Ortho- and Para-Selective Ruthenium-Catalyzed C(sp2)–H Oxygenations of Phenol Derivatives

Versatile ruthenium catalysts allowed for efficient direct oxygenations of aryl carbamates under remarkably mild reaction conditions. In addition to chelation-assisted C–H activation, the optimized ruthenium catalyst proved amenable to para-selective hydroxylations of anisoles without Lewis basic di...

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Published inOrganic letters Vol. 15; no. 13; pp. 3484 - 3486
Main Authors Liu, Weiping, Ackermann, Lutz
Format Journal Article
LanguageEnglish
Published WASHINGTON American Chemical Society 05.07.2013
Amer Chemical Soc
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Abstract Versatile ruthenium catalysts allowed for efficient direct oxygenations of aryl carbamates under remarkably mild reaction conditions. In addition to chelation-assisted C–H activation, the optimized ruthenium catalyst proved amenable to para-selective hydroxylations of anisoles without Lewis basic directing groups.
AbstractList Versatile ruthenium catalysts allowed for efficient direct oxygenations of aryl carbamates under remarkably mild reaction conditions. In addition to chelation-assisted C-H activation, the optimized ruthenium catalyst proved amenable to para-selective hydroxylations of anisoles without Lewis basic directing groups.Versatile ruthenium catalysts allowed for efficient direct oxygenations of aryl carbamates under remarkably mild reaction conditions. In addition to chelation-assisted C-H activation, the optimized ruthenium catalyst proved amenable to para-selective hydroxylations of anisoles without Lewis basic directing groups.
Versatile ruthenium catalysts allowed for efficient direct oxygenations of aryl carbamates under remarkably mild reaction conditions. In addition to chelation-assisted C-H activation, the optimized ruthenium catalyst proved amenable to para-selective hydroxylations of anisoles without Lewis basic directing groups.
Author Liu, Weiping
Ackermann, Lutz
AuthorAffiliation Georg-August-Universität
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Cites_doi 10.1021/ja2097095
10.1039/c1cs15085e
10.1002/anie.201203269
10.1016/1381-1169(95)00289-8
10.1007/128_2009_10
10.1021/cr900184e
10.1351/PAC-CON-09-08-17
10.1021/cr900005n
10.1002/anie.201207458
10.1021/ar3002798
10.1021/jo301964m
10.1039/c3cs60020c
10.1021/ol303520h
10.1039/c3ob27457h
10.1002/anie.201207479
10.1002/anie.200502767
10.1002/chem.201002273
10.1021/ar200185g
10.1021/ol301739f
10.1002/chem.201001363
10.1002/0470857277
10.1021/ol3018819
10.1002/chem.201000470
10.1039/c1cs15083a
10.1055/s-0032-1316853
10.1039/c1cs15013h
10.1021/ja031543m
10.1021/ol400437a
10.1021/ja907198n
10.1002/chem.200900281
10.1021/ja061715q
10.1038/nature11008
10.1021/ja206572w
10.1021/ja0541940
10.1021/ja401466y
10.1039/C2SC21524A
10.1039/c2cs15224j
10.1002/anie.201300957
10.1007/128_2009_9
10.1021/ol301104n
10.1002/anie.201201605
10.1038/nchem.1607
10.1021/ol302956s
10.1002/anie.201004703
10.1021/ja208286b
10.1039/b908581e
10.1021/cr300153j
10.1039/c2sc21524a
10.1021/cr300153J
10.1055/s-0032-1317575
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Keywords H BOND ACTIVATION
HYDROXYLATED ARENES
FUNCTIONALIZATION
CLEAVAGES
PALLADIUM
CONSTRUCTION
ALKOXYLATION
DIRECT ARYLATIONS
CONTAINING HETEROCYCLES
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References Dai H.-X. (ref3/cit3f) 2012; 134
Wencel-Delord J. (ref8/cit8) 2011; 40
Ciana C.-L. (ref10/cit10c) 2011; 50
Enthaler S. (ref2/cit2a) 2011; 40
Mo F. (ref3/cit3b) 2012; 51
Giri R. (ref3/cit3j) 2005; 44
Li B.-J. (ref6/cit6b) 2011; 17
Sun C.-L. (ref1/cit1j) 2010; 46
Dick A. R. (ref3/cit3i) 2005; 127
Arockiam P. B. (ref4/cit4c) 2012; 112
Hofmann N. (ref11/cit11a) 2013; 135
