Emergence of Copper‐Mediated Formation of C–C Bonds

Copper‐catalyzed cross‐coupling reactions have found widespread application in carbon–carbon or carbon–heteroatom bond formation. The relatively low toxicity, ease of handling, and low cost of these versatile complexes make them attractive for the elaboration of new methodologies and for the obtaini...

Full description

Saved in:
Bibliographic Details
Published inEuropean journal of organic chemistry Vol. 2017; no. 2; pp. 209 - 228
Main Authors Maaliki, Carine, Thiery, Emilie, Thibonnet, Jérôme
Format Journal Article
LanguageEnglish
Published Weinheim Wiley Subscription Services, Inc 10.01.2017
Wiley-VCH Verlag
Subjects
Carbon
Chemical Sciences
Copper
C–C coupling
Decarboxylative coupling
Dehydrogenative coupling
Domino reactions
Organic chemistry
Synthetic methods
C-C coupling
carbon carbon bond
liaison carbone carbone
décarboxylation
déhydrogenase
domini reactions
decarboxylative coupling
dehydrogenative coupling
Copper
synthetic methods
Online AccessGet full text

Cover

Abstract Copper‐catalyzed cross‐coupling reactions have found widespread application in carbon–carbon or carbon–heteroatom bond formation. The relatively low toxicity, ease of handling, and low cost of these versatile complexes make them attractive for the elaboration of new methodologies and for the obtaining of new compounds. We focus on recent methods for the copper‐mediated formation of carbon–carbon bonds illustrated by different coupling reactions: cross‐dehydrogenative coupling, decarboxylative cross‐coupling, Sonogashira‐type reactions, Suzuki‐type reactions, and Neigishi‐type reactions. Domino reactions and, finally, more atypical reactions are also illustrated. An overview of copper‐catalyzed C–C bond reactions through the main recently developed methodologies is presented.
AbstractList Copper-catalyzed cross-coupling reactions have found widespread application in carbon-carbon or carbon-heteroatom bond formation. The relatively low toxicity, ease of handling, and low cost of these versatile complexes make them attractive for the elaboration of new methodologies and for the obtaining of new compounds. We focus on recent methods for the copper-mediated formation of carbon-carbon bonds illustrated by different coupling reactions: cross-dehydrogenative coupling, decarboxylative cross-coupling, Sonogashira-type reactions, Suzuki-type reactions, and Neigishi-type reactions. Domino reactions and, finally, more atypical reactions are also illustrated.
Copper‐catalyzed cross‐coupling reactions have found widespread application in carbon–carbon or carbon–heteroatom bond formation. The relatively low toxicity, ease of handling, and low cost of these versatile complexes make them attractive for the elaboration of new methodologies and for the obtaining of new compounds. We focus on recent methods for the copper‐mediated formation of carbon–carbon bonds illustrated by different coupling reactions: cross‐dehydrogenative coupling, decarboxylative cross‐coupling, Sonogashira‐type reactions, Suzuki‐type reactions, and Neigishi‐type reactions. Domino reactions and, finally, more atypical reactions are also illustrated. An overview of copper‐catalyzed C–C bond reactions through the main recently developed methodologies is presented.
Author Maaliki, Carine
Thibonnet, Jérôme
Thiery, Emilie
Author_xml – sequence: 1
  givenname: Carine
  surname: Maaliki
  fullname: Maaliki, Carine
  organization: Université François‐Rabelais
– sequence: 2
  givenname: Emilie
  surname: Thiery
  fullname: Thiery, Emilie
  email: emilie.thiery@univ‐tours.fr
  organization: Université François‐Rabelais
– sequence: 3
  givenname: Jérôme
  surname: Thibonnet
  fullname: Thibonnet, Jérôme
  email: jerome.thibonnet@univ‐tours.fr
  organization: Université François‐Rabelais
BackLink https://hal.science/hal-01601331$$DView record in HAL
BookMark eNqFkL9OwzAQxi1UJNrCyhyJiSHlzk6ceCxRS0FFXUBis5zYgVRtHJwW1K2PgMQb9klICIKR6f79vtPdNyC90paGkHOEEQLQK7O02YgCcoAwgCPSRxDCBy6g1-QBC3wU7OmEDOp6CQCCc-yTaLI27tmUmfFs7iW2qow77D_ujS7Uxmhvat1abQpbfo8P-8_Eu7alrk_Jca5WtTn7iUPyOJ08JDN_vri5TcZzP2MCwWdIkYZZSNNI57ESGgKhVRwy1dwYITNRmuswyDHjlEFgmjqKUqFA6ZTTXLMhuez2vqiVrFyxVm4nrSrkbDyXba_9FxnDN2zYi46tnH3dmnojl3bryuY8iXEoAow5Yw016qjM2bp2Jv9diyBbI2VrpPw1shGITvBerMzuH1pO7hbJn_YLA5F30w
CitedBy_id crossref_primary_10_1016_j_jorganchem_2019_121014
crossref_primary_10_1016_j_jcat_2020_08_019
crossref_primary_10_1039_D1CC04002B
crossref_primary_10_1039_C7DT03510A
crossref_primary_10_1021_jacs_2c11563
crossref_primary_10_1002_chem_202100872
crossref_primary_10_1002_ejoc_201800827
crossref_primary_10_1039_D0DT03593A
crossref_primary_10_1021_acs_orglett_7b02764
crossref_primary_10_1016_j_mencom_2019_07_005
crossref_primary_10_1002_anie_201806169
crossref_primary_10_1002_ange_201701690
crossref_primary_10_1039_C7NJ02114C
crossref_primary_10_1039_C8SC01949E
crossref_primary_10_1016_j_tet_2018_08_051
crossref_primary_10_2174_0113852728262662230922075916
crossref_primary_10_1002_slct_202400334
crossref_primary_10_1021_acs_joc_8b00353
crossref_primary_10_3390_catal11101252
crossref_primary_10_1007_s11172_018_2093_8
crossref_primary_10_1016_j_tet_2018_10_068
crossref_primary_10_1021_acs_oprd_2c00050
crossref_primary_10_1039_D1QO00568E
crossref_primary_10_1002_anie_201701690
crossref_primary_10_1039_D3OB01231J
crossref_primary_10_1016_j_tetlet_2020_152601
crossref_primary_10_1039_C7OB02505J
crossref_primary_10_1007_s12039_018_1474_8
crossref_primary_10_1016_j_tetlet_2020_152083
crossref_primary_10_1039_C7CY01343D
crossref_primary_10_1002_slct_201903695
crossref_primary_10_1039_C7SC01968H
crossref_primary_10_1002_ange_201806169
crossref_primary_10_6023_A21010006
crossref_primary_10_1021_acs_chemrev_1c00383
crossref_primary_10_1080_10426507_2022_2116635
crossref_primary_10_1016_j_jcat_2019_04_003
crossref_primary_10_1016_j_mcat_2023_112915
crossref_primary_10_3390_catal8090359
crossref_primary_10_1016_j_ccr_2018_08_007
crossref_primary_10_3389_fmats_2019_00273
crossref_primary_10_6023_A21120608
crossref_primary_10_3390_molecules28041769
crossref_primary_10_1080_02603594_2016_1261023
crossref_primary_10_3390_knowledge3010001
crossref_primary_10_1039_C9NJ00684B
crossref_primary_10_1021_acscatal_0c03494
crossref_primary_10_1039_C8CC07032F
crossref_primary_10_1002_cjoc_202000075
crossref_primary_10_1021_acs_oprd_3c00260
crossref_primary_10_1021_acs_chemrev_8b00507
