A palladium-catalyzed sequential Heck coupling/C-C bond activation approach to oxindoles with all-carbon-quaternary centers

Catalytic construction of oxindoles bearing all-carbon-quaternary centers attracts wide attention from the synthetic chemistry community. Herein, we report a palladium-catalyzed sequential Heck coupling/C-C bond activation of aryl halide-tethered alkenes with benzocyclobutenols affording a series of...

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Published inOrganic & biomolecular chemistry Vol. 2; no. 8; pp. 1642 - 1646
Main Authors Mao, Guoliang, Meng, Chenxiang, Cheng, Fangyuan, Wu, Wenbo, Gao, Yuan-Yuan, Li, Gao-Wei, Liu, Lantao
Format Journal Article
LanguageEnglish
Published CAMBRIDGE Royal Soc Chemistry 23.02.2022
Royal Society of Chemistry
Subjects
Alkenes
Carbon
Chemistry
Chemistry, Organic
Coupling
Covalent bonds
Enantiomers
Palladium
Physical Sciences
Science & Technology
FUNCTIONALIZATION
INSERTION
ASYMMETRIC-SYNTHESIS
RING-FUSED BENZOCYCLOBUTENOLS
CONSTRUCTION
SITE-SELECTIVITY
PHYSOSTIGMINE
CLEAVAGE
ENANTIOMER
H ACTIVATION
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Abstract Catalytic construction of oxindoles bearing all-carbon-quaternary centers attracts wide attention from the synthetic chemistry community. Herein, we report a palladium-catalyzed sequential Heck coupling/C-C bond activation of aryl halide-tethered alkenes with benzocyclobutenols affording a series of oxindole-derived compounds in good to excellent yields, as well as the preliminary enantioselectivity results. Catalytic construction of oxindoles bearing all-carbon-quaternary centers attracts wide attention from the synthetic chemistry community.
AbstractList Catalytic construction of oxindoles bearing all-carbon-quaternary centers attracts wide attention from the synthetic chemistry community. Herein, we report a palladium-catalyzed sequential Heck coupling/C–C bond activation of aryl halide-tethered alkenes with benzocyclobutenols affording a series of oxindole-derived compounds in good to excellent yields, as well as the preliminary enantioselectivity results.
Catalytic construction of oxindoles bearing all-carbon-quaternary centers attracts wide attention from the synthetic chemistry community. Herein, we report a palladium-catalyzed sequential Heck coupling/C-C bond activation of aryl halide-tethered alkenes with benzocyclobutenols affording a series of oxindole-derived compounds in good to excellent yields, as well as the preliminary enantioselectivity results. Catalytic construction of oxindoles bearing all-carbon-quaternary centers attracts wide attention from the synthetic chemistry community.
Author Gao, Yuan-Yuan
Mao, Guoliang
Liu, Lantao
Wu, Wenbo
Meng, Chenxiang
Cheng, Fangyuan
Li, Gao-Wei
AuthorAffiliation College of Chemistry
Provincial Key Laboratory of Oil and Gas Chemical Technology
Henan Engineering Laboratory of Green Synthesis for Pharmaceuticals
Shangqiu Normal University
College of Chemistry and Chemical Engineering
Northeast Petroleum University
Zhengzhou University
AuthorAffiliation_xml – name: Provincial Key Laboratory of Oil and Gas Chemical Technology
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CitedBy_id crossref_primary_10_1021_acs_orglett_3c01788
crossref_primary_10_1002_slct_202300153
crossref_primary_10_1039_D2QO00655C
crossref_primary_10_1002_aoc_6988
Cites_doi 10.1021/acs.orglett.5b03518
10.1021/ol1012668
10.1021/acs.chemrev.6b00599
10.1021/acs.orglett.9b02788
10.1002/chem.200601016
10.1021/jm051122a
10.1002/anie.201101053
10.1021/ja407422q
10.1002/adsc.201901100
10.1021/jacs.8b08190
10.1002/anie.200703408
10.1016/j.jorganchem.2019.120963
10.1002/anie.201209475
10.1039/c4cc07667b
10.1002/anie.201706325
10.1021/acscatal.6b03210
10.1021/acs.orglett.1c03739
10.1002/anie.201704922
10.1021/jacs.6b01656
10.1021/ja500118w
10.1002/anie.200805652
10.1021/acs.orglett.7b03713
10.1002/anie.201800330
10.1016/j.ejmech.2016.08.011
10.1039/b904405a
10.1039/c0cc02566f
10.1039/c4qo00053f
10.1126/science.1193225
10.1021/acs.chemrev.0c00167
10.1021/acs.orglett.0c00999
10.1021/acs.chemrev.0c00346
10.1016/j.gresc.2021.10.006
10.1021/ja901018g
10.1055/s-0036-1590830
10.1021/acs.accounts.0c00297
10.1021/ja512212x
10.1002/anie.201405067
10.1002/anie.201509973
10.1002/anie.202102769
10.1002/ejoc.201100836
10.1021/acs.chemrev.0c00569
10.1021/jacs.1c03827
10.1021/acs.chemrev.0c00166
10.1002/ejoc.201501291
10.1021/acs.chemrev.0c00151
10.1002/anie.200701342
10.1021/ol200149s
10.1021/jo201632c
10.1002/anie.200800549
10.1039/c8cs00386f
10.1039/c4cc09327e
10.1021/jacs.9b12698
10.1002/ejic.200200535
10.1021/ja807129e
10.1039/c6cc04359c
10.1002/chem.201603382
10.1002/anie.201306532
10.1039/d1qo00186h
10.1002/anie.201606955
10.1021/jacs.5b11625
10.1021/acs.chemrev.0c00109
10.1002/ejoc.201101616
10.1055/s-2006-926302
10.1039/b308864m
10.1021/ja309013a
10.1021/acscatal.9b03172
10.1039/c6ob00554c
10.1002/ejoc.200300050
10.1021/acs.chemrev.5b00138
10.1039/b903516h
10.1021/acscatal.1c02277
10.1055/s-0029-1216975
10.1055/s-0030-1260233
10.1021/ol403021p
10.1021/acs.joc.7b01727
10.1021/acs.orglett.8b03653
10.1002/anie.201603950
10.1039/C4QO00053F
10.1039/C8CS00386F
10.1039/C6OB00554C
10.2174/138527207782418645
10.1039/D1QO00186H
10.1039/B308864M
10.1016/S0031-9422(97)00946-1
10.1055/s-1995-5286
10.1039/C0CC02566F
10.1039/C4CC07667B
10.1039/C4CC09327E
10.1021/jo00077a005
10.1021/ja980788+
10.1039/C6CC04359C
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Issue 8
Keywords FUNCTIONALIZATION
INSERTION
ASYMMETRIC-SYNTHESIS
RING-FUSED BENZOCYCLOBUTENOLS
CONSTRUCTION
SITE-SELECTIVITY
PHYSOSTIGMINE
CLEAVAGE
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Royal Society of Chemistry
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References Trost, BM (WOS:000235146000001) 2006
Sivaguru, P (WOS:000468628400004) 2019; 48
Pinto, A (WOS:000243622500026) 2007; 13
Cao, KN (WOS:000744124300035) 2021; 23
Li, CC (WOS:000376111000002) 2016; 14
Xia, Y (WOS:000332144300021) 2014; 136
Fumagalli, G (WOS:000405642800022) 2017; 117
Ruhland, K (WOS:000303440000002) 2012; 2012
Aïssa, C (WOS:000296195400001) 2011
He, YY (WOS:000455285800040) 2019; 21
Chen, PH (WOS:000390600900001) 2016; 22
Murakami, M (WOS:000611061700008) 2021; 121
Ding, LN (WOS:000329586600038) 2014; 136
Klein, JEMN (WOS:000297205800001) 2011; 2011
