
crossref_primary_10_1007_s41061_023_00437_6
crossref_primary_10_1055_a_1899_5563
crossref_primary_10_1002_slct_202204773
crossref_primary_10_1002_ange_202317070
Cites_doi 10.1021/acs.joc.9b00965
10.1016/j.tet.2016.11.069
10.6023/cjoc201904058
10.1002/slct.201900113
10.1039/C5CS00272A
10.1039/C7OB00913E
10.1021/acs.joc.5b00857
10.1039/C9CC04287C
10.1021/acs.orglett.9b00067
10.1002/ange.200400648
10.1039/C9RA01481K
10.1002/anie.201609105
10.1021/jacs.8b03704
10.1016/j.tet.2019.130533
10.1126/science.aam9041
10.1021/ol500670h
10.1021/acs.orglett.9b01635
10.3390/molecules23102673
10.3390/molecules16086432
10.6023/cjoc201801036
10.1021/acs.joc.5b02593
10.1039/C9OB00972H
10.1021/acs.orglett.8b02422
10.2174/1568026614666140202205531
10.1055/s-0037-1610005
10.1002/cssc.201900151
10.1021/acs.joc.9b02202
10.1002/chir.23039
10.1002/chem.201804229
10.1055/s-0036-1588536
10.1039/C8RA01796D
10.1002/slct.201801996
10.1021/jacs.8b13534
10.1021/acs.joc.6b02212
10.1021/ja1034123
10.1002/slct.201802450
10.1039/C7GC03106H
10.1038/s41467-019-08413-9
10.1039/C9QO01073D
10.1039/C5QO00004A
10.1021/acscatal.7b03841
10.1002/anie.200900585
10.1002/ejoc.201501186
10.1021/acs.orglett.6b01250
10.1002/ejoc.201900960
10.1039/C8OB01348A
10.1039/C6RA22653A
10.1016/j.tet.2018.05.061
10.1021/cr500277b
10.1002/ejoc.201600982
10.6023/cjoc201701054
10.1039/C8OB02348D
10.1016/j.bmcl.2017.01.027
10.1021/acs.chemrev.6b00567
10.1021/ja909555d
10.1039/C7OB01723E
10.1002/ejoc.201901092
10.1111/cod.12391
10.1021/cr500366b
10.1021/acs.joc.6b01932
10.1139/cjc-2018-0181
10.1002/ejoc.201801090
10.1016/j.jphotochem.2017.09.075
10.1002/ange.200900585
10.1021/acscatal.6b00293
10.1021/acs.orglett.7b02706
10.1021/acs.orglett.5b00376
10.1021/jo502823m
10.1055/s-0036-1588693
10.1002/anie.200400648
10.1021/acs.chemrev.5b00360
10.1039/C9QO00845D
10.1021/acs.joc.7b01790
10.1021/acs.joc.9b01004
10.1039/C6CS00107F
10.1021/acs.jmedchem.6b01280
10.1002/ange.201609105
10.1021/cr500706a
10.1016/j.chempr.2018.02.001
10.1021/acs.orglett.5b02522
10.1002/ejoc.201500610
10.1021/acs.orglett.9b00744
10.1021/acs.joc.7b00190
ContentType Journal Article
Copyright 2020 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim
2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
Copyright_xml – notice: 2020 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim
– notice: 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
DBID NPM
AAYXX
CITATION
K9.