crossref_primary_10_1021_acs_joc_2c02882
Cites_doi 10.1055/s-0034-1380462
10.1021/jo3015819
10.1002/aoc.3298
10.1021/jo0623742
10.1002/chem.201503361
10.1039/C4RA02529F
10.1021/acs.orglett.6b00289
10.1016/S0040-4039(03)01174-2
10.1002/anie.200704782
10.1055/s-0032-1316542
10.1002/ange.201502379
10.1002/cplu.201300117
10.1002/anie.201007733
10.1021/cr100346g
10.1021/cr00104a001
10.1021/jm058173s
10.1055/s-0028-1083201
10.1002/cber.190103402141
10.1002/ange.200201617
10.1021/ja307783w
10.1002/ejoc.200500226
10.1039/c1ob05769c
10.1039/C5CC06645J
10.1021/jo502446k
10.1021/ol503482a
10.1007/3418_2012_32
10.1007/128_2009_17
10.1002/ange.200805122
10.1021/ja011018s
10.1002/anie.201204275
10.1039/C5CC08367B
10.1021/cr040664h
10.1021/jm801141f
10.1021/jo501137q
10.1002/adsc.201301091
10.1055/s-0031-1290376
10.1055/s-2007-966058
10.1039/C5OB00200A
10.1002/adsc.201200683
10.1002/anie.200805652
10.1002/ange.200604494
10.1021/ja027716
10.1073/pnas.1121005109
10.1021/jo052609u
10.1016/j.tet.2009.11.043
10.1002/ejoc.201402003
10.1002/anie.200804497
10.1002/asia.200900523
10.1021/ja0467768
10.1021/cr050992x
10.1002/9783527655588
10.1002/adsc.200900587
10.1055/s-2006-926372
10.1002/chem.201405223
10.1021/ol5030103
10.1002/adsc.201500803
10.1002/ange.200500368
10.1002/anie.200603451
10.1021/ja507704b
10.1021/ol503111h
10.1021/acs.joc.5b02077
10.1002/ejoc.201500706
10.1021/acs.orglett.5b01845
10.1021/ja111401h
10.1002/anie.200605055
10.1021/cr068398q
10.1055/s-2006-942373
10.1002/tcr.201100024
10.1016/j.tet.2013.07.085
10.1002/3527600086
10.1039/c1cs15137a
10.1016/S0022-328X(00)81848-3
10.1021/ol4036159
10.1021/ol500310u
10.1002/anie.201502379
10.1021/cr60132a001
10.1021/jo400616r
10.1002/anie.201105123
10.1002/chem.201102570
10.1002/0470021209
10.1016/j.tetlet.2009.03.146
10.1039/C5SC01736J
10.1002/ange.201105123
10.1021/jo2015533
10.1002/anie.200805122
10.1039/C4OB02138J
10.1021/cr8002505
10.1039/b407090a
10.1021/jo201528u
10.1016/j.tetlet.2012.06.023
10.1021/ol8013717
10.1002/anie.200500368
10.1021/acscatal.5b02718
10.1002/chem.201403073
10.1002/anie.201002108
10.1002/ange.200704782
10.1021/cr400524q
10.1021/jo501489c
10.1021/ol035378r
10.1002/ange.201109027
10.1002/anie.201005741
10.1021/cr000664r
10.1016/S1872-2067(14)60217-5
10.1021/jo070547x
10.1016/j.tetlet.2015.04.018
10.1016/j.tetasy.2012.09.002
10.1039/c3sc21818j
10.1021/ja9109055
10.1016/j.tetlet.2015.08.075
10.1039/b401586j
10.1021/acscatal.5b00310
10.1002/ange.201002108
10.1016/j.bmc.2011.06.056
10.1039/c3np70071b
10.1002/ange.201005741
10.1002/cber.186900201183
10.1021/ja304848n
10.1002/cmdc.200700104
10.1002/9781118690659
10.1021/ja0516054
10.1002/cber.19200531110
10.1002/ange.200805652
10.1039/c2cc17871k
10.1016/j.tet.2012.06.003
10.1021/ol402701x
10.1111/j.1749-6632.2001.tb04036.x
10.1021/ol9000922
10.1002/ejoc.200800394
10.1055/s-0035-1560397
10.1002/ange.200804497
10.1002/anie.200201617
10.1021/cr0505268
10.1021/jm2013979
10.1021/ar800138a
10.1016/j.tetlet.2009.12.138
10.1016/j.tet.2010.01.026
10.1039/JR9290001870
10.1039/c1cs15093f
10.1002/ange.201204275
10.1002/anie.201109027
10.1002/ange.201008007
10.1002/adsc.201000180
10.1021/ar800039x
10.1002/ange.200605055
10.1021/cen-v082n036.p049
10.1039/C5SC02143J
10.1039/C5CC05677B
10.1002/chem.201300480
10.1002/anie.200904916
10.1073/pnas.0601687103
10.1021/ol201629n
10.1016/j.tet.2015.07.052
10.1016/S0040-4039(00)91094-3
10.1016/j.bmcl.2009.08.047
10.1021/acs.joc.5b01935
10.1021/acs.joc.5b00888
10.1002/ange.201101391
10.1016/j.tet.2006.06.069
10.1039/c3ra23230a
10.1002/ange.201007733
10.1016/j.tet.2014.02.022
10.1002/aoc.3291
10.1039/c4gc00038b
10.1021/acs.joc.5b00800
10.1021/jm8007823
10.1021/acs.orglett.5b01612
10.1016/0040-4039(93)89005-B
10.1055/s-0029-1217822
10.1002/chem.201102710
10.1021/ja050058j
10.1039/c2cc33203e
10.1021/np0605586
10.1002/adsc.201000062
10.1016/j.tet.2015.07.004
10.1039/C4QO00331D
10.1002/anie.200604494
10.1002/ejoc.201402416
10.1002/anie.201008007
10.1039/C4CY00868E
10.2174/138527212800564358
10.1002/chem.201402114
10.1002/adsc.201300459
10.1021/ja3004792
10.1002/ange.200904916
10.1016/j.tet.2015.12.012
10.1002/anie.201101391
10.1016/j.tetasy.2006.02.007
10.1002/ange.200603451
10.1039/c4cc00637b
10.1016/j.tet.2015.05.017
10.1039/C0OB00622J
10.1039/c2cc31577g
10.1039/c2cc34659a
10.1039/c3ra41000e
10.1021/ja056541b
10.1021/ol501140p
10.1016/j.tetlet.2013.02.007
10.1002/ejoc.201403274
10.1002/aoc.3361
10.1021/ar800164n
10.1021/ol400692b
ContentType Journal Article
Copyright 2017 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim
2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Distributed under a Creative Commons Attribution 4.0 International License
Copyright_xml – notice: 2017 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim
– notice: 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
– notice: Distributed under a Creative Commons Attribution 4.0 International License
DBID AAYXX
CITATION
1XC
VOOES
DOI 10.1002/ejoc.201600540
DatabaseName CrossRef
Hyper Article en Ligne (HAL)
Hyper Article en Ligne (HAL) (Open Access)
DatabaseTitle CrossRef
DatabaseTitleList
CrossRef
DeliveryMethod fulltext_linktorsrc
Discipline Chemistry
EISSN 1099-0690
EndPage 228
ExternalDocumentID oai_HAL_hal_01601331v1
4303482941
10_1002_ejoc_201600540
EJOC201600540
Genre reviewArticle
GroupedDBID -~X
.3N
.GA
05W
0R~
10A
1L6
1OC
33P
3SF
3WU
4.4
4ZD
50Y
50Z
51W
51X
52M
52N
52O
52P
52S
52T
52U
52W
52X
53G
5GY
5VS
66C
702
77Q
7PT
8-0
8-1
8-3
8-4
8-5
8UM
930
A03
AABCJ
AAESR
AAEVG
AAHHS
AANLZ
AAONW
AASGY
AAXRX
AAZKR
ABCQN
ABCUV
ABDBF
ABEML
ABIJN
ABJNI
ABLJU
ABPVW
ACAHQ
ACCFJ
ACCZN
ACGFS
ACIWK
ACNCT
ACPOU
ACSCC
ACXBN
ACXQS
ADBBV
ADEOM
ADIZJ
ADKYN
ADMGS
ADOZA
ADXAS
ADZMN
ADZOD
AEEZP
AEIGN
AEIMD
AENEX
AEQDE
AEUQT
AEUYR
AFBPY
AFFNX
AFFPM
AFGKR
AFPWT
AFZJQ
AHBTC
AITYG
AIURR
AIWBW
AJBDE
AJXKR
ALAGY
ALMA_UNASSIGNED_HOLDINGS
ALUQN
AMBMR
AMYDB
ATUGU
AUFTA
AZBYB
AZVAB
BAFTC
BDRZF
BFHJK
BHBCM
BMNLL
BMXJE
BNHUX
BROTX
BRXPI
BY8
CS3
D-E
D-F
DCZOG
DPXWK
DR2
DRFUL
DRSTM
EJD
F00
F01
F04
F5P
G-S
G.N
GNP
GODZA
H.T
H.X
HBH
HGLYW
HHY
HHZ
HZ~
IX1
J0M
JPC
KQQ
LATKE
LAW
LC2
LC3
LEEKS
LH4
LITHE
LOXES
LP6
LP7
LUTES
LW6
LYRES
MEWTI
MK4
MRFUL
MRSTM
MSFUL
MSSTM
MXFUL
MXSTM
N04
N05
N9A
NF~
NNB
O66
O9-
OIG
P2P
P2W
P2X
P4D
Q.N
Q11
QB0
QRW
R.K
ROL
RWI
RX1
SUPJJ
TN5
UB1
UPT
V2E
W8V
W99
WBFHL
WBKPD
WH7
WIH
WIK
WJL
WOHZO
WQJ
WRC
WXSBR
WYISQ
XG1
XPP
XV2
~IA
~WT
AAYXX
CITATION
.Y3
1XC
31~
ACBWZ
AI.