Shi Z. (ref1/cit1d) 2012; 41
Yang Y. (ref5/cit5e) 2012; 14
Chen X. (ref3/cit3h) 2006; 128
Yoneyama T. (ref3/cit3l) 1996; 108
Shan G. (ref5/cit5a) 2013; 11
Rappoport Z. (ref6/cit6c) 2003
Kamata K. (ref10/cit10b) 2012; 51
Zhang Y.-H. (ref3/cit3g) 2009; 131
Thirunavukkarasu V. S. (ref5/cit5c) 2012; 14
Shan G. (ref3/cit3c) 2012; 51
Daugulis O. (ref1/cit1g) 2010; 292
Colby D. A. (ref1/cit1h) 2010; 110
Thansandote P. (ref1/cit1k) 2009; 15
McMurray L. (ref1/cit1f) 2011; 40
Yan Y. (ref3/cit3a) 2013; 52
Jiang T.-S. (ref3/cit3d) 2012; 77
Kuhl N. (ref9/cit9) 2012; 51
Engle K. M. (ref1/cit1c) 2012
Yang F. (ref5/cit5b) 2013; 15
Wang X. (ref10/cit10a) 2011; 133
Ackermann L. (ref4/cit4d) 2010; 292
Yang X. (ref5/cit5f) 2013; 15
ref4/cit4b
Hickman A. J. (ref1/cit1e) 2012; 484
McMurtrey K. B. (ref3/cit3e) 2012; 14
Saidi O. (ref11/cit11b) 2011; 133
Ding Q. (ref6/cit6a) 2013; 45
Ackermann L. (ref7/cit7) 2010; 82
Kozhushkov S. I. (ref1/cit1b) 2013; 4
Satoh T. (ref1/cit1i) 2010; 16
Li B. (ref4/cit4a) 2013; 42
Wencel-Delord J. (ref1/cit1a) 2013; 5
Alonso D. A. (ref2/cit2b) 2010; 16
Lyons T. W. (ref2/cit2c) 2010; 110
Thirunavukkarasu V. S. (ref5/cit5d) 2012; 14
Dick A. R. (ref3/cit3k) 2004; 126
Wencel-Delord, J (WOS:000293858500016) 2011; 40
Chen, X (WOS:000237816300014) 2006; 128
Li, B (WOS:000320120000007) 2013; 42
Hofmann, N (WOS:000317872800053) 2013; 135
Ackermann, L (WOS:000280909300008) 2010; 292
Ding, QP (WOS:000313322900002) 2013; 45
Dick, AR (WOS:000189279700021) 2004; 126
Kozhushkov, SI (WOS:000314474900001) 2013; 4
Arockiam, PB (WOS:000311239600009) 2012; 112
Lyons, TW (WOS:000274705900016) 2010; 110
Colby, DA (WOS:000274705900003) 2010; 110
Hickman, AJ (WOS:000303149900024) 2012; 484
Ackermann, L (WOS:000331775200001) 2014; 47
Dai, HX (WOS:000301084200035) 2012; 134
Engle, K. M. (000321605800074.14) 2012
Giri, R (WOS:000233515700017) 2005; 44
Kamata, K (WOS:000306314300042) 2012; 51
Yoneyama, T (WOS:A1996UH25000007) 1996; 108
Ackermann, L (WOS:000279657900005) 2010; 82
Wencel-Delord, J (WOS:000317961700009) 2013; 5
Rappoport, Z. (000321605800074.29) 2003
Yang, XL (WOS:000319720900003) 2013; 15
Yang, FZ (WOS:000314559000075) 2013; 15
Enthaler, S (WOS:000295037400004) 2011; 40
Satoh, T (WOS:000283386600001) 2010; 16
Alonso, DA (WOS:000277988900004) 2010; 16
Jiang, TS (WOS:000311190200007) 2012; 77
Yang, YQ (WOS:000304682700056) 2012; 14
Li, BJ (WOS:000287787100001) 2011; 17
Ciana, CL (WOS:000286729300020) 2011; 50
Shan, G (WOS:000316011300014) 2013; 11
Thirunavukkarasu, VS (WOS:000307526900045) 2012; 14
Thansandote, P (WOS:000267278900001) 2009; 15
McMurtrey, KB (WOS:000307526900016) 2012; 14
Mo, FY (WOS:000312552900032) 2012; 51
Shan, G (WOS:000312552900031) 2012; 51
Shi, ZZ (WOS:000301985300020) 2012; 41
Daugulis, O (WOS:000280909300003) 2010; 292
Wang, XS (WOS:000295241400026) 2011; 133
Kuhl, N (WOS:000309406900006) 2012; 51
Dick, AR (WOS:000231928800021) 2005; 127
Saidi, O (WOS:000297606500011) 2011; 133
Sun, CL (WOS:000274207000002) 2010; 46
McMurray, L (WOS:000288609400005) 2011; 40
Zhang, YH (WOS:000271271800028) 2009; 131
Yan, YP (WOS:000319741100028) 2013; 52
Thirunavukkarasu, VS (WOS:000312564500023) 2012; 14
References_xml – volume: 134
  start-page: 134
  year: 2012
  ident: ref3/cit3f
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja2097095
– volume: 40
  start-page: 4912
  year: 2011
  ident: ref2/cit2a
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/c1cs15085e
– volume: 51
  start-page: 10236
  year: 2012
  ident: ref9/cit9
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201203269
– volume: 108
  start-page: 35
  year: 1996
  ident: ref3/cit3l
  publication-title: J. Mol. Catal. A
  doi: 10.1016/1381-1169(95)00289-8
– volume: 292
  start-page: 57
  year: 2010
  ident: ref1/cit1g
  publication-title: Top. Curr. Chem.