7X8
DOI 10.1002/asia.202000011
DatabaseName PubMed
CrossRef
ProQuest Health & Medical Complete (Alumni)
MEDLINE - Academic
DatabaseTitle PubMed
CrossRef
ProQuest Health & Medical Complete (Alumni)
MEDLINE - Academic
DatabaseTitleList CrossRef
ProQuest Health & Medical Complete (Alumni)
PubMed

DeliveryMethod fulltext_linktorsrc
Discipline Chemistry
EISSN 1861-471X
EndPage 741
ExternalDocumentID 10_1002_asia_202000011
32068956
ASIA202000011
Genre reviewArticle
Journal Article
Review
GrantInformation_xml – fundername: Indiana University Purdue University Indianapolis
– fundername: Texas Tech University
– fundername: NSF
  funderid: CHE-1350541; 1855735
– fundername: NSFC
  funderid: 21702019
– fundername: Advanced Catalysis and Green Manufacturing Collaborative Innovation Center, Changzhou University
– fundername: NSFC
  grantid: 21702019
– fundername: NSF
  grantid: CHE-1350541
– fundername: NSF
  grantid: 1855735
GroupedDBID ---
05W
0R~
1L6
1OC
29B
33P
3WU
4.4
5GY
6J9
8-1
87K
8UM
A00
AAESR
AAIHA
AANLZ
AASGY
AAXRX
AAZKR
ABCUV
ABDBF
ABIJN
ABJNI
ACAHQ
ACCZN
ACGFS
ACIWK
ACPOU
ACXBN
ACXQS
ADBBV
ADKYN
ADMGS
ADOZA
ADXAS
ADZMN
AEGXH
AEIGN
AEUQT
AEUYR
AFBPY
AFFPM
AFGKR
AHBTC
AHMBA
AITYG
AIURR
ALMA_UNASSIGNED_HOLDINGS
AMYDB
AZVAB
BDRZF
BFHJK
BMXJE
BRXPI
CS3
DCZOG
DRFUL
DRSTM
EBD
EBS
F5P
G-S
HBH
HGLYW
HHY
HHZ
HZ~
LATKE
LAW
LEEKS
LITHE
LOXES
LUTES
LYRES
MEWTI
MXFUL
MXSTM
MY~
O66
O9-
OIG
P2W
P4E
PQQKQ
QRW
RAD
ROL
RWI
SUPJJ
WBKPD
WHG
WOHZO
WXSBR
WYJ
XSW
XV2
ZZTAW
~S-
NPM
AAYXX
CITATION
K9.
7X8
ID FETCH-LOGICAL-c4761-3fba36bf3e7bc918cae23c34e6211dfe71ef7d1d57d75ce3ddbaf3c1c225116e3
IEDL.DBID 33P
ISSN 1861-4728
IngestDate Thu Oct 24 23:57:52 EDT 2024
Thu Oct 10 18:03:02 EDT 2024
Thu Sep 12 19:21:07 EDT 2024
Sat Sep 28 08:29:56 EDT 2024
Sat Aug 24 01:41:09 EDT 2024
IsPeerReviewed true
IsScholarly true
Issue 6
Keywords “fluorine-free” functional reagent
electrophilic fluorinating reagent
organic synthesis
Selectfluor
Language English
License 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c4761-3fba36bf3e7bc918cae23c34e6211dfe71ef7d1d57d75ce3ddbaf3c1c225116e3
Notes ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-3
content type line 23
ObjectType-Review-1
ORCID 0000-0001-6727-4602
PMID 32068956
PQID 2428982900
PQPubID 986338
PageCount 13
ParticipantIDs proquest_miscellaneous_2357448129
proquest_journals_2428982900
crossref_primary_10_1002_asia_202000011
pubmed_primary_32068956
wiley_primary_10_1002_asia_202000011_ASIA202000011
PublicationCentury 2000
PublicationDate March 16, 2020
PublicationDateYYYYMMDD 2020-03-16
PublicationDate_xml – month: 03
  year: 2020
  text: March 16, 2020
  day: 16
PublicationDecade 2020
PublicationPlace Germany
PublicationPlace_xml – name: Germany
– name: Weinheim
PublicationTitle Chemistry, an Asian journal
PublicationTitleAlternate Chem Asian J
PublicationYear 2020
Publisher Wiley Subscription Services, Inc
Publisher_xml – name: Wiley Subscription Services, Inc
References 2019; 2019
2017; 82
2019; 97
2009 2009; 48 121
2015; 73
2019; 55
2017; 49
2019; 10
2019; 12
2019; 17
2016; 2016
2015; 80
2011; 16
2017; 356
2017; 117
2017; 73
2018; 8
2018; 3
2018; 4
2017; 37
2019; 21
2015; 44
2014; 16
2014; 14
2005 2005; 44 117
2018; 74
2016; 116
2016; 81
2018; 38
2016; 45
2015; 2
2019; 9