AZFZN
EBS
FEDTE
HF~
HVGLF
MVM
RNS
VH1
VOOES
XJT
XOL
ZCG
ID FETCH-LOGICAL-c3910-312125c52b7df8a9d049da853a054713e7bfd54f1c62304ee7b77b9a0adb62fd3
IEDL.DBID DR2
ISSN 1434-193X
IngestDate Tue Oct 15 15:21:37 EDT 2024
Thu Oct 10 18:09:43 EDT 2024
Fri Aug 23 00:44:10 EDT 2024
Sat Aug 24 01:01:40 EDT 2024
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 2
Keywords C-C coupling
carbon carbon bond
liaison carbone carbone
décarboxylation
déhydrogenase
domini reactions
decarboxylative coupling
dehydrogenative coupling
Copper
synthetic methods
Language English
License Distributed under a Creative Commons Attribution 4.0 International License: http://creativecommons.org/licenses/by/4.0
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c3910-312125c52b7df8a9d049da853a054713e7bfd54f1c62304ee7b77b9a0adb62fd3
ORCID 0000-0001-7236-8232
0000-0003-3817-210X
OpenAccessLink https://hal.science/hal-01601331
PQID 1859418633
PQPubID 986364
PageCount 20
ParticipantIDs hal_primary_oai_HAL_hal_01601331v1
proquest_journals_1859418633
crossref_primary_10_1002_ejoc_201600540
wiley_primary_10_1002_ejoc_201600540_EJOC201600540
PublicationCentury 2000
PublicationDate January 10, 2017
PublicationDateYYYYMMDD 2017-01-10
PublicationDate_xml – month: 01
  year: 2017
  text: January 10, 2017
  day: 10
PublicationDecade 2010
PublicationPlace Weinheim
PublicationPlace_xml – name: Weinheim
PublicationTitle European journal of organic chemistry
PublicationYear 2017
Publisher Wiley Subscription Services, Inc
Wiley-VCH Verlag
Publisher_xml – name: Wiley Subscription Services, Inc
– name: Wiley-VCH Verlag
References 2013; 3
2015; 71
2007 2015; 72 29
2009 2009; 48 121
1975; 16
2006 2009 2010; 103 42 292
2004; 6
2007 1990 2007 2014; 70 90 107 114
2014 2015; 16 2
1972; 42
2007; 72
2015; 80
2014; 136
2014; 20
2012 2014; 134 20
2009; 11
1993; 34
2002 2008 2009 2009 2012 2013 2015; 108 48 121 4 13
2012; 134
2013; 54
1995 2012 2014
2014; 16
2010; 352
2008; 23
2013; 355
2012; 23
2010; 5
2016; 48
2003; 44
2015; 56
2009 2012; 19 55
2015; 51
2011; 76
2010 2010; 49 122
2005 2015; 36
2003 2003 2005 2005 2007; 42 115 44 117 107
2016; 18
2011; 133
2011; 9
2006 2007
2012 2012; 42 16
1997 2001 2007 2011 2012; 49 949 2 40 109
2016; 6
2006 2008
1948; 42
2012; 354
1920; 53
2013; 78
2002; 124
2009 2009 2012; 48 121 48
2005; 127
2011 2011; 50 123
2010 2012; 132 23
2012; 48
1929
2013 2014; 69 356
2012; 44
2010; 51
2014 2014; 70
2006; 71
2005 2009; 48 52
2004; 126
2007 2007 2008 2008; 46 119 47 120
2016; 72
2004 2008 2011 2015; 104 41 4
1869; 2
2011; 17
2012; 53
2008 2008 2011; 51 19
2013; 19
2010; 66
2013; 15
2014; 4
2004 2004 2004 2005 2005 2006 2007 2009 2011 2013; 82 44 117 106 351 111 30
2006; 62
2011 2011; 13 11
2012 2012; 51 124
2015 2015; 54 127
2003; 5
2016; 358
2016; 81
2012; 68
2014; 50
2001 2007 2007; 123 46 119
2006; 128
2015; 13
2015; 6
2015; 17
2015; 5
2011
1919; 52
2006; 17
2011; 40
1955 1957; 241 2
2009
2016; 52
2008; 10
2004
2012; 77
1901 2002; 34 102
2009 2009; 50
2015; 26
2015; 29
2005 2005; 127
2007 2007 2008; 46 119 41
2015; 21
2014; 79
2015
2014
e_1_2_9_71_5
e_1_2_9_71_4
e_1_2_9_71_3
e_1_2_9_71_2
e_1_2_9_79_1
e_1_2_9_94_1
e_1_2_9_10_1
e_1_2_9_56_1
e_1_2_9_94_2
e_1_2_9_33_1
e_1_2_9_71_1
e_1_2_9_107_1
e_1_2_9_122_1
e_1_2_9_145_1
e_1_2_9_18_1
e_1_2_9_60_5
e_1_2_9_60_4
e_1_2_9_60_3
e_1_2_9_60_2
e_1_2_9_22_1
e_1_2_9_45_1
e_1_2_9_68_1
e_1_2_9_83_1
e_1_2_9_45_2
e_1_2_9_6_1
e_1_2_9_119_1
e_1_2_9_111_1
e_1_2_9_134_1
e_1_2_9_45_3
e_1_2_9_72_1
e_1_2_9_11_1
e_1_2_9_34_1
e_1_2_9_57_1
e_1_2_9_95_1
e_1_2_9_95_2
Chodkiewicz W. (e_1_2_9_66_1) 1955; 241
e_1_2_9_129_2
e_1_2_9_129_1
e_1_2_9_144_1
e_1_2_9_106_1
e_1_2_9_57_2
e_1_2_9_121_1
e_1_2_9_19_1
e_1_2_9_61_1
e_1_2_9_46_1
e_1_2_9_84_1
e_1_2_9_23_1
e_1_2_9_5_2
e_1_2_9_5_1
e_1_2_9_3_10
Tamaru Y. (e_1_2_9_89_1) 2005
e_1_2_9_118_1
e_1_2_9_133_1
e_1_2_9_69_2
e_1_2_9_69_1
e_1_2_9_110_1
Zucchi R. (e_1_2_9_60_1) 1997; 49
e_1_2_9_31_1
e_1_2_9_77_1
e_1_2_9_54_1
e_1_2_9_92_1
e_1_2_9_109_1
e_1_2_9_124_3
e_1_2_9_101_2
e_1_2_9_147_2
e_1_2_9_101_1
e_1_2_9_124_1
e_1_2_9_147_1
e_1_2_9_124_2
e_1_2_9_39_1
e_1_2_9_16_1
e_1_2_9_39_2
e_1_2_9_20_1
e_1_2_9_89_2
e_1_2_9_43_1
e_1_2_9_8_1
e_1_2_9_81_1
e_1_2_9_113_1
e_1_2_9_8_2
e_1_2_9_136_1
e_1_2_9_28_1
e_1_2_9_78_2
e_1_2_9_78_1
e_1_2_9_32_1
e_1_2_9_55_1
e_1_2_9_108_2
e_1_2_9_93_1
e_1_2_9_108_1
e_1_2_9_70_1
Panda N. (e_1_2_9_5_4) 2015; 4
e_1_2_9_100_1
e_1_2_9_123_1
e_1_2_9_146_1
e_1_2_9_17_1
(e_1_2_9_2_2) 2012
e_1_2_9_44_2
e_1_2_9_21_1
e_1_2_9_67_1
e_1_2_9_44_1
e_1_2_9_7_1
e_1_2_9_82_1
e_1_2_9_112_1
Beletskaya I. P. (e_1_2_9_135_1) 2014
e_1_2_9_29_1
e_1_2_9_52_2
e_1_2_9_75_1
e_1_2_9_98_1
e_1_2_9_52_1
e_1_2_9_52_3
e_1_2_9_90_1
e_1_2_9_103_1
e_1_2_9_126_1
e_1_2_9_14_1
e_1_2_9_141_1
e_1_2_9_37_1
e_1_2_9_41_1
e_1_2_9_64_1
e_1_2_9_87_1
e_1_2_9_87_2
e_1_2_9_2_3
Muller T. J. J. (e_1_2_9_3_7) 2007
e_1_2_9_138_1
e_1_2_9_138_2
Thakur K. G. (e_1_2_9_80_2) 2009
e_1_2_9_115_1
e_1_2_9_26_1
e_1_2_9_49_1
e_1_2_9_49_2
e_1_2_9_130_1
e_1_2_9_49_3
e_1_2_9_49_4
e_1_2_9_30_1
e_1_2_9_53_1
e_1_2_9_99_1
e_1_2_9_53_2
e_1_2_9_76_1
e_1_2_9_91_1
e_1_2_9_91_2
e_1_2_9_91_3
e_1_2_9_102_1
e_1_2_9_148_1
Chodkiewicz W. (e_1_2_9_66_2) 1957; 2
e_1_2_9_125_1
e_1_2_9_15_1
e_1_2_9_38_1
e_1_2_9_140_1
e_1_2_9_15_3
e_1_2_9_15_2
e_1_2_9_42_1
e_1_2_9_88_1
Su Y. (e_1_2_9_5_3) 2011
e_1_2_9_65_1
e_1_2_9_80_1
e_1_2_9_114_1
e_1_2_9_137_1
e_1_2_9_27_1
e_1_2_9_50_1
e_1_2_9_73_1
e_1_2_9_35_1
e_1_2_9_96_1
e_1_2_9_12_1
Corey E. J. (e_1_2_9_2_1) 1995
e_1_2_9_128_1
e_1_2_9_105_2
e_1_2_9_105_1
e_1_2_9_35_2
e_1_2_9_120_1
e_1_2_9_58_1
e_1_2_9_143_1
e_1_2_9_62_1
e_1_2_9_24_1
e_1_2_9_85_1
e_1_2_9_4_5
e_1_2_9_4_4
e_1_2_9_4_3
e_1_2_9_4_2
e_1_2_9_4_1
Rosenmund K. W. (e_1_2_9_9_1) 1919; 52
e_1_2_9_117_1
e_1_2_9_4_7
e_1_2_9_4_6
e_1_2_9_24_2
e_1_2_9_47_1
e_1_2_9_132_1
e_1_2_9_51_2
e_1_2_9_97_2
e_1_2_9_74_1
e_1_2_9_51_1
e_1_2_9_13_1
e_1_2_9_97_1
King A. O. (e_1_2_9_3_3) 2004
e_1_2_9_127_1
e_1_2_9_104_1
e_1_2_9_13_2
e_1_2_9_36_1
e_1_2_9_59_1
e_1_2_9_142_1
e_1_2_9_142_2
e_1_2_9_40_2
e_1_2_9_63_1
e_1_2_9_40_1
e_1_2_9_86_1
e_1_2_9_3_6
e_1_2_9_3_5
e_1_2_9_3_4
e_1_2_9_116_4
e_1_2_9_3_2
e_1_2_9_3_1
e_1_2_9_139_1
e_1_2_9_139_2
e_1_2_9_116_3
e_1_2_9_3_9
e_1_2_9_116_2
e_1_2_9_3_8
e_1_2_9_116_1
e_1_2_9_25_2
e_1_2_9_25_1
e_1_2_9_131_1
e_1_2_9_48_1
References_xml – year: 2011
– volume: 127
  start-page: 3173 3672
  year: 2005 2005
  end-page: 3176 3673
  publication-title: Eur. J. Org. Chem. J. Am. Chem. Soc.