Jun, CH (WOS:000225975600006) 2004; 33
Seiser, T (WOS:000267728400001) 2009; 7
Pan, Q (WOS:000674321800028) 2021; 143
Murakami, M (WOS:000386540500001) 2016; 138
Marti, C (WOS:000183839800003) 2003; 2003
Perry, A (WOS:000266555300031) 2009
Marek, I (WOS:000347238800004) 2015; 54
Vicente, R (WOS:000611061700006) 2021; 121
Chen, PH (WOS:000393539200047) 2017; 7
Kong, WQ (WOS:000367636600013) 2015; 137
Li, YM (WOS:000316915500029) 2013; 52
Liu, C (WOS:000329077700015) 2013; 15
Matsuura, T (WOS:000074727600009) 1998; 120
Kündig, EP (WOS:000250990000035) 2007; 46
Kong, WQ (WOS:000383372700047) 2016; 55
Wang, K (WOS:000446920100013) 2018; 140
Ma, T (WOS:000489204000031) 2019; 9
Wang, M (WOS:000348690100046) 2015; 137
Desrosiers, JN (WOS:000384713100038) 2016; 55
Liu, LT (WOS:000674927200050) 2021; 11
Wasa, M (WOS:000260301700019) 2008; 130
Yoon, H (WOS:000408267000056) 2017; 56
Liang, RX (WOS:000526894000070) 2020; 22
McDonald, TR (WOS:000611061700002) 2021; 121
Chuang, C.-P. (000749767200001.35) 2017
Faissner, R (WOS:000184022400003) 2003
Ruck, RT (WOS:000256894600019) 2008; 47
Galliford, CV (WOS:000251354300003) 2007; 46
Chen, XW (WOS:000649233500001) 2021; 60
Li, SL (WOS:001022602900001) 2021; 2
Würtz, S (WOS:000267630000004) 2009; 131
Liu, LT (WOS:000288691600023) 2011; 13
Seiser, T (WOS:000294175700004) 2011; 50
Murakami, M (WOS:000286055700001) 2011; 47
Kondo, T (WOS:000372848000001) 2016; 2016
Jang, YJ (WOS:000410810600046) 2017; 56
Sokolova, OO (WOS:000611061700003) 2021; 121
Shaw, MH (WOS:000382673600001) 2016; 52
Klein, JEMN (WOS:000280398900042) 2010; 12
Trost, BM (WOS:000270506800001) 2009
Piou, T (WOS:000326807900037) 2013; 52
Anderton, N (WOS:000074422400006) 1998; 48
Lu, AL (WOS:000426759900041) 2018; 57
Yu, JJ (WOS:000368070000055) 2016; 55
Pirenne, V (WOS:000611061700007) 2021; 121
Ishida, N (WOS:000348213200025) 2015; 51
Dermenci, A (WOS:000364426500018) 2014; 1
Marchese, AD (WOS:000563017200018) 2020; 53
Li, J (WOS:000344596700032) 2014; 50
Ishida, N (WOS:000310103800044) 2012; 134
ASHIMORI, A (WOS:A1993ML30700005) 1993; 58
Jia, YX (WOS:000263642300022) 2009; 48
Rottmann, M (WOS:000281485600027) 2010; 329
Lu, GZ (WOS:000494688800014) 2019; 361
Kaur, M (WOS:000385319000069) 2016; 123
Kong, LY (WOS:000507144400017) 2020; 142
Li, YX (WOS:000426013600007) 2018; 20
Chtchemelinine, A (WOS:000296206400062) 2011; 76
Zhao, CL (WOS:000368563200046) 2016; 18
Xu, S (WOS:000487577200065) 2019; 21
Necas, D (WOS:000251207500006) 2007; 11
KRAUS, GA (WOS:A1995RD26100023) 1995
Ramesh, K (WOS:000493061500006) 2019; 902
Souillart, L (WOS:000361254500012) 2015; 115
Mao, WB (WOS:000427996900008) 2018; 29
Cohen, Y (WOS:000611061700005) 2021; 121
Ding, K (WOS:000238114700001) 2006; 49
Mao, WB (WOS:000410004800035) 2017; 82
Chen, JF (WOS:000635210500001) 2021; 8
Seiser (D1OB02440J/cit17c/1) 2009; 7
Matsuura (D1OB02440J/cit12b/1) 1998; 120
He (D1OB02440J/cit19f/1) 2019; 21
Wang (D1OB02440J/cit12f/1) 2015; 137
Trost (D1OB02440J/cit2b/1) 2006; 37
Chen (D1OB02440J/cit7b/1) 2021; 8
Li (D1OB02440J/cit11a/1) 2014; 50
Kraus (D1OB02440J/cit18b/1) 1995
Ishida (D1OB02440J/cit19a/1) 2012; 134
Marti (D1OB02440J/cit2a/1) 2003
Chtchemelinine (D1OB02440J/cit21a/1) 2011; 76
Li (D1OB02440J/cit8a/1) 2018; 20
Jia (D1OB02440J/cit5a/1) 2009; 48
Souillart (D1OB02440J/cit15b/1) 2015; 115
Rottmann (D1OB02440J/cit2d/1) 2010; 329
Aïssa (D1OB02440J/cit17e/1) 2011
Ding (D1OB02440J/cit18a/1) 2014; 136
Galliford (D1OB02440J/cit1d/1) 2007; 46
Yoon (D1OB02440J/cit12g/1) 2017; 56
Klein (D1OB02440J/cit5c/1) 2010; 12
Liu (D1OB02440J/cit6c/1) 2011; 13
Kaur (D1OB02440J/cit1e/1) 2016; 123
Ruhland (D1OB02440J/cit16b/1) 2012
Chen (D1OB02440J/cit17h/1) 2017; 7
Ruck (D1OB02440J/cit12d/1) 2008; 47
Liang (D1OB02440J/cit7a/1) 2020; 22
Mao (D1OB02440J/cit21b/1) 2017; 82
Kong (D1OB02440J/cit6e/1) 2020; 142
Liu (D1OB02440J/cit9/1) 2013; 15
Wasa (D1OB02440J/cit4/1) 2008; 130
Ashimori (D1OB02440J/cit12a/1) 1993; 58
Sokolova (D1OB02440J/cit17k/1) 2021; 121
Perry (D1OB02440J/cit5b/1) 2009; 44
Chen (D1OB02440J/cit8e/1) 2021; 60
Necas (D1OB02440J/cit17b/1) 2007; 11
Liu (D1OB02440J/cit22/1) 2021; 11
Ding (D1OB02440J/cit1c/1) 2006; 49
Murakami (D1OB02440J/cit15c/1) 2016; 138
Chuang (D1OB02440J/cit11b/1) 2017
Dermenci (D1OB02440J/cit15a/1) 2014; 1
Ramesh (D1OB02440J/cit12i/1) 2019; 902
Mao (D1OB02440J/cit19e/1) 2018
Pirenne (D1OB02440J/cit17n/1) 2021; 121
Ishida (D1OB02440J/cit19c/1) 2015; 51
Jang (D1OB02440J/cit14/1) 2017; 56
Anderton (D1OB02440J/cit1a/1) 1998; 48
Wang (D1OB02440J/cit8b/1) 2018; 140
Sivaguru (D1OB02440J/cit17i/1) 2019; 48
Kündig (D1OB02440J/cit6a/1) 2007; 46
Zhao (D1OB02440J/cit19d/1) 2016; 18
Xu (D1OB02440J/cit8d/1) 2019; 21
Li (D1OB02440J/cit10/1) 2013; 52
McDonald (D1OB02440J/cit17j/1) 2021; 121
Li (D1OB02440J/cit3c/1) 2016; 14
Würtz (D1OB02440J/cit6b/1) 2009; 131
Murakami (D1OB02440J/cit17o/1) 2021; 121
Lu (D1OB02440J/cit12h/1) 2018; 57
Marek (D1OB02440J/cit16c/1) 2015; 54
Seiser (D1OB02440J/cit17d/1) 2011; 50
Kong (D1OB02440J/cit6d/1) 2015; 137
Klein (D1OB02440J/cit3a/1) 2011
Trost (D1OB02440J/cit2c/1) 2009
Vicente (D1OB02440J/cit17m/1) 2021; 121
Ma (D1OB02440J/cit8c/1) 2019; 9
Piou (D1OB02440J/cit12e/1) 2013; 52
Yu (D1OB02440J/cit20/1) 2016; 55
Kong (D1OB02440J/cit2e/1) 2016; 55
Marchese (D1OB02440J/cit3b/1) 2020; 53
Fumagalli (D1OB02440J/cit15e/1) 2017; 117
Cohen (D1OB02440J/cit17l/1) 2021; 121
Li (D1OB02440J/cit15f/1) 2021; 2
Pinto (D1OB02440J/cit12c/1) 2007; 13
Desrosiers (D1OB02440J/cit13/1) 2016; 55
Shaw (D1OB02440J/cit15d/1) 2016; 52
Xia (D1OB02440J/cit19b/1) 2014; 136
Chen (D1OB02440J/cit17g/1) 2016; 22
Lu (D1OB02440J/cit6f/1) 2019; 361
Murakami (D1OB02440J/cit16a/1) 2011; 47
Pan (D1OB02440J/cit8f/1) 2021; 143
Cao (D1OB02440J/cit17p/1) 2021; 23
Faissner (D1OB02440J/cit1b/1) 2003; 2003
Jun (D1OB02440J/cit17a/1) 2004; 33
Kondo (D1OB02440J/cit17f/1) 2016
References_xml – volume: 18
  start-page: 328
  year: 2016
  ident: WOS:000368563200046
  article-title: Rh(I)-Catalyzed Insertion of Allenes into C-C Bonds of Benzocyclobutenols
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.5b03518
  contributor:
    fullname: Zhao, CL
– volume: 12
  start-page: 3446
  year: 2010
  ident: WOS:000280398900042
  article-title: First C-H Activation Route to Oxindoles using Copper Catalysis
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol1012668