2015; 17
2019; 4
2019; 6
2018; 140
2019; 75
2019; 31
2017; 28
2017; 27
2019; 39
2006; 2
2017 2017; 56 129
2018; 23
2016; 18
2019; 141
2018; 20
2016; 59
2018; 24
2016; 6
2018; 2018
2019; 84
2015; 115
2017; 15
2018; 355
2010; 132
2015; 2015
2005; 52
2017; 19
2018; 50
2018; 16
e_1_2_8_28_2
e_1_2_8_47_1
e_1_2_8_24_2
e_1_2_8_45_2
e_1_2_8_24_3
e_1_2_8_49_1
e_1_2_8_26_2
e_1_2_8_68_2
e_1_2_8_81_1
e_1_2_8_3_2
e_1_2_8_5_2
e_1_2_8_7_3
e_1_2_8_9_1
Stavber S. (e_1_2_8_6_2) 2006; 2
e_1_2_8_7_2
e_1_2_8_20_1
e_1_2_8_66_1
e_1_2_8_89_1
e_1_2_8_41_2
e_1_2_8_22_1
e_1_2_8_87_1
e_1_2_8_43_2
e_1_2_8_64_2
e_1_2_8_85_1
e_1_2_8_62_2
e_1_2_8_1_1
e_1_2_8_60_1
e_1_2_8_83_1
e_1_2_8_17_2
e_1_2_8_19_1
e_1_2_8_19_2
e_1_2_8_36_1
e_1_2_8_59_1
e_1_2_8_13_2
e_1_2_8_34_2
e_1_2_8_15_1
e_1_2_8_38_1
e_1_2_8_57_1
e_1_2_8_55_1
e_1_2_8_78_1
e_1_2_8_30_2
e_1_2_8_11_1
e_1_2_8_53_1
e_1_2_8_76_1
e_1_2_8_32_2
e_1_2_8_51_1
e_1_2_8_74_1
e_1_2_8_72_2
e_1_2_8_70_2
e_1_2_8_27_2
e_1_2_8_29_2
e_1_2_8_23_2
e_1_2_8_69_2
e_1_2_8_46_1
e_1_2_8_25_2
e_1_2_8_67_2
e_1_2_8_48_1
e_1_2_8_2_2
e_1_2_8_80_1
e_1_2_8_4_2
e_1_2_8_42_2
e_1_2_8_21_1
e_1_2_8_88_1
e_1_2_8_44_2
e_1_2_8_63_2
e_1_2_8_65_1
e_1_2_8_86_1
e_1_2_8_84_1
e_1_2_8_40_2
e_1_2_8_61_1
e_1_2_8_82_1
e_1_2_8_39_1
e_1_2_8_18_2
e_1_2_8_12_2
e_1_2_8_35_1
e_1_2_8_14_2
e_1_2_8_16_1
e_1_2_8_37_1
e_1_2_8_58_1
e_1_2_8_79_1
Stavber S. (e_1_2_8_8_1) 2005; 52
e_1_2_8_31_2
e_1_2_8_10_1
e_1_2_8_56_1
e_1_2_8_77_1
e_1_2_8_33_2
e_1_2_8_54_1
e_1_2_8_75_1
e_1_2_8_73_2
e_1_2_8_52_1
e_1_2_8_71_2
e_1_2_8_50_1
References_xml – volume: 4
  start-page: 1208
  year: 2018
  end-page: 1262
  publication-title: Chem
– volume: 21
  start-page: 2518
  year: 2019
  end-page: 2522
  publication-title: Org. Lett.
– volume: 82
  start-page: 3702
  year: 2017
  end-page: 3709
  publication-title: J. Org. Chem.
– volume: 17
  start-page: 1489
  year: 2015
  end-page: 1492
  publication-title: Org. Lett.
– volume: 6
  start-page: 3996
  year: 2019
  end-page: 3999
  publication-title: Org. Chem. Front.
– volume: 2015
  start-page: 5381
  year: 2015
  end-page: 5388
  publication-title: Eur. J. Org. Chem.
– volume: 4
  start-page: 2404
  year: 2019
  end-page: 2408
  publication-title: ChemistrySelect
– volume: 20
  start-page: 760
  year: 2018
  end-page: 764
  publication-title: Green Chem.
– volume: 24
  start-page: 16895
  year: 2018
  end-page: 16901
  publication-title: Chem. Eur. J.
– volume: 82
  start-page: 12059
  year: 2017
  end-page: 12065
  publication-title: J. Org. Chem.
– volume: 73
  start-page: 154
  year: 2017
  end-page: 163
  publication-title: Tetrahedron
– volume: 73
  start-page: 60
  year: 2015
  end-page: 62
  publication-title: Contact Dermatitis.
– volume: 356
  start-page: 1059
  year: 2017
  end-page: 1063
  publication-title: Science
– volume: 16
  start-page: 6017
  year: 2018
  end-page: 6024
  publication-title: Org. Biomol. Chem.
– volume: 2019
  start-page: 5812
  year: 2019
  end-page: 5814
  publication-title: Eur. J. Org. Chem.
– volume: 50
  start-page: 2915
  year: 2018
  end-page: 2923
  publication-title: Synthesis
– volume: 17
  start-page: 6342
  year: 2019
  end-page: 6345
  publication-title: Org. Biomol. Chem.
– volume: 117
  start-page: 8787
  year: 2017
  end-page: 8863
  publication-title: Chem. Rev.