– volume: 29
  start-page: 353
  year: 2015
  end-page: 356
  publication-title: Appl. Organomet. Chem.
– volume: 9
  start-page: 1212
  year: 2011
  end-page: 1218
  publication-title: Org. Biomol. Chem.
– volume: 13 11
  start-page: 4288 236
  year: 2011 2011
  end-page: 4291 241
  publication-title: Org. Lett. Chem. Rec.
– start-page: 281
  year: 2014
  end-page: 312
– volume: 6
  start-page: 1540
  year: 2016
  end-page: 1552
  publication-title: ACS Catal.
– volume: 108 48 121 4 13
  start-page: 3054 6954 7088 2301 4816
  year: 2002 2008 2009 2009 2012 2013 2015
  end-page: 3131 6971 2318 4827
  publication-title: Chem. Rev. Angew. Chem. Int. Ed. Angew. Chem. Chem. Sci. Org. Biomol. Chem.
– volume: 126
  start-page: 10240
  year: 2004
  end-page: 10241
  publication-title: J. Am. Chem. Soc.
– volume: 34
  start-page: 761
  year: 1993
  end-page: 764
  publication-title: Tetrahedron Lett.
– volume: 16
  start-page: 6342
  year: 2014
  end-page: 6345
  publication-title: Org. Lett.
– volume: 48 121
  start-page: 792 806
  year: 2009 2009
  end-page: 795
  publication-title: Angew. Chem. Int. Ed. Angew. Chem.
– volume: 48
  start-page: 7847
  year: 2012
  end-page: 7849
  publication-title: Chem. Commun.
– volume: 17
  start-page: 3982
  year: 2015
  end-page: 3985
  publication-title: Org. Lett.
– volume: 127
  start-page: 6968
  year: 2005
  end-page: 6969
  publication-title: J. Am. Chem. Soc.
– volume: 46 119 41
  start-page: 2086 2132 1545
  year: 2007 2007 2008
  end-page: 2089 1554
  publication-title: Angew. Chem. Int. Ed. Angew. Chem. Acc. Chem. Res.
– volume: 69 356
  start-page: 8579 1703
  year: 2013 2014
  end-page: 8582 1707
  publication-title: Tetrahedron Adv. Synth. Catal.
– volume: 134
  start-page: 5742
  year: 2012
  end-page: 5745
  publication-title: J. Am. Chem. Soc.
– volume: 13
  start-page: 447
  year: 2015
  end-page: 451
  publication-title: Org. Biomol. Chem. Org. Biol. Mol.
– volume: 80
  start-page: 7251
  year: 2015
  end-page: 7257
  publication-title: J. Org. Chem.
– volume: 82 44 117 106 351 111 30
  start-page: 49 205 4442 4516 2651 3027 2177 1467
  year: 2004 2004 2004 2005 2005 2006 2007 2009 2011 2013
  end-page: 58 246 4489 2710 3043 2250 1489
  publication-title: Chem. Eng. News Angew. Chem. Int. Ed. Angew. Chem. Chem. Rev. Adv. Synth. Catal. Chem. Rev. Nat. Prod. Rep.
– volume: 50
  start-page: 2865 2785
  year: 2009 2009
  end-page: 2869 2789
  publication-title: Tetrahedron Lett. Synthesis
– start-page: 3646
  year: 2014
  end-page: 3655
  publication-title: Eur. J. Org. Chem.
– volume: 51 124
  start-page: 9110 9244
  year: 2012 2012
  end-page: 9113
  publication-title: Angew. Chem. Int. Ed. Angew. Chem.
– volume: 16
  start-page: 4467
  year: 1975
  end-page: 4470
  publication-title: Tetrahedron Lett.
– volume: 72
  start-page: 4844
  year: 2007
  end-page: 4850
  publication-title: J. Org. Chem.
– volume: 16
  start-page: 2428
  year: 2014
  end-page: 2431
  publication-title: Green Chem.
– volume: 56
  start-page: 5676
  year: 2015
  end-page: 5680
  publication-title: Tetrahedron Lett.
– volume: 76
  start-page: 8347
  year: 2011
  end-page: 8354
  publication-title: J. Org. Chem.
– volume: 78
  start-page: 943
  year: 2013
  end-page: 951
  publication-title: ChemPlusChem
– volume: 48 52
  start-page: 3953 1018
  year: 2005 2009
  end-page: 3979 1028
  publication-title: J. Med. Chem. J. Med. Chem.
– volume: 23
  start-page: 1393
  year: 2012
  end-page: 1399
  publication-title: Tetrahedron: Asymmetry
– volume: 56
  start-page: 2720
  year: 2015
  end-page: 2723
  publication-title: Tetrahedron Lett.
– volume: 50 123
  start-page: 3904 3990
  year: 2011 2011
  end-page: 3907
  publication-title: Angew. Chem. Int. Ed. Angew. Chem.
– volume: 136
  start-page: 11590
  year: 2014
  end-page: 11593
  publication-title: J. Am. Chem. Soc.
– volume: 17
  start-page: 590
  year: 2006
  end-page: 597
  publication-title: Tetrahedron: Asymmetry
– volume: 358
  start-page: 67
  year: 2016
  end-page: 73
  publication-title: Adv. Synth. Catal.
– start-page: 1934
  year: 2004
  end-page: 1935
  publication-title: Chem. Commun.
– volume: 16
  start-page: 844
  year: 2014
  end-page: 847
  publication-title: Org. Lett.
– volume: 52
  start-page: 1432
  year: 2016
  end-page: 1435
  publication-title: Chem. Commun.
– volume: 16
  start-page: 6144
  year: 2014
  end-page: 6147
  publication-title: Org. Lett.
– volume: 6
  start-page: 5882
  year: 2015
  end-page: 5890
  publication-title: Chem. Sci.
– volume: 72
  start-page: 645
  year: 2016
  end-page: 652
  publication-title: Tetrahedron
– start-page: 2457
  year: 2009
  end-page: 2460
  publication-title: Synlett
– volume: 48 121 48
  start-page: 1636 1664 3064
  year: 2009 2009 2012
  end-page: 1639 3066
  publication-title: Angew. Chem. Int. Ed. Angew. Chem. Chem. Commun.
– volume: 11
  start-page: 1309
  year: 2009
  end-page: 1312
  publication-title: Org. Lett.
– volume: 42 115 44 117 107
  start-page: 1566 1604 4442 4516 874
  year: 2003 2003 2005 2005 2007
  end-page: 1568 4489 922
  publication-title: Angew. Chem. Int. Ed. Angew. Chem. Angew. Chem. Int. Ed. Angew. Chem. Chem. Rev.
– volume: 241 2
  start-page: 1055 819
  year: 1955 1957
  end-page: 1057 869
  publication-title: Hebd. Seances Acad. Sci. Ann. Chim. (Paris)
– volume: 54 127
  start-page: 8236 8354
  year: 2015 2015
  end-page: 8240
  publication-title: Angew. Chem. Int. Ed. Angew. Chem.
– volume: 48 121
  start-page: 9350 9514
  year: 2009 2009
  end-page: 9354
  publication-title: Angew. Chem. Int. Ed. Angew. Chem.
– volume: 52
  start-page: 1746
  year: 1919
  end-page: 1749
  publication-title: Ber. Dtsch. Chem. Ges.
– volume: 3
  start-page: 18283
  year: 2013
  end-page: 18287
  publication-title: RSC Adv.
– volume: 81
  start-page: 787
  year: 2016
  end-page: 802
  publication-title: J. Org. Chem.
– volume: 71
  start-page: 2802
  year: 2006
  end-page: 2810
  publication-title: J. Org. Chem.
– volume: 16
  start-page: 3024
  year: 2014
  end-page: 3027
  publication-title: Org. Lett.
– volume: 3
  start-page: 6278
  year: 2013
  end-page: 6281
  publication-title: RSC Adv.
– volume: 15
  start-page: 5378
  year: 2013
  end-page: 5381
  publication-title: Org. Lett.
– volume: 355
  start-page: 2936
  year: 2013
  end-page: 2941
  publication-title: Adv. Synth. Catal.
– volume: 44
  start-page: 2374
  year: 2012
  end-page: 2384
  publication-title: Synthesis
– volume: 34 102
  start-page: 2174 1359
  year: 1901 2002
  end-page: 2185 1470
  publication-title: Ber. Dtsch. Chem. Ges. Chem. Rev.