  doi: 10.1007/128_2009_10
– volume: 110
  start-page: 1147
  year: 2010
  ident: ref2/cit2c
  publication-title: Chem. Rev.
  doi: 10.1021/cr900184e
– volume: 82
  start-page: 1403
  year: 2010
  ident: ref7/cit7
  publication-title: Pure Appl. Chem.
  doi: 10.1351/PAC-CON-09-08-17
– volume: 110
  start-page: 624
  year: 2010
  ident: ref1/cit1h
  publication-title: Chem. Rev.
  doi: 10.1021/cr900005n
– volume: 51
  start-page: 13070
  year: 2012
  ident: ref3/cit3c
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201207458
– ident: ref4/cit4b
  doi: 10.1021/ar3002798
– volume: 77
  start-page: 9504
  year: 2012
  ident: ref3/cit3d
  publication-title: J. Org. Chem.
  doi: 10.1021/jo301964m
– volume: 42
  start-page: 5744
  year: 2013
  ident: ref4/cit4a
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/c3cs60020c
– volume: 15
  start-page: 718
  year: 2013
  ident: ref5/cit5b
  publication-title: Org. Lett.
  doi: 10.1021/ol303520h
– volume: 11
  start-page: 2318
  year: 2013
  ident: ref5/cit5a
  publication-title: Org. Biomol. Chem.
  doi: 10.1039/c3ob27457h
– volume: 51
  start-page: 13075
  year: 2012
  ident: ref3/cit3b
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201207479
– volume: 44
  start-page: 7420
  year: 2005
  ident: ref3/cit3j
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.200502767
– volume: 17
  start-page: 1728
  year: 2011
  ident: ref6/cit6b
  publication-title: Chem.—Eur. J.
  doi: 10.1002/chem.201002273
– start-page: 788
  year: 2012
  ident: ref1/cit1c
  publication-title: Acc. Chem. Res.
  doi: 10.1021/ar200185g
– volume: 14
  start-page: 4094
  year: 2012
  ident: ref3/cit3e
  publication-title: Org. Lett.
  doi: 10.1021/ol301739f
– volume: 16
  start-page: 11212
  year: 2010
  ident: ref1/cit1i
  publication-title: Chem.—Eur. J.
  doi: 10.1002/chem.201001363
– volume-title: The Chemistry of Phenols
  year: 2003
  ident: ref6/cit6c
  doi: 10.1002/0470857277
– volume: 14
  start-page: 4210
  year: 2012
  ident: ref5/cit5d
  publication-title: Org. Lett.
  doi: 10.1021/ol3018819
– volume: 16
  start-page: 5274
  year: 2010
  ident: ref2/cit2b
  publication-title: Chem.—Eur. J.
  doi: 10.1002/chem.201000470
– volume: 40
  start-page: 4740
  year: 2011
  ident: ref8/cit8
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/c1cs15083a
– volume: 45
  start-page: 1
  year: 2013
  ident: ref6/cit6a
  publication-title: Synthesis
  doi: 10.1055/s-0032-1316853
– volume: 40
  start-page: 1885
  year: 2011
  ident: ref1/cit1f
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/c1cs15013h
– volume: 126
  start-page: 2300
  year: 2004
  ident: ref3/cit3k
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja031543m
– volume: 15
  start-page: 2334
  year: 2013
  ident: ref5/cit5f
  publication-title: Org. Lett.
  doi: 10.1021/ol400437a
– volume: 131
  start-page: 14654
  year: 2009
  ident: ref3/cit3g
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja907198n
– volume: 15
  start-page: 5874
  year: 2009
  ident: ref1/cit1k
  publication-title: Chem.—Eur. J.