– volume: 45
  start-page: 4590
  year: 2016
  end-page: 4627
  publication-title: Chem. Soc. Rev.
– volume: 28
  start-page: 640
  year: 2017
  end-page: 653
  publication-title: Synlett
– volume: 55
  start-page: 9689
  year: 2019
  end-page: 9692
  publication-title: Chem. Commun.
– volume: 16
  start-page: 2602
  year: 2014
  end-page: 2605
  publication-title: Org. Lett.
– volume: 37
  start-page: 1290
  year: 2017
  end-page: 1294
  publication-title: Chin. J. Org. Chem.
– volume: 2016
  start-page: 5545
  year: 2016
  end-page: 5558
  publication-title: Eur. J. Org. Chem.
– volume: 3
  start-page: 9374
  year: 2018
  end-page: 9377
  publication-title: ChemistrySelect
– volume: 23
  start-page: 2673
  year: 2018
  end-page: 2688
  publication-title: Molecules
– volume: 17
  start-page: 5048
  year: 2015
  end-page: 5051
  publication-title: Org. Lett.
– volume: 59
  start-page: 9906
  year: 2016
  end-page: 9918
  publication-title: J. Med. Chem.
– volume: 115
  start-page: 9073
  year: 2015
  end-page: 9174
  publication-title: Chem. Rev.
– volume: 38
  start-page: 1712
  year: 2018
  end-page: 1717
  publication-title: Chin. J. Org. Chem.
– volume: 132
  start-page: 1474
  year: 2010
  end-page: 1475
  publication-title: J. Am. Chem. Soc.
– volume: 132
  start-page: 8885
  year: 2010
  end-page: 8887
  publication-title: J. Am. Chem. Soc.
– volume: 141
  start-page: 1918
  year: 2019
  end-page: 1922
  publication-title: J. Am. Chem. Soc.
– volume: 84
  start-page: 14045
  year: 2019
  publication-title: J. Org. Chem.
– volume: 18
  start-page: 2758
  year: 2016
  end-page: 2761
  publication-title: Org. Lett.
– volume: 75
  start-page: 130533
  year: 2019
  end-page: 130540
  publication-title: Tetrahedron
– volume: 48 121
  start-page: 3112 3158
  year: 2009 2009
  end-page: 3115 3161
  publication-title: Angew. Chem. Int. Ed. Angew. Chem.
– volume: 44 117
  start-page: 192 196
  year: 2005 2005
  end-page: 212 217
  publication-title: Angew. Chem. Int. Ed. Angew. Chem.
– volume: 49
  start-page: 4586
  year: 2017
  end-page: 4598
  publication-title: Synthesis
– volume: 97
  start-page: 37
  year: 2019
  end-page: 41
  publication-title: Can. J. Chem.
– volume: 16
  start-page: 8884
  year: 2018
  end-page: 8898
  publication-title: Org. Biomol. Chem.
– volume: 20
  start-page: 6046
  year: 2018
  end-page: 6050
  publication-title: Org. Lett.
– volume: 80
  start-page: 6856
  year: 2015
  end-page: 6863
  publication-title: J. Org. Chem.
– volume: 2
  start-page: 213
  year: 2006
  end-page: 268
  publication-title: Adv. Org. Synth.
– volume: 6
  start-page: 2341
  year: 2016
  end-page: 2351
  publication-title: ACS Catal.
– volume: 21
  start-page: 6179
  year: 2019
  end-page: 6184
  publication-title: Org. Lett.
– volume: 84
  start-page: 9044
  year: 2019
  end-page: 9050
  publication-title: J. Org. Chem.
– volume: 115
  start-page: 612
  year: 2015
  end-page: 633
  publication-title: Chem. Rev.
– volume: 8
  start-page: 579
  year: 2018
  end-page: 583
  publication-title: ACS Catal.
– volume: 52
  start-page: 13
  year: 2005
  end-page: 26
  publication-title: Acta Chim. Slov.
– volume: 81
  start-page: 1476
  year: 2016
  end-page: 1483
  publication-title: J. Org. Chem.
– volume: 19
  start-page: 5772
  year: 2017
  end-page: 5775
  publication-title: Org. Lett.
– volume: 74
  start-page: 3879
  year: 2018
  end-page: 3887
  publication-title: Tetrahedron
– volume: 21
  start-page: 2441
  year: 2019
  end-page: 2444
  publication-title: Org. Lett.
– volume: 12
  start-page: 2955
  year: 2019
  end-page: 2969
  publication-title: ChemSusChem
– volume: 31
  start-page: 91
  year: 2019
  end-page: 96
  publication-title: Chirality
– volume: 2015
  start-page: 7859
  year: 2015
  end-page: 7868
  publication-title: Eur. J. Org. Chem.