  contributor:
    fullname: Klein, JEMN
– volume: 117
  start-page: 9404
  year: 2017
  ident: WOS:000405642800022
  article-title: Recent Methodologies That Exploit C-C Single-Bond Cleavage of Strained Ring Systems by Transition Metal Complexes
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/acs.chemrev.6b00599
  contributor:
    fullname: Fumagalli, G
– volume: 21
  start-page: 7498
  year: 2019
  ident: WOS:000487577200065
  article-title: Ni-Catalyzed Reductive Arylacylation of Alkenes toward Carbonyl-Containing Oxindoles
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.9b02788
  contributor:
    fullname: Xu, S
– volume: 13
  start-page: 961
  year: 2007
  ident: WOS:000243622500026
  article-title: Palladium-catalyzed enantioselective domino Heck-cyanation sequence: Development and application to the total synthesis of esermethole and physostigmine
  publication-title: CHEMISTRY-A EUROPEAN JOURNAL
  doi: 10.1002/chem.200601016
  contributor:
    fullname: Pinto, A
– volume: 49
  start-page: 3432
  year: 2006
  ident: WOS:000238114700001
  article-title: Structure-based design of spiro-oxindoles as potent, specific small-molecule inhibitors of the MDM2-p53 interaction
  publication-title: JOURNAL OF MEDICINAL CHEMISTRY
  doi: 10.1021/jm051122a
  contributor:
    fullname: Ding, K
– start-page: 541
  year: 1995
  ident: WOS:A1995RD26100023
  article-title: DIRECT SYNTHESIS OF THE DIMETHYL ETHER OF BENZO[A]NAPHTHACENEQUINONE G-2N
  publication-title: SYNLETT
  contributor:
    fullname: KRAUS, GA
– volume: 50
  start-page: 7740
  year: 2011
  ident: WOS:000294175700004
  article-title: Cyclobutanes in Catalysis
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201101053
  contributor:
    fullname: Seiser, T
– volume: 136
  start-page: 169
  year: 2014
  ident: WOS:000329586600038
  article-title: sp3-sp2 vs sp3-sp3 C-C Site Selectivity in Rh-Catalyzed Ring Opening of Benzocyclobutenol: A DFT Study
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja407422q
  contributor:
    fullname: Ding, LN
– volume: 361
  start-page: 4961
  year: 2019
  ident: WOS:000494688800014
  article-title: Palladium-Catalyzed Domino Heck/Phosphorylation towards 3,3-Disubstituted Phosphinonyloxindoles
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201901100
  contributor:
    fullname: Lu, GZ
– volume: 140
  start-page: 12364
  year: 2018
  ident: WOS:000446920100013
  article-title: Ni-Catalyzed Enantioselective Reductive Diarylation of Activated Alkenes by Domino Cyclization/Cross-Coupling
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.8b08190
  contributor:
    fullname: Wang, K
– volume: 46
  start-page: 8484
  year: 2007
  ident: WOS:000250990000035
  article-title: Bulky chiral carbene ligands and their application in the palladium-catalyzed asymmetric intramolecular α-arylation of amides
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.200703408
  contributor:
    fullname: Kündig, EP
– volume: 902
  start-page: ARTN 120963
  year: 2019
  ident: WOS:000493061500006
  article-title: Microwave-assisted intramolecular reductive Heck in aqueous medium: Synthesis of 3,3′-Disubstituted heterocyclic compounds
  publication-title: JOURNAL OF ORGANOMETALLIC CHEMISTRY
  doi: 10.1016/j.jorganchem.2019.120963
  contributor:
    fullname: Ramesh, K
– volume: 52
  start-page: 3972
  year: 2013
  ident: WOS:000316915500029
  article-title: Direct Annulations toward Phosphorylated Oxindoles: Silver-Catalyzed Carbon-Phosphorus Functionalization of Alkenes
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201209475
  contributor:
    fullname: Li, YM
– volume: 50
  start-page: 15049
  year: 2014
  ident: WOS:000344596700032
  article-title: Radical cascade cyanomethylation of activated alkenes to construct cyano substituted oxindoles
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c4cc07667b
  contributor:
    fullname: Li, J
– volume: 56
  start-page: 10920
  year: 2017
  ident: WOS:000408267000056
  article-title: Palladium-Catalyzed Spirocyclization through C-H Activation and Regioselective Alkyne Insertion
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201706325
  contributor:
    fullname: Yoon, H
– volume: 7
  start-page: 1340
  year: 2017
  ident: WOS:000393539200047
  article-title: "Cut and Sew" Transformations via Transition-Metal-Catalyzed Carbon-Carbon Bond Activation
  publication-title: ACS CATALYSIS
  doi: 10.1021/acscatal.6b03210
  contributor:
    fullname: Chen, PH
– volume: 23
  start-page: 9520
  year: 2021
  ident: WOS:000744124300035
  article-title: Palladium-Catalyzed Asymmetric Cross-Coupling Reactions of Cyclobutanols and Unactivated Olefins
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.1c03739
  contributor:
    fullname: Cao, KN
– volume: 56
  start-page: 11927
  year: 2017
  ident: WOS:000410810600046
  article-title: Rhodium-Catalyzed Enantioselective Reductive Arylation: Convenient Access to 3,3-Disubstituted Oxindoles
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201704922
  contributor:
    fullname: Jang, YJ
– volume: 138
  start-page: 13759
  year: 2016
  ident: WOS:000386540500001
  article-title: Potential of Metal-Catalyzed C-C Single Bond Cleavage for Organic Synthesis
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.6b01656
  contributor:
    fullname: Murakami, M
– volume: 136
  start-page: 3013
  year: 2014
  ident: WOS:000332144300021
  article-title: Formal Carbene Insertion into C-C Bond: Rh(I)-Catalyzed Reaction of Benzocyclobutenols with Diazoesters
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja500118w
  contributor:
    fullname: Xia, Y
– volume: 48
  start-page: 1636
  year: 2009
  ident: WOS:000263642300022
  article-title: Oxindole Synthesis by Direct Coupling of Csp2-H and Csp3-H Centers
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.200805652
  contributor:
    fullname: Jia, YX
– volume: 20
  start-page: 921
  year: 2018
  ident: WOS:000426013600007
  article-title: Nickel-Catalyzed Domino Heck Cyclization/Suzuki Coupling for the Synthesis of 3,3-Disubstituted Oxindoles
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.7b03713
  contributor:
    fullname: Li, YX
– volume: 57
  start-page: 3233
  year: 2018
  ident: WOS:000426759900041
  article-title: Palladium-Catalyzed C-H Silylation through Palladacycles Generated from Aryl Halides