– volume: 53
  start-page: 2226
  year: 1920
  end-page: 2240
  publication-title: Ber. Dtsch. Chem. Ges.
– volume: 50 123
  start-page: 1114 1146
  year: 2011 2011
  end-page: 1117
  publication-title: Angew. Chem. Int. Ed. Angew. Chem.
– volume: 51
  start-page: 15756
  year: 2015
  end-page: 15759
  publication-title: Chem. Commun.
– volume: 53
  start-page: 4248
  year: 2012
  end-page: 4252
  publication-title: Tetrahedron Lett.
– volume: 20
  start-page: 8325
  year: 2014
  end-page: 8329
  publication-title: Chem. Eur. J.
– volume: 51
  start-page: 15059
  year: 2015
  end-page: 15062
  publication-title: Chem. Commun.
– volume: 4
  start-page: 4274
  year: 2014
  end-page: 4280
  publication-title: Catal. Sci. Technol.
– volume: 49 949 2 40 109
  start-page: 1 295 1520 5030 9629
  year: 1997 2001 2007 2011 2012
  end-page: 51 303 1526 5048 9634
  publication-title: Pharmacol. Rev. Ann. N. Y. Acad. Sci. ChemMedChem Chem. Soc. Rev. Proc. Natl. Acad. Sci. USA
– volume: 42
  start-page: 205
  year: 1972
  end-page: 228
  publication-title: J. Organomet. Chem.
– volume: 352
  start-page: 1582
  year: 2010
  end-page: 1586
  publication-title: Adv. Synth. Catal.
– volume: 48
  start-page: 504
  year: 2016
  end-page: 511
  publication-title: Synthesis
– volume: 66
  start-page: 80
  year: 2010
  end-page: 86
  publication-title: Tetrahedron
– start-page: 1870
  year: 1929
  end-page: 1873
  publication-title: J. Chem. Soc.
– volume: 71
  start-page: 6689
  year: 2015
  end-page: 6693
  publication-title: Tetrahedron
– volume: 54
  start-page: 2006
  year: 2013
  end-page: 2009
  publication-title: Tetrahedron Lett.
– volume: 5
  start-page: 2882
  year: 2015
  end-page: 2885
  publication-title: ACS Catal.
– volume: 5
  start-page: 74
  year: 2010
  end-page: 76
  publication-title: Chem. Asian J.
– volume: 18
  start-page: 2040
  year: 2016
  end-page: 2043
  publication-title: Org. Lett.
– volume: 6
  start-page: 215
  year: 2004
  end-page: 218
  publication-title: Green Chem.
– volume: 42
  start-page: 189
  year: 1948
  end-page: 283
  publication-title: Chem. Rev.
– volume: 50 123
  start-page: 10429 10613
  year: 2011 2011
  end-page: 10432
  publication-title: Angew. Chem. Int. Ed. Angew. Chem.
– volume: 133
  start-page: 2160
  year: 2011
  end-page: 2162
  publication-title: J. Am. Chem. Soc.
– volume: 80
  start-page: 1506
  year: 2015
  end-page: 1516
  publication-title: J. Org. Chem.
– volume: 76
  start-page: 9144
  year: 2011
  end-page: 9150
  publication-title: J. Org. Chem.
– volume: 354
  start-page: 3421
  year: 2012
  end-page: 3427
  publication-title: Adv. Synth. Catal.
– volume: 79
  start-page: 8689
  year: 2014
  end-page: 8699
  publication-title: J. Org. Chem.
– volume: 62
  start-page: 8559
  year: 2006
  end-page: 8563
  publication-title: Tetrahedron
– volume: 20
  start-page: 6618
  year: 2014
  end-page: 6621
  publication-title: Chem. Eur. J.
– volume: 40
  start-page: 4948
  year: 2011
  end-page: 4962
  publication-title: Chem. Soc. Rev.
– volume: 5
  start-page: 3843
  year: 2003
  end-page: 3846
  publication-title: Org. Lett.
– volume: 71
  start-page: 4418
  year: 2015
  end-page: 4425
  publication-title: Tetrahedron
– volume: 68
  start-page: 6413
  year: 2012
  end-page: 6419
  publication-title: Tetrahedron
– volume: 17
  start-page: 362
  year: 2015
  end-page: 365
  publication-title: Org. Lett.
– volume: 66
  start-page: 2077
  year: 2010
  end-page: 2082
  publication-title: Tetrahedron
– volume: 70
  start-page: 2416 4817
  year: 2014 2014
  end-page: 2421 4822
  publication-title: Tetrahedron Eur. J. Org. Chem.
– volume: 36
  start-page: 3
  year: 2005 2015
  end-page: 14
  publication-title: Chin. J. Catal.
– year: 1995 2012 2014
– volume: 352
  start-page: 1593
  year: 2010
  end-page: 1599
  publication-title: Adv. Synth. Catal.
– volume: 9
  start-page: 6873
  year: 2011
  end-page: 6894
  publication-title: Org. Biomol. Chem.
– volume: 23
  start-page: 4050
  year: 2008
  end-page: 4054
  publication-title: Eur. J. Org. Chem.
– volume: 134 20
  start-page: 11124 15334
  year: 2012 2014
  end-page: 11127 15338
  publication-title: J. Am. Chem. Soc. Chem. Eur. J.
– start-page: 1961 3591
  year: 2006 2008
  end-page: 1970 3600
  publication-title: Synthesis Synthesis
– volume: 103 42 292
  start-page: 8928 335 281
  year: 2006 2009 2010
  end-page: 8933 344 302
  publication-title: Proc. Natl. Acad. Sci. USA Acc. Chem. Res. Top. Curr. Chem.
– volume: 44
  start-page: 5011
  year: 2003
  end-page: 5013
  publication-title: Tetrahedron Lett.
– start-page: 876
  year: 2015
  end-page: 885
  publication-title: Eur. J. Org. Chem.
– start-page: 1155 1649
  year: 2006 2007
  end-page: 1161 1654
  publication-title: Synthesis Synthesis
– volume: 70 90 107 114
  start-page: 891 879 1892 6213
  year: 2007 1990 2007 2014
  end-page: 900 933 1918 6284
  publication-title: J. Nat. Prod. Chem. Rev. Chem. Rev. Chem. Rev.
– volume: 19 55
  start-page: 5569 475
  year: 2009 2012
  end-page: 5572 488
  publication-title: Bioorg. Med. Chem. Lett. J. Med. Chem.
– volume: 2
  start-page: 422
  year: 1869
  end-page: 424
  publication-title: Ber. Dtsch. Chem. Ges.
– volume: 4
  start-page: 21688
  year: 2014
  end-page: 21698
  publication-title: RSC Adv.
– volume: 79
  start-page: 8566
  year: 2014
  end-page: 8576
  publication-title: J. Org. Chem.
– volume: 19
  start-page: 8144
  year: 2013
  end-page: 8152
  publication-title: Chem. Eur. J.
– volume: 50
  start-page: 3589
  year: 2014
  end-page: 3591
  publication-title: Chem. Commun.
– volume: 132 23
  start-page: 5332 1686
  year: 2010 2012
  end-page: 5333 1690
  publication-title: J. Am. Chem. Soc. Synlett
– volume: 71
  start-page: 7010
  year: 2015
  end-page: 7015
  publication-title: Tetrahedron
– volume: 124
  start-page: 11858
  year: 2002
  end-page: 11859
  publication-title: J. Am. Chem. Soc.
– volume: 72 29
  start-page: 2053 787
  year: 2007 2015
  end-page: 2057 792
  publication-title: J. Org. Chem. Appl. Organomet. Chem.
– volume: 123 46 119
  start-page: 10183 4388 4467
  year: 2001 2007 2007
  end-page: 10190 4392
  publication-title: J. Am. Chem. Soc. Angew. Chem. Int. Ed. Angew. Chem.
– volume: 51
  start-page: 1287
  year: 2010
  end-page: 1290
  publication-title: Tetrahedron Lett.
– volume: 51 124
  start-page: 3453 3509
  year: 2012 2012
  end-page: 457
  publication-title: Angew. Chem. Int. Ed. Angew. Chem.
– volume: 134
  start-page: 16167
  year: 2012
  end-page: 16170
  publication-title: J. Am. Chem. Soc.
– volume: 50 123
  start-page: 2990 3046
  year: 2011 2011
  end-page: 2994
  publication-title: Angew. Chem. Int. Ed. Angew. Chem.
– volume: 6
  start-page: 5978
  year: 2015
  end-page: 5983
  publication-title: Chem. Sci.
– volume: 51 19
  start-page: 7777 4971
  year: 2008 2008 2011
  end-page: 7787 4984
  publication-title: J. Med. Chem. Bioorg. Med. Chem
– volume: 17
  start-page: 12561
  year: 2011
  end-page: 12563
  publication-title: Chem. Eur. J.
– volume: 80
  start-page: 11322
  year: 2015
  end-page: 11329
  publication-title: J. Org. Chem.
– volume: 128
  start-page: 56
  year: 2006
  end-page: 57
  publication-title: J. Am. Chem. Soc.
– volume: 48
  start-page: 5862
  year: 2012
  end-page: 5864
  publication-title: Chem. Commun.
– volume: 42 16
  start-page: 1 1128
  year: 2012 2012
  end-page: 34 1150
  publication-title: Top. Organomet. Chem. Curr. Org. Chem.