– volume: 56 129
  start-page: 49 49
  year: 2017 2017
  end-page: 51 51
  publication-title: Angew. Chem. Int. Ed. Angew. Chem.
– volume: 140
  start-page: 8069
  year: 2018
  end-page: 8073
  publication-title: J. Am. Chem. Soc.
– volume: 6
  start-page: 3644
  year: 2019
  end-page: 3648
  publication-title: Org. Chem. Front.
– volume: 27
  start-page: 1291
  year: 2017
  end-page: 1295
  publication-title: Bioorg. Med. Chem. Lett.
– volume: 355
  start-page: 120
  year: 2018
  end-page: 124
  publication-title: J. Photochem. Photobiol. A
– volume: 44
  start-page: 7764
  year: 2015
  end-page: 7786
  publication-title: Chem. Soc. Rev.
– volume: 2
  start-page: 1107
  year: 2015
  end-page: 1295
  publication-title: Org. Chem. Front.
– volume: 80
  start-page: 2842
  year: 2015
  end-page: 2847
  publication-title: J. Org. Chem.
– volume: 2019
  start-page: 5998
  year: 2019
  end-page: 6002
  publication-title: Eur. J. Org. Chem.
– volume: 10
  start-page: 467
  year: 2019
  end-page: 473
  publication-title: Nat. Commun.
– volume: 6
  start-page: 93486
  year: 2016
  end-page: 93490
  publication-title: RSC Adv.
– volume: 82
  start-page: 109
  year: 2017
  end-page: 118
  publication-title: J. Org. Chem.
– volume: 15
  start-page: 4432
  year: 2017
  end-page: 4439
  publication-title: Org. Biomol. Chem.
– volume: 14
  start-page: 901
  year: 2014
  end-page: 940
  publication-title: Curr. Top. Med. Chem.
– volume: 8
  start-page: 13671
  year: 2018
  end-page: 13674
  publication-title: RSC Adv.
– volume: 3
  start-page: 13006
  year: 2018
  end-page: 13009
  publication-title: ChemistrySelect
– volume: 16
  start-page: 6432
  year: 2011
  end-page: 6464
  publication-title: Molecules
– volume: 81
  start-page: 10043
  year: 2016
  end-page: 10048
  publication-title: J. Org. Chem.
– volume: 15
  start-page: 7140
  year: 2017
  end-page: 7146
  publication-title: Org. Biomol. Chem.
– volume: 84
  start-page: 12131
  year: 2019
  end-page: 12137
  publication-title: J. Org. Chem.
– volume: 39
  start-page: 2821
  year: 2019
  end-page: 2828
  publication-title: Chin. J. Org. Chem.
– volume: 9
  start-page: 10340
  year: 2019
  end-page: 10344
  publication-title: RSC Adv.
– volume: 116
  start-page: 287
  year: 2016
  end-page: 322
  publication-title: Chem. Rev.
– volume: 2018
  start-page: 5520
  year: 2018
  end-page: 5523
  publication-title: Eur. J. Org. Chem.
– volume: 115
  start-page: 826
  year: 2015
  end-page: 870
  publication-title: Chem. Rev.