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201800330
  contributor:
    fullname: Lu, AL
– volume: 123
  start-page: 858
  year: 2016
  ident: WOS:000385319000069
  article-title: Oxindole: A chemical prism carrying plethora of therapeutic benefits
  publication-title: EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
  doi: 10.1016/j.ejmech.2016.08.011
  contributor:
    fullname: Kaur, M
– start-page: 1273
  year: 2017
  ident: 000749767200001.35
  publication-title: Synthesis
  contributor:
    fullname: Chuang, C.-P.
– volume: 7
  start-page: 2835
  year: 2009
  ident: WOS:000267728400001
  article-title: Enantioselective metal-catalyzed activation of strained rings
  publication-title: ORGANIC & BIOMOLECULAR CHEMISTRY
  doi: 10.1039/b904405a
  contributor:
    fullname: Seiser, T
– volume: 47
  start-page: 1100
  year: 2011
  ident: WOS:000286055700001
  article-title: Metal-catalysed cleavage of carbon-carbon bonds
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c0cc02566f
  contributor:
    fullname: Murakami, M
– volume: 1
  start-page: 567
  year: 2014
  ident: WOS:000364426500018
  article-title: Direct activation of relatively unstrained carbon-carbon bonds in homogeneous systems
  publication-title: ORGANIC CHEMISTRY FRONTIERS
  doi: 10.1039/c4qo00053f
  contributor:
    fullname: Dermenci, A
– volume: 329
  start-page: 1175
  year: 2010
  ident: WOS:000281485600027
  article-title: Spiroindolones, a Potent Compound Class for the Treatment of Malaria
  publication-title: SCIENCE
  doi: 10.1126/science.1193225
  contributor:
    fullname: Rottmann, M
– volume: 121
  start-page: 140
  year: 2021
  ident: WOS:000611061700005
  article-title: Creating Stereocenters within Acyclic Systems by C-C Bond Cleavage of Cyclopropanes
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/acs.chemrev.0c00167
  contributor:
    fullname: Cohen, Y
– volume: 22
  start-page: 3215
  year: 2020
  ident: WOS:000526894000070
  article-title: 3,3′-Disubstituted Oxindoles Formation via Copper-Catalyzed Arylboration and Arylsilylation of Alkenes
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.0c00999
  contributor:
    fullname: Liang, RX
– volume: 121
  start-page: 3
  year: 2021
  ident: WOS:000611061700002
  article-title: Selective Carbon-Carbon Bond Cleavage of Cyclopropanols
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/acs.chemrev.0c00346
  contributor:
    fullname: McDonald, TR
– volume: 2
  start-page: 374
  year: 2021
  ident: WOS:001022602900001
  article-title: Pd-catalyzed enantioselective intramolecular Heck reaction to access disubstituted dihydroisoquinolinone with a terminal olefin
  publication-title: GREEN SYNTHESIS AND CATALYSIS
  doi: 10.1016/j.gresc.2021.10.006
  contributor:
    fullname: Li, SL
– volume: 11
  start-page: 1566
  year: 2007
  ident: WOS:000251207500006
  article-title: Rhodium-catalyzed C-C bond cleavage reactions
  publication-title: CURRENT ORGANIC CHEMISTRY
  contributor:
    fullname: Necas, D
– volume: 131
  start-page: 8344
  year: 2009
  ident: WOS:000267630000004
  article-title: IBiox[(-)-menthyl]: A Sterically Demanding Chiral NHC Ligand
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja901018g
  contributor:
    fullname: Würtz, S
– volume: 29
  start-page: 731
  year: 2018
  ident: WOS:000427996900008
  article-title: Rhodium-Catalyzed C-C Bond Olefination of Ring-Fused Benzocyclobutenols and Application in the Construction of Polycyclic Compounds
  publication-title: SYNLETT
  doi: 10.1055/s-0036-1590830
  contributor:
    fullname: Mao, WB
– volume: 53
  start-page: 1605
  year: 2020
  ident: WOS:000563017200018
  article-title: Metal-Catalyzed Approaches toward the Oxindole Core
  publication-title: ACCOUNTS OF CHEMICAL RESEARCH
  doi: 10.1021/acs.accounts.0c00297
  contributor:
    fullname: Marchese, AD
– volume: 137
  start-page: 1341
  year: 2015
  ident: WOS:000348690100046
  article-title: Pd-Catalyzed Intramolecular C-N Bond Cleavage, 1,4-Migration, sp3 C-H Activation, and Heck Reaction: Four Controllable Diverse Pathways Depending on the Judicious Choice of the Base and Ligand
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja512212x
  contributor:
    fullname: Wang, M
– volume: 54
  start-page: 414
  year: 2015
  ident: WOS:000347238800004
  article-title: Selective Carbon-Carbon Bond Cleavage for the Stereoselective Synthesis of Acyclic Systems
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201405067
  contributor:
    fullname: Marek, I
– volume: 55
  start-page: 1143
  year: 2016
  ident: WOS:000368070000055
  article-title: Synthesis of Multiply Substituted Polycyclic Aromatic Hydrocarbons by Iridium-Catalyzed Annulation of Ring-Fused Benzocyclobutenol with Alkyne through C-C Bond Cleavage
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201509973
  contributor:
    fullname: Yu, JJ
– volume: 60
  start-page: 14068
  year: 2021
  ident: WOS:000649233500001
  article-title: Nickel-Catalyzed Asymmetric Reductive Carbo-Carboxylation of Alkenes with CO2
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.202102769
  contributor:
    fullname: Chen, XW
– volume: 2011
  start-page: 6821
  year: 2011
  ident: WOS:000297205800001
  article-title: Transition-Metal-Mediated Routes to 3,3-Disubstituted Oxindoles through Anilide Cyclisation
  publication-title: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1002/ejoc.201100836
  contributor:
    fullname: Klein, JEMN
– volume: 121
  start-page: 264
  year: 2021
  ident: WOS:000611061700008
  article-title: Cleavage of Carbon-Carbon σ-Bonds of Four-Membered Rings
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/acs.chemrev.0c00569
  contributor:
    fullname: Murakami, M
– volume: 143
  start-page: 10282
  year: 2021
  ident: WOS:000674321800028
  article-title: Ni-Catalyzed Ligand-Controlled Regiodivergent Reductive Dicarbofunctionalization of Alkenes
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.1c03827
  contributor:
    fullname: Pan, Q
– volume: 121
  start-page: 80
  year: 2021
  ident: WOS:000611061700003
  article-title: Selective Carbon-Carbon Bond Cleavage of Cyclopropylamine Derivatives
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/acs.chemrev.0c00166
  contributor:
    fullname: Sokolova, OO