– volume: 48
  start-page: 10704
  year: 2012
  end-page: 10714
  publication-title: Chem. Commun.
– volume: 15
  start-page: 1802
  year: 2013
  end-page: 1805
  publication-title: Org. Lett.
– start-page: 5334
  year: 2015
  end-page: 5338
  publication-title: Eur. J. Org. Chem.
– volume: 80
  start-page: 7089
  year: 2015
  end-page: 7098
  publication-title: J. Org. Chem.
– volume: 21
  start-page: 18080
  year: 2015
  end-page: 18084
  publication-title: Chem. Eur. J.
– volume: 29
  start-page: 301
  year: 2015
  end-page: 304
  publication-title: Appl. Organomet. Chem.
– volume: 16 2
  start-page: 1264 649
  year: 2014 2015
  end-page: 1267 653
  publication-title: Org. Lett. Org. Chem. Front.
– volume: 17
  start-page: 3682
  year: 2015
  end-page: 3685
  publication-title: Org. Lett.
– volume: 17
  start-page: 13692
  year: 2011
  end-page: 13696
  publication-title: Chem. Eur. J.
– volume: 50 123
  start-page: 7140 7278
  year: 2011 2011
  end-page: 7143
  publication-title: Angew. Chem. Int. Ed. Angew. Chem.
– volume: 10
  start-page: 3607
  year: 2008
  end-page: 3609
  publication-title: Org. Lett.
– volume: 77
  start-page: 9379
  year: 2012
  end-page: 9383
  publication-title: J. Org. Chem.
– volume: 49 122
  start-page: 5558 5690
  year: 2010 2010
  end-page: 5562
  publication-title: Angew. Chem. Int. Ed. Angew. Chem.
– volume: 26
  start-page: 1649
  year: 2015
  end-page: 1664
  publication-title: Synlett
– volume: 46 119 47 120
  start-page: 1373 1395 3100 3144
  year: 2007 2007 2008 2008
  end-page: 1375 3120
  publication-title: Angew. Chem. Int. Ed. Angew. Chem. Angew. Chem. Int. Ed. Angew. Chem.
– volume: 104 41 4
  start-page: 6217 1500 1678 1
  year: 2004 2008 2011 2015
  end-page: 6254 1511 1690 21
  publication-title: Chem. Rev. Acc. Chem. Res. Synthesis Org. Chem. Curr. Res.
– volume: 78
  start-page: 4551
  year: 2013
  end-page: 4557
  publication-title: J. Org. Chem.
– ident: e_1_2_9_141_1
  doi: 10.1055/s-0034-1380462
– ident: e_1_2_9_77_1
  doi: 10.1021/jo3015819
– ident: e_1_2_9_82_1
  doi: 10.1002/aoc.3298
– ident: e_1_2_9_78_1
  doi: 10.1021/jo0623742
– ident: e_1_2_9_26_1
  doi: 10.1002/chem.201503361
– ident: e_1_2_9_75_1
  doi: 10.1039/C4RA02529F
– ident: e_1_2_9_148_1
  doi: 10.1021/acs.orglett.6b00289
– ident: e_1_2_9_72_1
  doi: 10.1016/S0040-4039(03)01174-2
– ident: e_1_2_9_49_3
  doi: 10.1002/anie.200704782
– ident: e_1_2_9_48_1
  doi: 10.1055/s-0032-1316542
– ident: e_1_2_9_108_2
  doi: 10.1002/ange.201502379
– ident: e_1_2_9_14_1
  doi: 10.1002/cplu.201300117
– ident: e_1_2_9_147_1
  doi: 10.1002/anie.201007733
– ident: e_1_2_9_3_9
  doi: 10.1021/cr100346g
– ident: e_1_2_9_116_2
  doi: 10.1021/cr00104a001
– ident: e_1_2_9_51_1
  doi: 10.1021/jm058173s
– ident: e_1_2_9_105_2
  doi: 10.1055/s-0028-1083201
– ident: e_1_2_9_8_1
  doi: 10.1002/cber.190103402141
– ident: e_1_2_9_71_2
  doi: 10.1002/ange.200201617
– ident: e_1_2_9_146_1
  doi: 10.1021/ja307783w
– ident: e_1_2_9_13_1
  doi: 10.1002/ejoc.200500226
– ident: e_1_2_9_110_1
  doi: 10.1039/c1ob05769c
– start-page: 281
  volume-title: Modern copper‐catalyzed Hurtley reaction: efficient C‐arylation of C‐H acid, Copper‐mediated cross‐coupling reactions
  year: 2014
  ident: e_1_2_9_135_1
  contributor:
    fullname: Beletskaya I. P.
– ident: e_1_2_9_55_1
  doi: 10.1039/C5CC06645J
– ident: e_1_2_9_103_1
  doi: 10.1021/jo502446k
– ident: e_1_2_9_114_1
  doi: 10.1021/ol503482a
– ident: e_1_2_9_87_1
  doi: 10.1007/3418_2012_32
– ident: e_1_2_9_15_3
  doi: 10.1007/128_2009_17
– ident: e_1_2_9_57_2
  doi: 10.1002/ange.200805122
– ident: e_1_2_9_52_1
  doi: 10.1021/ja011018s
– ident: e_1_2_9_94_1
  doi: 10.1002/anie.201204275
– ident: e_1_2_9_56_1
  doi: 10.1039/C5CC08367B
– ident: e_1_2_9_5_1
  doi: 10.1021/cr040664h
– ident: e_1_2_9_51_2
  doi: 10.1021/jm801141f
– ident: e_1_2_9_115_1
  doi: 10.1021/jo501137q
– ident: e_1_2_9_24_2
  doi: 10.1002/adsc.201301091
– ident: e_1_2_9_142_2
  doi: 10.1055/s-0031-1290376
– ident: e_1_2_9_138_2
  doi: 10.1055/s-2007-966058
– ident: e_1_2_9_7_1
– ident: e_1_2_9_4_7
  doi: 10.1039/C5OB00200A
– ident: e_1_2_9_84_1
  doi: 10.1002/adsc.201200683
– ident: e_1_2_9_45_1
  doi: 10.1002/anie.200805652
– ident: e_1_2_9_49_2
  doi: 10.1002/ange.200604494
– ident: e_1_2_9_100_1
  doi: 10.1021/ja027716
– ident: e_1_2_9_60_5
  doi: 10.1073/pnas.1121005109
– ident: e_1_2_9_137_1
  doi: 10.1021/jo052609u
– ident: e_1_2_9_131_1
  doi: 10.1016/j.tet.2009.11.043
– ident: e_1_2_9_102_1
  doi: 10.1002/ejoc.201402003
– volume: 4
  start-page: 1
  year: 2015
  ident: e_1_2_9_5_4
  publication-title: Org. Chem. Curr. Res.
  contributor:
    fullname: Panda N.
– ident: e_1_2_9_4_3
  doi: 10.1002/anie.200804497
– ident: e_1_2_9_125_1
  doi: 10.1002/asia.200900523
– ident: e_1_2_9_106_1
  doi: 10.1021/ja0467768
– ident: e_1_2_9_71_5
  doi: 10.1021/cr050992x
– ident: e_1_2_9_2_3
  doi: 10.1002/9783527655588
– ident: e_1_2_9_3_8
  doi: 10.1002/adsc.200900587
– ident: e_1_2_9_138_1
  doi: 10.1055/s-2006-926372
– ident: e_1_2_9_95_2
  doi: 10.1002/chem.201405223
– start-page: 205
  volume-title: Palladium‐Catalyzed Cross‐Coupling Reactions in the Synthesis of Pharmaceuticals
  year: 2004
  ident: e_1_2_9_3_3
  contributor:
    fullname: King A. O.
– ident: e_1_2_9_96_1
  doi: 10.1021/ol5030103
– ident: e_1_2_9_36_1
  doi: 10.1002/adsc.201500803
– ident: e_1_2_9_3_5
  doi: 10.1002/ange.200500368
– ident: e_1_2_9_124_2
– ident: e_1_2_9_91_1
  doi: 10.1002/anie.200603451
– ident: e_1_2_9_42_1
  doi: 10.1021/ja507704b
– ident: e_1_2_9_98_1
  doi: 10.1021/ol503111h
– ident: e_1_2_9_111_1
  doi: 10.1021/acs.joc.5b02077
– ident: e_1_2_9_30_1
  doi: 10.1002/ejoc.201500706
– volume: 241
  start-page: 1055
  year: 1955
  ident: e_1_2_9_66_1
  publication-title: Hebd. Seances Acad. Sci.
  contributor:
    fullname: Chodkiewicz W.
– ident: e_1_2_9_107_1
  doi: 10.1021/acs.orglett.5b01845
– ident: e_1_2_9_34_1
  doi: 10.1021/ja111401h
– ident: e_1_2_9_52_2
  doi: 10.1002/anie.200605055
– ident: e_1_2_9_116_3
  doi: 10.1021/cr068398q
– start-page: 1678
  year: 2011
  ident: e_1_2_9_5_3
  publication-title: Synthesis
  contributor:
    fullname: Su Y.