– ident: e_1_2_8_83_1
  doi: 10.1021/acs.joc.9b00965
– ident: e_1_2_8_43_2
  doi: 10.1016/j.tet.2016.11.069
– ident: e_1_2_8_45_2
  doi: 10.6023/cjoc201904058
– ident: e_1_2_8_60_1
  doi: 10.1002/slct.201900113
– ident: e_1_2_8_29_2
  doi: 10.1039/C5CS00272A
– ident: e_1_2_8_22_1
– ident: e_1_2_8_71_2
  doi: 10.1039/C7OB00913E
– ident: e_1_2_8_75_1
  doi: 10.1021/acs.joc.5b00857
– ident: e_1_2_8_86_1
  doi: 10.1039/C9CC04287C
– ident: e_1_2_8_68_2
  doi: 10.1021/acs.orglett.9b00067
– ident: e_1_2_8_7_3
  doi: 10.1002/ange.200400648
– ident: e_1_2_8_58_1
  doi: 10.1039/C9RA01481K
– ident: e_1_2_8_24_2
  doi: 10.1002/anie.201609105
– ident: e_1_2_8_47_1
  doi: 10.1021/jacs.8b03704
– ident: e_1_2_8_44_2
  doi: 10.1016/j.tet.2019.130533
– ident: e_1_2_8_70_2
  doi: 10.1126/science.aam9041
– ident: e_1_2_8_34_2
  doi: 10.1021/ol500670h
– ident: e_1_2_8_89_1
  doi: 10.1021/acs.orglett.9b01635
– ident: e_1_2_8_12_2
  doi: 10.3390/molecules23102673
– ident: e_1_2_8_9_1
  doi: 10.3390/molecules16086432
– ident: e_1_2_8_76_1
  doi: 10.6023/cjoc201801036
– ident: e_1_2_8_55_1
  doi: 10.1021/acs.joc.5b02593
– ident: e_1_2_8_82_1
  doi: 10.1039/C9OB00972H
– ident: e_1_2_8_51_1
  doi: 10.1021/acs.orglett.8b02422
– ident: e_1_2_8_66_1
– ident: e_1_2_8_5_2
  doi: 10.2174/1568026614666140202205531
– ident: e_1_2_8_36_1
  doi: 10.1055/s-0037-1610005
– ident: e_1_2_8_23_2
  doi: 10.1002/cssc.201900151
– ident: e_1_2_8_38_1
  doi: 10.1021/acs.joc.9b02202
– ident: e_1_2_8_77_1
  doi: 10.1002/chir.23039
– ident: e_1_2_8_85_1
  doi: 10.1002/chem.201804229
– volume: 52
  start-page: 13
  year: 2005
  ident: e_1_2_8_8_1
  publication-title: Acta Chim. Slov.
  contributor:
    fullname: Stavber S.
– ident: e_1_2_8_15_1
  doi: 10.1055/s-0036-1588536
– volume: 2
  start-page: 213
  year: 2006
  ident: e_1_2_8_6_2
  publication-title: Adv. Org. Synth.
  contributor:
    fullname: Stavber S.
– ident: e_1_2_8_32_2
  doi: 10.1039/C8RA01796D
– ident: e_1_2_8_57_1
  doi: 10.1002/slct.201801996
– ident: e_1_2_8_67_2
  doi: 10.1021/jacs.8b13534
– ident: e_1_2_8_42_2
  doi: 10.1021/acs.joc.6b02212
– ident: e_1_2_8_61_1
– ident: e_1_2_8_18_2
  doi: 10.1021/ja1034123
– ident: e_1_2_8_56_1
  doi: 10.1002/slct.201802450
– ident: e_1_2_8_81_1
  doi: 10.1039/C7GC03106H
– ident: e_1_2_8_87_1
  doi: 10.1038/s41467-019-08413-9
– ident: e_1_2_8_31_2
  doi: 10.1039/C9QO01073D
– ident: e_1_2_8_30_2
  doi: 10.1039/C5QO00004A
– ident: e_1_2_8_69_2
  doi: 10.1021/acscatal.7b03841
– ident: e_1_2_8_19_1
  doi: 10.1002/anie.200900585
– ident: e_1_2_8_28_2
  doi: 10.1002/ejoc.201501186
– ident: e_1_2_8_72_2
  doi: 10.1021/acs.orglett.6b01250
– ident: e_1_2_8_74_1
  doi: 10.1002/ejoc.201900960
– ident: e_1_2_8_80_1
  doi: 10.1039/C8OB01348A
– ident: e_1_2_8_79_1
  doi: 10.1039/C6RA22653A
– ident: e_1_2_8_50_1
  doi: 10.1016/j.tet.2018.05.061
– ident: e_1_2_8_4_2
  doi: 10.1021/cr500277b
– ident: e_1_2_8_41_2
  doi: 10.1002/ejoc.201600982
– ident: e_1_2_8_11_1
– ident: e_1_2_8_46_1