  doi: 10.1002/chem.200900281
– volume: 128
  start-page: 6790
  year: 2006
  ident: ref3/cit3h
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja061715q
– volume: 484
  start-page: 177
  year: 2012
  ident: ref1/cit1e
  publication-title: Nature
  doi: 10.1038/nature11008
– volume: 133
  start-page: 13864
  year: 2011
  ident: ref10/cit10a
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja206572w
– volume: 127
  start-page: 12790
  year: 2005
  ident: ref3/cit3i
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja0541940
– volume: 135
  start-page: 5877
  year: 2013
  ident: ref11/cit11a
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja401466y
– volume: 4
  start-page: 886
  year: 2013
  ident: ref1/cit1b
  publication-title: Chem. Sci.
  doi: 10.1039/C2SC21524A
– volume: 41
  start-page: 3381
  year: 2012
  ident: ref1/cit1d
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/c2cs15224j
– volume: 52
  start-page: 5827
  year: 2013
  ident: ref3/cit3a
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201300957
– volume: 292
  start-page: 211
  year: 2010
  ident: ref4/cit4d
  publication-title: Top. Curr. Chem.
  doi: 10.1007/128_2009_9
– volume: 14
  start-page: 2874
  year: 2012
  ident: ref5/cit5e
  publication-title: Org. Lett.
  doi: 10.1021/ol301104n
– volume: 51
  start-page: 7275
  year: 2012
  ident: ref10/cit10b
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201201605
– volume: 5
  start-page: 369
  year: 2013
  ident: ref1/cit1a
  publication-title: Nat. Chem.
  doi: 10.1038/nchem.1607
– volume: 14
  start-page: 6206
  year: 2012
  ident: ref5/cit5c
  publication-title: Org. Lett.
  doi: 10.1021/ol302956s
– volume: 50
  start-page: 458
  year: 2011
  ident: ref10/cit10c
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201004703
– volume: 133
  start-page: 19298
  year: 2011
  ident: ref11/cit11b
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja208286b
– volume: 46
  start-page: 677
  year: 2010
  ident: ref1/cit1j
  publication-title: Chem. Commun.
  doi: 10.1039/b908581e
– volume: 112
  start-page: 5879
  year: 2012
  ident: ref4/cit4c
  publication-title: Chem. Rev.
  doi: 10.1021/cr300153j
– volume: 44
  start-page: 7420
  year: 2005
  ident: WOS:000233515700017
  article-title: Pd-catalyzed stereoselective oxidation of methyl groups by inexpensive oxidants under mild conditions: A dual role for carboxylic anhydrides in catalytic C-H bond oxidation
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.200502767
– volume: 11
  start-page: 2318
  year: 2013
  ident: WOS:000316011300014
  article-title: Broadening the catalyst and reaction scope of regio- and chemoselective C-H oxygenation: a convenient and scalable approach to 2-acylphenols by intriguing Rh(II) and Ru(II) catalysis
  publication-title: ORGANIC & BIOMOLECULAR CHEMISTRY
  doi: 10.1039/c3ob27457h
– volume: 40
  start-page: 4740
  year: 2011
  ident: WOS:000293858500016
  article-title: Towards mild metal-catalyzed C-H bond activation
  publication-title: CHEMICAL SOCIETY REVIEWS
  doi: 10.1039/c1cs15083a
– volume: 292
  start-page: 57
  year: 2010
  ident: WOS:000280909300003
  article-title: Palladium and Copper Catalysis in Regioselective, Intermolecular Coupling of C-H and C-Hal Bonds
  publication-title: C-H ACTIVATION
  doi: 10.1007/128_2009_10
– volume: 110
  start-page: 1147
  year: 2010
  ident: WOS:000274705900016
  article-title: Palladium-Catalyzed Ligand-Directed C-H Functionalization Reactions
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/cr900184e
– start-page: 788
  year: 2012
  ident: 000321605800074.14
  publication-title: Acc. Chem. Res.