– volume: 2016
  start-page: 1232
  year: 2016
  ident: WOS:000372848000001
  article-title: Ruthenium- and Rhodium-Catalyzed Strain-Driven Cleavage and Reconstruction of the C-C Bond
  publication-title: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1002/ejoc.201501291
  contributor:
    fullname: Kondo, T
– volume: 121
  start-page: 162
  year: 2021
  ident: WOS:000611061700006
  article-title: C-C Bond Cleavages of Cyclopropenes: Operating for Selective Ring-Opening Reactions
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/acs.chemrev.0c00151
  contributor:
    fullname: Vicente, R
– volume: 46
  start-page: 8748
  year: 2007
  ident: WOS:000251354300003
  article-title: Pyrrolidinyl-spirooxindole natural products as inspirations for the development of potential therapeutic agents
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.200701342
  contributor:
    fullname: Galliford, CV
– volume: 48
  start-page: 437
  year: 1998
  ident: WOS:000074422400006
  article-title: Oxindoles from Phalaris coerulescens
  publication-title: PHYTOCHEMISTRY
  contributor:
    fullname: Anderton, N
– volume: 13
  start-page: 1666
  year: 2011
  ident: WOS:000288691600023
  article-title: Synthesis of Chiral N-Heterocyclic Carbene Ligands with Rigid Backbones and Application to the Palladium-Catalyzed Enantioselective Intramolecular α-Arylation of Amides
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol200149s
  contributor:
    fullname: Liu, LT
– volume: 76
  start-page: 9157
  year: 2011
  ident: WOS:000296206400062
  article-title: Palladium-Catalyzed Selective Carboelimination and Cross-Coupling Reactions of Benzocyclobutenols with Aryl Bromides
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/jo201632c
  contributor:
    fullname: Chtchemelinine, A
– volume: 47
  start-page: 4711
  year: 2008
  ident: WOS:000256894600019
  article-title: Palladium-catalyzed tandem Heck reaction/C-H functionalization - Preparation of spiro-indane-oxindoles
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.200800549
  contributor:
    fullname: Ruck, RT
– volume: 48
  start-page: 2615
  year: 2019
  ident: WOS:000468628400004
  article-title: Cleavage of carbon-carbon bonds by radical reactions
  publication-title: CHEMICAL SOCIETY REVIEWS
  doi: 10.1039/c8cs00386f
  contributor:
    fullname: Sivaguru, P
– volume: 51
  start-page: 1882
  year: 2015
  ident: WOS:000348213200025
  article-title: Construction of tetralin skeletons based on rhodium-catalysed site-selective ring opening of benzocyclobutenols
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c4cc09327e
  contributor:
    fullname: Ishida, N
– volume: 142
  start-page: 93
  year: 2020
  ident: WOS:000507144400017
  article-title: From Prochiral N-Heterocyclic Carbenes to Optically Pure Metal Complexes: New Opportunities in Asymmetric Catalysis
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.9b12698
  contributor:
    fullname: Kong, LY
– start-page: 2219
  year: 2003
  ident: WOS:000184022400003
  article-title: Synthesis of tripod ligands containing mixed donor sets with phosphane and pyrazole donors -: Bidentate chelate binding modes and dynamic behaviour of tripod ligands in d8-metal complexes (NiII, PdII, PtII)
  publication-title: EUROPEAN JOURNAL OF INORGANIC CHEMISTRY
  doi: 10.1002/ejic.200200535
  contributor:
    fullname: Faissner, R
– volume: 130
  start-page: 14058
  year: 2008
  ident: WOS:000260301700019
  article-title: Synthesis of β-, γ-, and δ-Lactams via Pd(II)-Catalyzed C-H Activation Reactions
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja807129e
  contributor:
    fullname: Wasa, M
– volume: 52
  start-page: 10817
  year: 2016
  ident: WOS:000382673600001
  article-title: Synthesis and applications of rhodacyclopentanones derived from C-C bond activation
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c6cc04359c
  contributor:
    fullname: Shaw, MH
– volume: 22
  start-page: 18290
  year: 2016
  ident: WOS:000390600900001
  article-title: Cyclobutenones and Benzocyclobutenones: Versatile Synthons in Organic Synthesis
  publication-title: CHEMISTRY-A EUROPEAN JOURNAL
  doi: 10.1002/chem.201603382
  contributor:
    fullname: Chen, PH
– volume: 52
  start-page: 12385
  year: 2013
  ident: WOS:000326807900037
  article-title: Palladium-Catalyzed Through-Space C(sp3)-H and C(sp2)-H Bond Activation by 1,4-Palladium Migration: Efficient Synthesis of [3,4]-Fused Oxindoles
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201306532
  contributor:
    fullname: Piou, T
– volume: 8
  start-page: 2532
  year: 2021
  ident: WOS:000635210500001
  article-title: Copper-catalyzed enantioselective arylboronation of activated alkenes leading to chiral 3,3′-disubstituted oxindoles
  publication-title: ORGANIC CHEMISTRY FRONTIERS
  doi: 10.1039/d1qo00186h
  contributor:
    fullname: Chen, JF
– volume: 55
  start-page: 11921
  year: 2016
  ident: WOS:000384713100038
  article-title: Construction of Quaternary Stereocenters by Nickel-Catalyzed Heck Cyclization Reactions
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201606955
  contributor:
    fullname: Desrosiers, JN
– volume: 137
  start-page: 16028
  year: 2015
  ident: WOS:000367636600013
  article-title: Palladium-Catalyzed Enantioselective Domino Heck/Intermolecular C-H Bond Functionalization: Development and Application to the Synthesis of (+)-Esermethole
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.5b11625
  contributor:
    fullname: Kong, WQ
– volume: 121
  start-page: 227
  year: 2021
  ident: WOS:000611061700007
  article-title: Catalytic Enantioselective Ring-Opening Reactions of Cyclopropanes
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/acs.chemrev.0c00109
  contributor:
    fullname: Pirenne, V
– volume: 2012
  start-page: 2683
  year: 2012
  ident: WOS:000303440000002
  article-title: Transition-Metal-Mediated Cleavage and Activation of C-C Single Bonds
  publication-title: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1002/ejoc.201101616
  contributor:
    fullname: Ruhland, K
– start-page: 369
  year: 2006
  ident: WOS:000235146000001
  article-title: Catalytic enantioselective construction of all-carbon quaternary stereocenters
  publication-title: SYNTHESIS-STUTTGART
  doi: 10.1055/s-2006-926302
  contributor:
    fullname: Trost, BM
– volume: 33
  start-page: 610
  year: 2004
  ident: WOS:000225975600006
  article-title: Transition metal-catalyzed carbon-carbon bond activation
  publication-title: CHEMICAL SOCIETY REVIEWS
  doi: 10.1039/b308864m
  contributor:
    fullname: Jun, CH
– volume: 134
  start-page: 17502
  year: 2012
  ident: WOS:000310103800044
  article-title: Rhodium-Catalyzed Ring Opening of Benzocyclobutenols with Site-Selectivity Complementary to Thermal Ring Opening
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja309013a
  contributor:
    fullname: Ishida, N
– volume: 9
  start-page: 9127
  year: 2019
  ident: WOS:000489204000031
  article-title: Nickel-Catalyzed Enantioselective Reductive Aryl Fluoroalkenylation of Alkenes
  publication-title: ACS CATALYSIS
  doi: 10.1021/acscatal.9b03172
  contributor:
    fullname: Ma, T
– volume: 14
  start-page: 4365
  year: 2016
  ident: WOS:000376111000002
  article-title: Various difunctionalizations of acrylamide: an efficient approach to synthesize oxindoles
  publication-title: ORGANIC & BIOMOLECULAR CHEMISTRY
  doi: 10.1039/c6ob00554c
  contributor:
    fullname: Li, CC
– volume: 2003
  start-page: 2209
  year: 2003
  ident: WOS:000183839800003
  article-title: Construction of spiro[pyrrolidine-3,3′-oxindoles] -: Recent applications to the synthesis of oxindole alkaloids
  publication-title: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1002/ejoc.200300050
  contributor:
    fullname: Marti, C
– volume: 115
  start-page: 9410
  year: 2015
  ident: WOS:000361254500012
  article-title: Catalytic C-C Bond Activations via Oxidative Addition to Transition Metals
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/acs.chemrev.5b00138
  contributor:
    fullname: Souillart, L
– start-page: 3249
  year: 2009
  ident: WOS:000266555300031
  article-title: Oxindole synthesis by direct C-H, Ar-H coupling
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/b903516h
  contributor:
    fullname: Perry, A
– volume: 11
  start-page: 8942
  year: 2021
  ident: WOS:000674927200050
  article-title: Pd-Catalyzed Ring-Closing/Ring-Opening Cross Coupling Reactions: Enantioselective Diarylation of Unactivated Olefins
  publication-title: ACS CATALYSIS
  doi: 10.1021/acscatal.1c02277
  contributor:
    fullname: Liu, LT
– volume: 120
  start-page: 6500
  year: 1998
  ident: WOS:000074727600009
  article-title: Catalytic asymmetric synthesis of either enantiomer of the Calabar alkaloids physostigmine and physovenine
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  contributor:
    fullname: Matsuura, T
– start-page: 3003
  year: 2009
  ident: WOS:000270506800001
  article-title: Asymmetric Syntheses of Oxindole and Indole Spirocyclic Alkaloid Natural Products
  publication-title: SYNTHESIS-STUTTGART
  doi: 10.1055/s-0029-1216975
  contributor:
    fullname: Trost, BM
– start-page: 3389
  year: 2011
  ident: WOS:000296195400001
  article-title: Transition-Metal-Catalyzed Rearrangements of Small Cycloalkanes: Regioselectivity Trends in β-Carbon Elimination Reactions
  publication-title: SYNTHESIS-STUTTGART
  doi: 10.1055/s-0030-1260233
  contributor:
    fullname: Aïssa, C
– volume: 15
  start-page: 6166
  year: 2013
  ident: WOS:000329077700015
  article-title: Nickel-Catalyzed Aromatic C-H Alkylation with Secondary or Tertiary Alkyl-Bromine Bonds for the Construction of Indolones
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol403021p
  contributor:
    fullname: Liu, C
– volume: 82
  start-page: 9133
  year: 2017
  ident: WOS:000410004800035
  article-title: C-C Bond (Hetero)arylation of Ring-Fused Benzocyclobutenols and Application in the Assembly of Polycyclic Aromatic Hydrocarbons
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/acs.joc.7b01727
  contributor:
    fullname: Mao, WB
– volume: 21
  start-page: 185
  year: 2019
  ident: WOS:000455285800040
  article-title: Expeditious Synthesis of Isoquinolone Derivatives by Rhodium(I)-Catalyzed Annulation Reaction through C-C Bond Cleavage
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.8b03653
  contributor:
    fullname: He, YY
– volume: 58
  start-page: 6949
  year: 1993
  ident: WOS:A1993ML30700005
  article-title: CATALYTIC ASYMMETRIC-SYNTHESIS OF EITHER ENANTIOMER OF PHYSOSTIGMINE - FORMATION OF QUATERNARY CARBON CENTERS WITH HIGH ENANTIOSELECTION BY INTRAMOLECULAR HECK REACTIONS OF (Z)-2-BUTENANILIDES
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  contributor:
    fullname: ASHIMORI, A
– volume: 55
  start-page: 9714
  year: 2016
  ident: WOS:000383372700047
  article-title: Synthesis of Diversely Functionalized Oxindoles Enabled by Migratory Insertion of Isocyanide to a Transient σ-Alkylpalladium(II) Complex
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201603950
  contributor:
    fullname: Kong, WQ
– volume: 121
  start-page: 80
  year: 2021
  ident: D1OB02440J/cit17k/1
  publication-title: Chem. Rev.
  doi: 10.1021/acs.chemrev.0c00166
  contributor:
    fullname: Sokolova
– volume: 9
  start-page: 9127
  year: 2019
  ident: D1OB02440J/cit8c/1
  publication-title: ACS Catal.
  doi: 10.1021/acscatal.9b03172
  contributor:
    fullname: Ma
– volume: 47
  start-page: 4711
  year: 2008
  ident: D1OB02440J/cit12d/1
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.200800549
  contributor:
    fullname: Ruck
– start-page: 6821
  year: 2011
  ident: D1OB02440J/cit3a/1
  publication-title: Eur. J. Org. Chem.
  doi: 10.1002/ejoc.201100836
  contributor:
    fullname: Klein
– volume: 46
  start-page: 8484
  year: 2007
  ident: D1OB02440J/cit6a/1
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.200703408
  contributor:
    fullname: Kündig
– volume: 2
  start-page: 374
  year: 2021
  ident: D1OB02440J/cit15f/1
  publication-title: Green Synth. Catal.
  doi: 10.1016/j.gresc.2021.10.006
  contributor:
    fullname: Li
– volume: 1
  start-page: 567
  year: 2014
  ident: D1OB02440J/cit15a/1
  publication-title: Org. Chem. Front.
  doi: 10.1039/C4QO00053F
  contributor:
    fullname: Dermenci
– volume: 48
  start-page: 2615
  year: 2019
  ident: D1OB02440J/cit17i/1
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/C8CS00386F
  contributor:
    fullname: Sivaguru
– volume: 13
  start-page: 961
  year: 2007
  ident: D1OB02440J/cit12c/1
  publication-title: Chem. – Eur. J.