  doi: 10.6023/cjoc201701054
– ident: e_1_2_8_13_2
  doi: 10.1039/C8OB02348D
– ident: e_1_2_8_62_2
  doi: 10.1016/j.bmcl.2017.01.027
– ident: e_1_2_8_25_2
  doi: 10.1021/acs.chemrev.6b00567
– ident: e_1_2_8_39_1
– ident: e_1_2_8_17_2
  doi: 10.1021/ja909555d
– ident: e_1_2_8_33_2
  doi: 10.1039/C7OB01723E
– ident: e_1_2_8_53_1
  doi: 10.1002/ejoc.201901092
– ident: e_1_2_8_64_2
  doi: 10.1111/cod.12391
– ident: e_1_2_8_2_2
  doi: 10.1021/cr500366b
– ident: e_1_2_8_1_1
– ident: e_1_2_8_52_1
  doi: 10.1021/acs.joc.6b01932
– ident: e_1_2_8_59_1
  doi: 10.1139/cjc-2018-0181
– ident: e_1_2_8_65_1
  doi: 10.1002/ejoc.201801090
– ident: e_1_2_8_84_1
  doi: 10.1016/j.jphotochem.2017.09.075
– ident: e_1_2_8_19_2
  doi: 10.1002/ange.200900585
– ident: e_1_2_8_27_2
  doi: 10.1021/acscatal.6b00293
– ident: e_1_2_8_35_1
  doi: 10.1021/acs.orglett.7b02706
– ident: e_1_2_8_49_1
  doi: 10.1021/acs.orglett.5b00376
– ident: e_1_2_8_48_1
  doi: 10.1021/jo502823m
– ident: e_1_2_8_16_1
– ident: e_1_2_8_10_1
  doi: 10.1055/s-0036-1588693
– ident: e_1_2_8_7_2
  doi: 10.1002/anie.200400648
– ident: e_1_2_8_73_2
  doi: 10.1021/acs.chemrev.5b00360
– ident: e_1_2_8_78_1
  doi: 10.1039/C9QO00845D
– ident: e_1_2_8_54_1
  doi: 10.1021/acs.joc.7b01790
– ident: e_1_2_8_37_1
  doi: 10.1021/acs.joc.9b01004
– ident: e_1_2_8_26_2
  doi: 10.1039/C6CS00107F
– ident: e_1_2_8_63_2
  doi: 10.1021/acs.jmedchem.6b01280
– ident: e_1_2_8_24_3
  doi: 10.1002/ange.201609105
– ident: e_1_2_8_3_2
  doi: 10.1021/cr500706a
– ident: e_1_2_8_14_2
  doi: 10.1016/j.chempr.2018.02.001
– ident: e_1_2_8_20_1
  doi: 10.1021/acs.orglett.5b02522
– ident: e_1_2_8_40_2
  doi: 10.1002/ejoc.201500610
– ident: e_1_2_8_88_1
  doi: 10.1021/acs.orglett.9b00744
– ident: e_1_2_8_21_1
  doi: 10.1021/acs.joc.7b00190
SSID ssj0052098
Score 2.5383766
SecondaryResourceType review_article
Snippet Selectfluor, [1‐chloromethyl‐4‐fluoro‐1,4‐diazoniabicyclo‐[2.2.2]octane bis(tetrafluoroborate)], is not only an important electrophilic fluorinating agent but...
Selectfluor, [1-chloromethyl-4-fluoro-1,4-diazoniabicyclo-[2.2.2]octane bis(tetrafluoroborate)], is not only an important electrophilic fluorinating agent but...
Abstract Selectfluor, [1‐chloromethyl‐4‐fluoro‐1,4‐diazoniabicyclo‐[2.2.2]octane bis(tetrafluoroborate)], is not only an important electrophilic fluorinating...
SourceID proquest
crossref
pubmed
wiley
SourceType Aggregation Database
Index Database
Publisher
StartPage 729
SubjectTerms Chemical reactions
Chemistry
electrophilic fluorinating reagent
Fluorine
organic synthesis
Oxidizing agents
Reagents
Selectfluor
Transition metals
“fluorine-free” functional reagent
Title Recent Advances in the Application of Selectfluor as a “Fluorine‐free” Functional Reagent in Organic Synthesis
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fasia.202000011
https://www.ncbi.nlm.nih.gov/pubmed/32068956
https://www.proquest.com/docview/2428982900
https://search.proquest.com/docview/2357448129
Volume 15