– ident: e_1_2_9_105_1
  doi: 10.1055/s-2006-942373
– ident: e_1_2_9_25_2
  doi: 10.1002/tcr.201100024
– ident: e_1_2_9_24_1
  doi: 10.1016/j.tet.2013.07.085
– ident: e_1_2_9_4_1
  doi: 10.1002/3527600086
– ident: e_1_2_9_86_1
  doi: 10.1039/c1cs15137a
– ident: e_1_2_9_90_1
  doi: 10.1016/S0022-328X(00)81848-3
– ident: e_1_2_9_92_1
  doi: 10.1021/ol4036159
– ident: e_1_2_9_101_1
  doi: 10.1021/ol500310u
– ident: e_1_2_9_108_1
  doi: 10.1002/anie.201502379
– ident: e_1_2_9_11_1
  doi: 10.1021/cr60132a001
– ident: e_1_2_9_68_1
  doi: 10.1021/jo400616r
– ident: e_1_2_9_40_1
  doi: 10.1002/anie.201105123
– ident: e_1_2_9_122_1
  doi: 10.1002/chem.201102570
– ident: e_1_2_9_3_1
  doi: 10.1002/0470021209
– ident: e_1_2_9_80_1
  doi: 10.1016/j.tetlet.2009.03.146
– ident: e_1_2_9_46_1
  doi: 10.1039/C5SC01736J
– ident: e_1_2_9_40_2
  doi: 10.1002/ange.201105123
– ident: e_1_2_9_20_1
  doi: 10.1021/jo2015533
– ident: e_1_2_9_57_1
  doi: 10.1002/anie.200805122
– ident: e_1_2_9_18_1
  doi: 10.1039/C4OB02138J
– ident: e_1_2_9_4_2
  doi: 10.1021/cr8002505
– ident: e_1_2_9_73_1
  doi: 10.1039/b407090a
– ident: e_1_2_9_123_1
  doi: 10.1021/jo201528u
– ident: e_1_2_9_61_1
  doi: 10.1016/j.tetlet.2012.06.023
– ident: e_1_2_9_104_1
  doi: 10.1021/ol8013717
– ident: e_1_2_9_71_3
  doi: 10.1002/anie.200500368
– ident: e_1_2_9_88_1
  doi: 10.1021/acscatal.5b02718
– ident: e_1_2_9_50_1
  doi: 10.1002/chem.201403073
– ident: e_1_2_9_39_1
  doi: 10.1002/anie.201002108
– ident: e_1_2_9_49_4
  doi: 10.1002/ange.200704782
– ident: e_1_2_9_116_4
  doi: 10.1021/cr400524q
– ident: e_1_2_9_133_1
  doi: 10.1021/jo501489c
– ident: e_1_2_9_128_1
  doi: 10.1021/ol035378r
– ident: e_1_2_9_35_2
  doi: 10.1002/ange.201109027
– ident: e_1_2_9_139_1
  doi: 10.1002/anie.201005741
– ident: e_1_2_9_8_2
  doi: 10.1021/cr000664r
– ident: e_1_2_9_89_2
  doi: 10.1016/S1872-2067(14)60217-5
– ident: e_1_2_9_126_1
  doi: 10.1021/jo070547x
– ident: e_1_2_9_58_1
  doi: 10.1016/j.tetlet.2015.04.018
– ident: e_1_2_9_93_1
  doi: 10.1016/j.tetasy.2012.09.002
– ident: e_1_2_9_4_5
  doi: 10.1039/c3sc21818j
– ident: e_1_2_9_142_1
  doi: 10.1021/ja9109055
– ident: e_1_2_9_59_1
  doi: 10.1016/j.tetlet.2015.08.075
– ident: e_1_2_9_74_1
  doi: 10.1039/b401586j
– ident: e_1_2_9_31_1
  doi: 10.1021/acscatal.5b00310
– ident: e_1_2_9_39_2
  doi: 10.1002/ange.201002108
– ident: e_1_2_9_124_3
  doi: 10.1016/j.bmc.2011.06.056
– ident: e_1_2_9_3_10
  doi: 10.1039/c3np70071b
– ident: e_1_2_9_139_2
  doi: 10.1002/ange.201005741
– ident: e_1_2_9_65_1
  doi: 10.1002/cber.186900201183
– ident: e_1_2_9_95_1
  doi: 10.1021/ja304848n
– ident: e_1_2_9_60_3
  doi: 10.1002/cmdc.200700104
– ident: e_1_2_9_4_6
  doi: 10.1002/9781118690659
– ident: e_1_2_9_16_1
  doi: 10.1021/ja0516054
– ident: e_1_2_9_10_1
  doi: 10.1002/cber.19200531110
– ident: e_1_2_9_45_2
  doi: 10.1002/ange.200805652
– ident: e_1_2_9_45_3
  doi: 10.1039/c2cc17871k
– ident: e_1_2_9_71_4
  doi: 10.1002/ange.200500368
– ident: e_1_2_9_63_1
  doi: 10.1016/j.tet.2012.06.003
– ident: e_1_2_9_112_1
  doi: 10.1021/ol402701x
– ident: e_1_2_9_60_2
  doi: 10.1111/j.1749-6632.2001.tb04036.x
– ident: e_1_2_9_127_1
  doi: 10.1021/ol9000922
– ident: e_1_2_9_79_1
  doi: 10.1002/ejoc.200800394
– ident: e_1_2_9_109_1
  doi: 10.1055/s-0035-1560397
– ident: e_1_2_9_4_4
  doi: 10.1002/ange.200804497
– ident: e_1_2_9_71_1
  doi: 10.1002/anie.200201617
– ident: e_1_2_9_3_6
  doi: 10.1021/cr0505268
– ident: e_1_2_9_129_2
  doi: 10.1021/jm2013979
– ident: e_1_2_9_91_3
  doi: 10.1021/ar800138a
– volume-title: Functional Organic Materials: Syntheses, Strategies and Applications
  year: 2007
  ident: e_1_2_9_3_7
  contributor:
    fullname: Muller T. J. J.
– ident: e_1_2_9_67_1
  doi: 10.1016/j.tetlet.2009.12.138
– ident: e_1_2_9_118_1
  doi: 10.1016/j.tet.2010.01.026
– ident: e_1_2_9_12_1
  doi: 10.1039/JR9290001870
– volume: 49
  start-page: 1
  year: 1997
  ident: e_1_2_9_60_1
  publication-title: Pharmacol. Rev.
  contributor:
    fullname: Zucchi R.
– ident: e_1_2_9_60_4
  doi: 10.1039/c1cs15093f
– ident: e_1_2_9_94_2
  doi: 10.1002/ange.201204275
– ident: e_1_2_9_35_1
  doi: 10.1002/anie.201109027
– ident: e_1_2_9_97_2
  doi: 10.1002/ange.201008007
– ident: e_1_2_9_132_1
  doi: 10.1002/adsc.201000180
– ident: e_1_2_9_5_2
  doi: 10.1021/ar800039x
– ident: e_1_2_9_52_3
  doi: 10.1002/ange.200605055
– ident: e_1_2_9_3_2
  doi: 10.1021/cen-v082n036.p049
– ident: e_1_2_9_27_1
  doi: 10.1039/C5SC02143J
– ident: e_1_2_9_145_1
  doi: 10.1039/C5CC05677B
– ident: e_1_2_9_81_1
  doi: 10.1002/chem.201300480
– start-page: 2785
  year: 2009
  ident: e_1_2_9_80_2
  publication-title: Synthesis
  contributor:
    fullname: Thakur K. G.
– ident: e_1_2_9_53_1
  doi: 10.1002/anie.200904916
– ident: e_1_2_9_15_1
  doi: 10.1073/pnas.0601687103
– ident: e_1_2_9_25_1
  doi: 10.1021/ol201629n
– ident: e_1_2_9_29_1
  doi: 10.1016/j.tet.2015.07.052
– ident: e_1_2_9_70_1
  doi: 10.1016/S0040-4039(00)91094-3
– ident: e_1_2_9_129_1
  doi: 10.1016/j.bmcl.2009.08.047
– ident: e_1_2_9_32_1
  doi: 10.1021/acs.joc.5b01935
– ident: e_1_2_9_117_1
  doi: 10.1021/acs.joc.5b00888
– ident: e_1_2_9_44_2
  doi: 10.1002/ange.201101391
– ident: e_1_2_9_41_1
  doi: 10.1016/j.tet.2006.06.069
– ident: e_1_2_9_130_1
  doi: 10.1039/c3ra23230a
– ident: e_1_2_9_147_2
  doi: 10.1002/ange.201007733
– ident: e_1_2_9_69_1
  doi: 10.1016/j.tet.2014.02.022
– ident: e_1_2_9_83_1
  doi: 10.1002/aoc.3291
– ident: e_1_2_9_19_1
  doi: 10.1039/c4gc00038b
– ident: e_1_2_9_28_1
  doi: 10.1021/acs.joc.5b00800
– ident: e_1_2_9_124_1
  doi: 10.1021/jm8007823
– volume-title: The Logic of Chemical Synthesis
  year: 1995
  ident: e_1_2_9_2_1
  contributor:
    fullname: Corey E. J.