  doi: 10.1002/chem.200601016
  contributor:
    fullname: Pinto
– volume: 117
  start-page: 9404
  year: 2017
  ident: D1OB02440J/cit15e/1
  publication-title: Chem. Rev.
  doi: 10.1021/acs.chemrev.6b00599
  contributor:
    fullname: Fumagalli
– volume: 23
  start-page: 9520
  year: 2021
  ident: D1OB02440J/cit17p/1
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.1c03739
  contributor:
    fullname: Cao
– volume: 12
  start-page: 3446
  year: 2010
  ident: D1OB02440J/cit5c/1
  publication-title: Org. Lett.
  doi: 10.1021/ol1012668
  contributor:
    fullname: Klein
– volume: 138
  start-page: 13759
  year: 2016
  ident: D1OB02440J/cit15c/1
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.6b01656
  contributor:
    fullname: Murakami
– volume: 121
  start-page: 162
  year: 2021
  ident: D1OB02440J/cit17m/1
  publication-title: Chem. Rev.
  doi: 10.1021/acs.chemrev.0c00151
  contributor:
    fullname: Vicente
– volume: 121
  start-page: 264
  year: 2021
  ident: D1OB02440J/cit17o/1
  publication-title: Chem. Rev.
  doi: 10.1021/acs.chemrev.0c00569
  contributor:
    fullname: Murakami
– volume: 143
  start-page: 10282
  year: 2021
  ident: D1OB02440J/cit8f/1
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.1c03827
  contributor:
    fullname: Pan
– volume: 46
  start-page: 8748
  year: 2007
  ident: D1OB02440J/cit1d/1
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.200701342
  contributor:
    fullname: Galliford
– volume: 14
  start-page: 4365
  year: 2016
  ident: D1OB02440J/cit3c/1
  publication-title: Org. Biomol. Chem.
  doi: 10.1039/C6OB00554C
  contributor:
    fullname: Li
– volume: 131
  start-page: 8344
  year: 2009
  ident: D1OB02440J/cit6b/1
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja901018g
  contributor:
    fullname: Würtz
– volume: 121
  start-page: 3
  year: 2021
  ident: D1OB02440J/cit17j/1
  publication-title: Chem. Rev.
  doi: 10.1021/acs.chemrev.0c00346
  contributor:
    fullname: McDonald
– volume: 140
  start-page: 12364
  year: 2018
  ident: D1OB02440J/cit8b/1
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.8b08190
  contributor:
    fullname: Wang
– start-page: 3389
  year: 2011
  ident: D1OB02440J/cit17e/1
  publication-title: Synthesis
  doi: 10.1055/s-0030-1260233
  contributor:
    fullname: Aïssa
– volume: 21
  start-page: 7498
  year: 2019
  ident: D1OB02440J/cit8d/1
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.9b02788
  contributor:
    fullname: Xu
– volume: 52
  start-page: 12385
  year: 2013
  ident: D1OB02440J/cit12e/1
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201306532
  contributor:
    fullname: Piou
– volume: 22
  start-page: 18290
  year: 2016
  ident: D1OB02440J/cit17g/1
  publication-title: Chem. – Eur. J.
  doi: 10.1002/chem.201603382
  contributor:
    fullname: Chen
– start-page: 1273
  year: 2017
  ident: D1OB02440J/cit11b/1
  publication-title: Synthesis
  contributor:
    fullname: Chuang
– volume: 11
  start-page: 1566
  year: 2007
  ident: D1OB02440J/cit17b/1
  publication-title: Curr. Org. Chem.
  doi: 10.2174/138527207782418645
  contributor:
    fullname: Necas
– volume: 82
  start-page: 9133
  year: 2017
  ident: D1OB02440J/cit21b/1
  publication-title: J. Org. Chem.
  doi: 10.1021/acs.joc.7b01727
  contributor:
    fullname: Mao
– volume: 121
  start-page: 227
  year: 2021
  ident: D1OB02440J/cit17n/1
  publication-title: Chem. Rev.
  doi: 10.1021/acs.chemrev.0c00109
  contributor:
    fullname: Pirenne
– volume: 15
  start-page: 6166
  year: 2013
  ident: D1OB02440J/cit9/1
  publication-title: Org. Lett.
  doi: 10.1021/ol403021p
  contributor:
    fullname: Liu
– start-page: 1232
  year: 2016
  ident: D1OB02440J/cit17f/1
  publication-title: Eur. J. Org. Chem.
  doi: 10.1002/ejoc.201501291
  contributor:
    fullname: Kondo
– volume: 44
  start-page: 3249
  year: 2009
  ident: D1OB02440J/cit5b/1
  publication-title: Chem. Commun.
  doi: 10.1039/b903516h
  contributor:
    fullname: Perry
– volume: 20
  start-page: 921
  year: 2018
  ident: D1OB02440J/cit8a/1
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.7b03713
  contributor:
    fullname: Li
– volume: 329
  start-page: 1175
  year: 2010
  ident: D1OB02440J/cit2d/1
  publication-title: Science
  doi: 10.1126/science.1193225
  contributor:
    fullname: Rottmann
– volume: 8
  start-page: 2532
  year: 2021
  ident: D1OB02440J/cit7b/1
  publication-title: Org. Chem. Front.
  doi: 10.1039/D1QO00186H
  contributor:
    fullname: Chen
– volume: 33
  start-page: 610
  year: 2004
  ident: D1OB02440J/cit17a/1
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/B308864M
  contributor:
    fullname: Jun
– volume: 50
  start-page: 7740
  year: 2011
  ident: D1OB02440J/cit17d/1
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201101053
  contributor:
    fullname: Seiser
– start-page: 3003
  year: 2009
  ident: D1OB02440J/cit2c/1
  publication-title: Synthesis
  doi: 10.1055/s-0029-1216975
  contributor:
    fullname: Trost
– volume: 55
  start-page: 11921
  year: 2016
  ident: D1OB02440J/cit13/1
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201606955
  contributor:
    fullname: Desrosiers
– start-page: 731
  year: 2018
  ident: D1OB02440J/cit19e/1
  publication-title: Synlett
  contributor:
    fullname: Mao
– volume: 56
  start-page: 11927
  year: 2017
  ident: D1OB02440J/cit14/1
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201704922
  contributor:
    fullname: Jang
– volume: 48
  start-page: 437
  year: 1998
  ident: D1OB02440J/cit1a/1
  publication-title: Phytochemistry
  doi: 10.1016/S0031-9422(97)00946-1
  contributor:
    fullname: Anderton
– volume: 53
  start-page: 1605
  year: 2020
  ident: D1OB02440J/cit3b/1
  publication-title: Acc. Chem. Res.
  doi: 10.1021/acs.accounts.0c00297
  contributor:
    fullname: Marchese
– volume: 56
  start-page: 10920
  year: 2017
  ident: D1OB02440J/cit12g/1
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201706325
  contributor:
    fullname: Yoon
– volume: 76
  start-page: 9157
  year: 2011
  ident: D1OB02440J/cit21a/1
  publication-title: J. Org. Chem.
  doi: 10.1021/jo201632c
  contributor:
    fullname: Chtchemelinine
– volume: 902
  start-page: 120963
  year: 2019
  ident: D1OB02440J/cit12i/1
  publication-title: J. Organomet. Chem.