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV3NTtwwELboXuBSKL_b0spISJwiEntjO8doYUUvFWJbiVvk2GMJCWXRZvfAjUfgAejL8SSdSTZBqx6Q2lMSJXYsj-35ZsbzmbFTmXqjstREXgsZjUaijKylXBlpvZagYmh4C66m-setubgkmpw-i7_lh-gdbjQzmvWaJrgt6_M30lBKMkT7TjT-abJ_iLqJcjjkdbcU0xaPJhfOKDSUtDAda2MszteLr2ulv6DmOnJtVM9k-_8bvcM-rmAnz9tx8oltQLXLNsfdaW97bIH4EfUPz9s9ATW_qzhiQ56_Bbj5LPBpc2xOuF_O5tzW3PLXp5cJPWHLXp-ewxzw8ptPUFu2TkZ-A5ayt6i-Nu_T8eljhVXXd_U--zW5_Dm-ilYnMkRupMlRFUorVRkk6NJliXEWhHRyBArtSB9AJxC0T3yqvU4dSO9LG6RLnCBLRoE8YINqVsER4yUBERdcnFFMGVwGIiiLBhKYtJQyHrKzTiLFQ0u8UbQUy6KgXiz6Xhyy405gxWoC1gUiD5NRkBgrOulfY59SPMRWMFviNzLVaJ0i4hmyw1bQ_a-kiJVB23HIRCPPd9pQ5NPvef_0-V8KfWFbdE_72xJ1zAaL-RK-sg-1X35rBvUfzwH4KA
link.rule.ids 315,783,787,1409,27936,27937,46067,46491
linkProvider Wiley-Blackwell
linkToHtml http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV3NatwwEBZpckgvadK_bJsfFQo9mdiSLclHk2bZkDSUbgq9GVkaQaB4wzp7yC2P0AdoXy5P0hl77bD0ECg5GdmWLDQa6_tmNCPGPsrMG5VnJvJayChNRRVZS7Ey0notQcXQ5i2YTPXFD_P5hNLkFH0sTJcfYjC4kWa0_2tScDJIHz1kDaUoQyR4ojVQIwHaSFWak25K-bX_GdMmjzYaziikSlqYPm9jLI5W66-uS_-AzVXs2i4-4xdP0O1ttrVEnrzopsoOW4P6Jds87g98e8VuEELiEsSLbltAw69qjvCQFw8-bj4LfNqenBN-LmZzbhtu-f3d7zGVsGv3d7_CHPDyh49xwezsjPwbWArgova60E_Hp7c1Nt1cNa_Z9_HJ5fEkWh7KELlUk60qVFaqKkjQlcsT4ywI6WQKCqmkD6ATCNonPtNeZw6k95UN0iVOEJlRIN-w9XpWwy7jFWERF1yck1sZXA4iKIscCUxWSRmP2KdeJOV1l3uj7LIsi5JGsRxGccT2eomVSx1sSgQfJic_MTb0YXiMY0ouEVvDbIHvyEwjQUXQM2JvO0kPn5IiVgbp44iJVqCP9KEspqfFUHr3P5UO2ebk8st5eX56cfaePaf7tN0tUXts_Wa-gH32rPGLg3aG_wVosvxJ
linkToPdf http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV3BatwwEBVpCm0uTZu26TZpq0ChJxNbsiX5aJKYhJQQsin0ZmRpBIHiDevsobd8Qj-g_bl8SWfstcOSQ6A9GdmWLDSS570ZzYixzzLzRuWZibwWMkpTUUfWUqyMtF5LUDF0eQuOp_rsuzk8ojQ5YxR_nx9iNLjRyuj-17TAr33Yv08aSkGGyO9EZ59G_vM0RSxO9EvK8-FfTHs8umA4o5ApaWGGtI2x2F-tv6qWHmDNVeja6Z5y8_97_ZK9WOJOXvQT5RVbg2aLPT8Yjnt7zW4QQKIC4kW_KaDlVw1HcMiLew83nwU-7c7NCT8Wszm3Lbf87vZ3SSXs2d3trzAHvPzhJarL3srIL8BS-Ba11wd-Oj792WDT7VX7hn0rjy4PjqPlkQyRSzVZqkJtpaqDBF27PDHOgpBOpqCQSPoAOoGgfeIz7XXmQHpf2yBd4gRRGQXyLVtvZg28Y7wmJOKCi3NyKoPLQQRlkSGByWop4wn7Mkikuu4zb1R9jmVR0ShW4yhO2O4gsGq5AtsKoYfJyUuMDe2Nj3FMySFiG5gt8B2ZaaSnCHkmbLsX9PgpKWJlkDxOmOjk-UgfqmJ6Uoyl9_9S6RN7dn5YVl9Pzk532Abdpr1uidpl6zfzBXxgT1q_-NjN779y9Pr4
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=Recent+Advances+in+the+Application+of+Selectfluor+as+a+%E2%80%9CFluorine%E2%80%90free%E2%80%9D+Functional+Reagent+in+Organic+Synthesis&rft.jtitle=Chemistry%2C+an+Asian+journal&rft.au=Yang%2C+Ke&rft.au=Song%2C+Mengjie&rft.au=Ali%2C+Ahmed+I.+M.&rft.au=Mudassir%2C+Syed+M.&rft.date=2020-03-16&rft.issn=1861-4728&rft.eissn=1861-471X&rft.volume=15&rft.issue=6&rft.spage=729&rft.epage=741&rft_id=info:doi/10.1002%2Fasia.202000011&rft.externalDBID=10.1002%252Fasia.202000011&rft.externalDocID=ASIA202000011
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1861-4728&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1861-4728&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1861-4728&client=summon