– ident: e_1_2_9_3_4
  doi: 10.1002/anie.200500368
– ident: e_1_2_9_99_1
  doi: 10.1021/acs.orglett.5b01612
– ident: e_1_2_9_120_1
  doi: 10.1016/0040-4039(93)89005-B
– ident: e_1_2_9_136_1
  doi: 10.1055/s-0029-1217822
– ident: e_1_2_9_143_1
  doi: 10.1002/chem.201102710
– ident: e_1_2_9_13_2
  doi: 10.1021/ja050058j
– ident: e_1_2_9_64_1
  doi: 10.1039/c2cc33203e
– ident: e_1_2_9_116_1
  doi: 10.1021/np0605586
– ident: e_1_2_9_134_1
  doi: 10.1002/adsc.201000062
– ident: e_1_2_9_37_1
  doi: 10.1016/j.tet.2015.07.004
– volume-title: Organic Synthesis Using Transition Metals
  year: 2012
  ident: e_1_2_9_2_2
– ident: e_1_2_9_101_2
  doi: 10.1039/C4QO00331D
– ident: e_1_2_9_49_1
  doi: 10.1002/anie.200604494
– ident: e_1_2_9_69_2
  doi: 10.1002/ejoc.201402416
– ident: e_1_2_9_97_1
  doi: 10.1002/anie.201008007
– ident: e_1_2_9_76_1
  doi: 10.1039/C4CY00868E
– ident: e_1_2_9_87_2
  doi: 10.2174/138527212800564358
– ident: e_1_2_9_23_1
  doi: 10.1002/chem.201402114
– ident: e_1_2_9_121_1
  doi: 10.1002/adsc.201300459
– ident: e_1_2_9_140_1
  doi: 10.1021/ja3004792
– ident: e_1_2_9_6_1
– volume: 52
  start-page: 1746
  year: 1919
  ident: e_1_2_9_9_1
  publication-title: Ber. Dtsch. Chem. Ges.
  contributor:
    fullname: Rosenmund K. W.
– ident: e_1_2_9_53_2
  doi: 10.1002/ange.200904916
– volume-title: Nickel‐Catalyzed Cross‐Coupling Reactions
  year: 2005
  ident: e_1_2_9_89_1
  contributor:
    fullname: Tamaru Y.
– ident: e_1_2_9_38_1
  doi: 10.1016/j.tet.2015.12.012
– ident: e_1_2_9_44_1
  doi: 10.1002/anie.201101391
– ident: e_1_2_9_17_1
  doi: 10.1016/j.tetasy.2006.02.007
– ident: e_1_2_9_91_2
  doi: 10.1002/ange.200603451
– ident: e_1_2_9_43_1
  doi: 10.1039/c4cc00637b
– ident: e_1_2_9_62_1
  doi: 10.1016/j.tet.2015.05.017
– ident: e_1_2_9_119_1
  doi: 10.1039/C0OB00622J
– ident: e_1_2_9_85_1
  doi: 10.1039/c2cc31577g
– ident: e_1_2_9_33_1
  doi: 10.1039/c2cc34659a
– ident: e_1_2_9_54_1
  doi: 10.1039/c3ra41000e
– ident: e_1_2_9_22_1
  doi: 10.1021/ja056541b
– ident: e_1_2_9_113_1
  doi: 10.1021/ol501140p
– ident: e_1_2_9_21_1
  doi: 10.1016/j.tetlet.2013.02.007
– ident: e_1_2_9_47_1
  doi: 10.1002/ejoc.201403274
– ident: e_1_2_9_78_2
  doi: 10.1002/aoc.3361
– ident: e_1_2_9_15_2
  doi: 10.1021/ar800164n
– volume: 2
  start-page: 819
  year: 1957
  ident: e_1_2_9_66_2
  publication-title: Ann. Chim. (Paris)
  contributor:
    fullname: Chodkiewicz W.
– ident: e_1_2_9_144_1
  doi: 10.1021/ol400692b
SSID ssj0009661
Score 2.4850762
Snippet Copper‐catalyzed cross‐coupling reactions have found widespread application in carbon–carbon or carbon–heteroatom bond formation. The relatively low toxicity,...
Copper-catalyzed cross-coupling reactions have found widespread application in carbon-carbon or carbon-heteroatom bond formation. The relatively low toxicity,...
SourceID hal
proquest
crossref
wiley
SourceType Open Access Repository
Aggregation Database
Publisher
StartPage 209
SubjectTerms Carbon
Chemical Sciences
Copper
C–C coupling
Decarboxylative coupling
Dehydrogenative coupling
Domino reactions
Organic chemistry
Synthetic methods
Title Emergence of Copper‐Mediated Formation of C–C Bonds
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fejoc.201600540
https://www.proquest.com/docview/1859418633
https://hal.science/hal-01601331
Volume 2017
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1LS8NAEF60F734FqNVggie0uaxyTbHEltKsQpiobew2Qei0JY-PHjqTxD8h_0lzmyaPrwIetxkl2xmd2e-WWa-IeQGbLCINKyAGynhUM1AD7KQOSqUfpDpmqAc7zs6D1GrS9u9sLeWxZ_zQywv3PBkGH2NB5xn4-qKNFS9DpCC0IsM6gAl7AUMY7runlb8UYDljcdFA-oAUukVrI2uX90cvmGVtl8wJnINcK7DVmN3mvuEFzPOw03eKtNJVhEfP8gc__NLB2RvAUrter6LDsmW6h-RnaSoBXdMWGORpansgbaTwXCoRvPZZ8fU-VDSbhYpkOb1fPaV2FiveHxCus3Gc9JyFiUXHBHERiODKQtF6GdM6hqPJTgQkoNJ5zAj8GcVy7QMqfZEhLfJCtqMZTF3ucwiX8vglJT6g746I3YUM1cgO10gBQ1DVaOYtqsDyiKOJDIWuS1Eng5zZo0051D2UxREuhSERa5hRZadkBC7Vb9P8Rl2AS_be_csUi4WLF0cw3EKYCSmHkwhsIhvJP_Lp9JG-zFZts7_MuiC7Ppo-l0MFSyT0mQ0VZcAXCbZldmc3w_K4io
link.rule.ids 230,315,783,787,888,1378,27938,27939,46308,46732
linkProvider Wiley-Blackwell
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1LS8NAEB58HPTiW6zPIIKnaB6bbHOU2FJrqyAK3pZkH4hCW_rw4MmfIPgP_SXObJpqvQh63GSXbGZ3dr4dZr4BOEIbLGODK-DFWrrMcDwHecRdHakgzE1Vsoz8He2ruHHHmvdRGU1IuTAFP8TE4UaaYc9rUnBySJ9-sYbqxy5xEPqxhR2zMI86H1IRg_ObLwYpRPP2zsVC5iJWuS95G73gdHr8lF2afaCoyG-Q8ztwtZanvgx5Oeci4OTpZDTMT-TLDzrHf_3UCiyNcalzVmykVZjRnTVYSMtycOvAa-NETe10jZN2ez3d_3h9a9tSH1o59TIL0r7-eH1PHSpZPNiAu3rtNm2446oLrgwTeyijNYtkFORcmWqWKLxDqAyteoYzwiut5rlRETO-jMmhrLHNeZ5kXqbyODAq3IS5Trejt8CJE-5JIqgLlWRRpKuMMndNyHicEY9MBY5LmYteQa4hChrlQJAgxEQQFTjEJZl0Ik7sxllL0DPqghdt_9mvwG65YmKsiQOBeCRhPk4hrEBgRf_Lp0SteZ1OWtt_GXQAC43bdku0Lq4ud2AxICTgUeTgLswN-yO9hzhmmO_bnfoJSHTmRA
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1LS8NAEB58gHrxLVarBhE8peax2W2OJW2pbxELvS3JPhCFttTqwZM_QfAf9pe4s2lq9SLocZNdspl9zDfDzDcAR0YHC6rNCnhUCZdoZu5BFjFXRTIIM10VJEV_x-UVbbXJWSfqTGXx5_wQE4cbngx7X-MB70t98kUaqh56SEHoU4s6ZmGe0NDDoK767ReBlAHz1uQiIXENVOkUtI1ecPJ9_De1NHuPQZFTiHMat1rF01yBtJhyHm_yWHkeZhXx-oPN8T__tArLY1Tq1PJttAYzqrsOi0lRDG4DWGOcpqmcnnaSXr-vBqO390tb6ENJp1nkQNrXo7ePxMGCxU-b0G427pKWO6654Iowtley0WWRiIKMSV1NY2ksCJkanZ6aGRmDVrFMy4hoX1B0JyvTZiyLUy-VGQ20DLdgrtvrqm1waMw8gfR0oRQkilSVYN6uDgmjKbLIlOC4EDnv59QaPCdRDjgKgk8EUYJDsyKTTsiI3apdcHyGXYyZ7b_4JSgXC8bH5_CJGzQSE99MISxBYCX_y6d44-w6mbR2_jLoABZu6k1-cXp1vgtLAcIAD8MGyzA3HDyrPQNihtm-3aefoADk8w
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=Emergence+of+Copper%E2%80%90Mediated+Formation+of+C%E2%80%93C+Bonds&rft.jtitle=European+journal+of+organic+chemistry&rft.au=Maaliki%2C+Carine&rft.au=Thiery%2C+Emilie&rft.au=Thibonnet%2C+J%C3%A9r%C3%B4me&rft.date=2017-01-10&rft.issn=1434-193X&rft.eissn=1099-0690&rft.volume=2017&rft.issue=2&rft.spage=209&rft.epage=228&rft_id=info:doi/10.1002%2Fejoc.201600540&rft.externalDBID=10.1002%252Fejoc.201600540&rft.externalDocID=EJOC201600540
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1434-193X&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1434-193X&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1434-193X&client=summon