  doi: 10.1016/j.jorganchem.2019.120963
  contributor:
    fullname: Ramesh
– start-page: 541
  year: 1995
  ident: D1OB02440J/cit18b/1
  publication-title: Synlett
  doi: 10.1055/s-1995-5286
  contributor:
    fullname: Kraus
– volume: 55
  start-page: 9714
  year: 2016
  ident: D1OB02440J/cit2e/1
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201603950
  contributor:
    fullname: Kong
– volume: 47
  start-page: 1100
  year: 2011
  ident: D1OB02440J/cit16a/1
  publication-title: Chem. Commun.
  doi: 10.1039/C0CC02566F
  contributor:
    fullname: Murakami
– volume: 49
  start-page: 3432
  year: 2006
  ident: D1OB02440J/cit1c/1
  publication-title: J. Med. Chem.
  doi: 10.1021/jm051122a
  contributor:
    fullname: Ding
– volume: 50
  start-page: 15049
  year: 2014
  ident: D1OB02440J/cit11a/1
  publication-title: Chem. Commun.
  doi: 10.1039/C4CC07667B
  contributor:
    fullname: Li
– volume: 57
  start-page: 3233
  year: 2018
  ident: D1OB02440J/cit12h/1
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201800330
  contributor:
    fullname: Lu
– start-page: 2683
  year: 2012
  ident: D1OB02440J/cit16b/1
  publication-title: Eur. J. Org. Chem.
  doi: 10.1002/ejoc.201101616
  contributor:
    fullname: Ruhland
– volume: 121
  start-page: 140
  year: 2021
  ident: D1OB02440J/cit17l/1
  publication-title: Chem. Rev.
  doi: 10.1021/acs.chemrev.0c00167
  contributor:
    fullname: Cohen
– volume: 142
  start-page: 93
  year: 2020
  ident: D1OB02440J/cit6e/1
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.9b12698
  contributor:
    fullname: Kong
– volume: 51
  start-page: 1882
  year: 2015
  ident: D1OB02440J/cit19c/1
  publication-title: Chem. Commun.
  doi: 10.1039/C4CC09327E
  contributor:
    fullname: Ishida
– volume: 361
  start-page: 4961
  year: 2019
  ident: D1OB02440J/cit6f/1
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.201901100
  contributor:
    fullname: Lu
– volume: 58
  start-page: 6949
  year: 1993
  ident: D1OB02440J/cit12a/1
  publication-title: J. Org. Chem.
  doi: 10.1021/jo00077a005
  contributor:
    fullname: Ashimori
– volume: 7
  start-page: 2835
  year: 2009
  ident: D1OB02440J/cit17c/1
  publication-title: Org. Biomol. Chem.
  doi: 10.1039/b904405a
  contributor:
    fullname: Seiser
– volume: 120
  start-page: 6500
  year: 1998
  ident: D1OB02440J/cit12b/1
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja980788+
  contributor:
    fullname: Matsuura
– volume: 136
  start-page: 3013
  year: 2014
  ident: D1OB02440J/cit19b/1
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja500118w
  contributor:
    fullname: Xia
– volume: 130
  start-page: 14058
  year: 2008
  ident: D1OB02440J/cit4/1
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja807129e
  contributor:
    fullname: Wasa
– volume: 13
  start-page: 1666
  year: 2011
  ident: D1OB02440J/cit6c/1
  publication-title: Org. Lett.
  doi: 10.1021/ol200149s
  contributor:
    fullname: Liu
– volume: 18
  start-page: 328
  year: 2016
  ident: D1OB02440J/cit19d/1
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.5b03518
  contributor:
    fullname: Zhao
– volume: 55
  start-page: 1143
  year: 2016
  ident: D1OB02440J/cit20/1
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201509973
  contributor:
    fullname: Yu
– volume: 52
  start-page: 3972
  year: 2013
  ident: D1OB02440J/cit10/1
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201209475
  contributor:
    fullname: Li
– volume: 11
  start-page: 8942
  year: 2021
  ident: D1OB02440J/cit22/1
  publication-title: ACS Catal.
  doi: 10.1021/acscatal.1c02277
  contributor:
    fullname: Liu
– volume: 52
  start-page: 10817
  year: 2016
  ident: D1OB02440J/cit15d/1
  publication-title: Chem. Commun.
  doi: 10.1039/C6CC04359C
  contributor:
    fullname: Shaw
– volume: 134
  start-page: 17502
  year: 2012
  ident: D1OB02440J/cit19a/1
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja309013a
  contributor:
    fullname: Ishida
– volume: 54
  start-page: 414
  year: 2015
  ident: D1OB02440J/cit16c/1
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201405067
  contributor:
    fullname: Marek
– volume: 7
  start-page: 1340
  year: 2017
  ident: D1OB02440J/cit17h/1
  publication-title: ACS Catal.
  doi: 10.1021/acscatal.6b03210
  contributor:
    fullname: Chen
– volume: 22
  start-page: 3215
  year: 2020
  ident: D1OB02440J/cit7a/1
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.0c00999
  contributor:
    fullname: Liang
– volume: 2003
  start-page: 2219
  year: 2003
  ident: D1OB02440J/cit1b/1
  publication-title: Eur. J. Inorg. Chem.
  doi: 10.1002/ejic.200200535
  contributor:
    fullname: Faissner
– volume: 123
  start-page: 858
  year: 2016
  ident: D1OB02440J/cit1e/1
  publication-title: Eur. J. Med. Chem.
  doi: 10.1016/j.ejmech.2016.08.011
  contributor:
    fullname: Kaur
– volume: 137
  start-page: 16028
  year: 2015
  ident: D1OB02440J/cit6d/1
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.5b11625
  contributor:
    fullname: Kong
– volume: 60
  start-page: 14068
  year: 2021
  ident: D1OB02440J/cit8e/1
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.202102769
  contributor:
    fullname: Chen
– volume: 137
  start-page: 1341
  year: 2015
  ident: D1OB02440J/cit12f/1
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja512212x
  contributor:
    fullname: Wang
– volume: 115
  start-page: 9410
  year: 2015
  ident: D1OB02440J/cit15b/1
  publication-title: Chem. Rev.
  doi: 10.1021/acs.chemrev.5b00138
  contributor:
    fullname: Souillart
– volume: 136
  start-page: 169
  year: 2014
  ident: D1OB02440J/cit18a/1
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja407422q
  contributor:
    fullname: Ding
– volume: 37
  start-page: 369
  year: 2006
  ident: D1OB02440J/cit2b/1
  publication-title: ChemInform
  contributor:
    fullname: Trost
– volume: 21
  start-page: 185
  year: 2019
  ident: D1OB02440J/cit19f/1
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.8b03653
  contributor:
    fullname: He
– start-page: 2209
  year: 2003
  ident: D1OB02440J/cit2a/1
  publication-title: Eur. J. Org. Chem.
  doi: 10.1002/ejoc.200300050
  contributor:
    fullname: Marti
– volume: 48
  start-page: 1636
  year: 2009
  ident: D1OB02440J/cit5a/1
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.200805652
  contributor:
    fullname: Jia
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Snippet Catalytic construction of oxindoles bearing all-carbon-quaternary centers attracts wide attention from the synthetic chemistry community. Herein, we report a...
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SubjectTerms Alkenes
Carbon
Chemistry
Chemistry, Organic
Coupling
Covalent bonds
Enantiomers
Palladium
Physical Sciences
Science & Technology
Title A palladium-catalyzed sequential Heck coupling/C-C bond activation approach to oxindoles with all-carbon-quaternary centers
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https://www.ncbi.nlm.nih.gov/pubmed/35108719
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