– volume: 14
  start-page: 2874
  year: 2012
  ident: WOS:000304682700056
  article-title: Ruthenium(II)-Catalyzed Synthesis of Hydroxylated Arenes with Ester as an Effective Directing Group
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol301104n
– volume: 484
  start-page: 177
  year: 2012
  ident: WOS:000303149900024
  article-title: High-valent organometallic copper and palladium in catalysis
  publication-title: NATURE
  doi: 10.1038/nature11008
– volume: 47
  start-page: 281
  year: 2014
  ident: WOS:000331775200001
  article-title: Carboxylate-Assisted Ruthenium-Catalyzed Alkyne Annulations by C-H/Het-H Bond Functionalizations
  publication-title: ACCOUNTS OF CHEMICAL RESEARCH
  doi: 10.1021/ar3002798
– volume: 17
  start-page: 1728
  year: 2011
  ident: WOS:000287787100001
  article-title: Activation of "Inert" Alkenyl/Aryl C-O Bond and Its Application in Cross-Coupling Reactions
  publication-title: CHEMISTRY-A EUROPEAN JOURNAL
  doi: 10.1002/chem.201002273
– volume: 14
  start-page: 4094
  year: 2012
  ident: WOS:000307526900016
  article-title: Pd-Catalyzed C-H Fluorination with Nucleophilic Fluoride
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol301739f
– volume: 108
  start-page: 35
  year: 1996
  ident: WOS:A1996UH25000007
  article-title: Pd(II) catalyzed acetoxylation of arenes with iodosyl acetate
  publication-title: JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL
– volume: 128
  start-page: 6790
  year: 2006
  ident: WOS:000237816300014
  article-title: Cu(II)-catalyzed functionalizations of aryl C-H bonds using O-2 as an oxidant
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja061715q
– volume: 15
  start-page: 2334
  year: 2013
  ident: WOS:000319720900003
  article-title: Synthesis of 2-Aminophenols and Heterocycles by Ru-Catalyzed C-H Mono- and Dihydroxylation
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol400437a
– volume: 16
  start-page: 11212
  year: 2010
  ident: WOS:000283386600001
  article-title: Oxidative Coupling of Aromatic Substrates with Alkynes and Alkenes under Rhodium Catalysis
  publication-title: CHEMISTRY-A EUROPEAN JOURNAL
  doi: 10.1002/chem.201001363
– volume: 82
  start-page: 1403
  year: 2010
  ident: WOS:000279657900005
  article-title: Transition-metal-catalyzed direct arylations via C-H bond cleavages
  publication-title: PURE AND APPLIED CHEMISTRY
  doi: 10.1351/PAC-CON-09-08-17
– volume: 127
  start-page: 12790
  year: 2005
  ident: WOS:000231928800021
  article-title: Unusually stable palladium(IV) complexes: Detailed mechanistic investigation of C-O bond-forming reductive elimination
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja0541940
– volume: 16
  start-page: 5274
  year: 2010
  ident: WOS:000277988900004
  article-title: Transition-Metal-Catalyzed Synthesis of Hydroxylated Arenes
  publication-title: CHEMISTRY-A EUROPEAN JOURNAL
  doi: 10.1002/chem.201000470
– volume: 15
  start-page: 718
  year: 2013
  ident: WOS:000314559000075
  article-title: Ruthenium-Catalyzed C-H Oxygenation on Aryl Weinreb Amides
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol303520h
– volume: 4
  start-page: 886
  year: 2013
  ident: WOS:000314474900001
  article-title: Ruthenium-catalyzed direct oxidative alkenylation of arenes through twofold C-H bond functionalization
  publication-title: CHEMICAL SCIENCE
  doi: 10.1039/c2sc21524a
– volume: 135
  start-page: 5877
  year: 2013
  ident: WOS:000317872800053
  article-title: meta-Selective C-H Bond Alkylation with Secondary Alkyl Halides
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja401466y
– volume: 52
  start-page: 5827
  year: 2013
  ident: WOS:000319741100028
  article-title: PdCl2 and N-Hydroxyphthalimide Co-catalyzed C-sp2-H Hydroxylation by Dioxygen Activation
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201300957
– volume: 51
  start-page: 7275
  year: 2012
  ident: WOS:000306314300042
  article-title: Chemo- and Regioselective Direct Hydroxylation of Arenes with Hydrogen Peroxide Catalyzed by a Divanadium-Substituted Phosphotungstate
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201201605
– volume: 133
  start-page: 19298
  year: 2011
  ident: WOS:000297606500011
  article-title: Ruthenium-Catalyzed Meta Sulfonation of 2-Phenylpyridines
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja208286b
– volume: 134
  start-page: 134
  year: 2012
  ident: WOS:000301084200035
  article-title: Pd-Catalyzed Oxidative ortho-C-H Borylation of Arenes
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja2097095
– volume: 292
  start-page: 211
  year: 2010
  ident: WOS:000280909300008
  article-title: Ruthenium-Catalyzed Direct Arylations Through C-H Bond Cleavages
  publication-title: C-H ACTIVATION
  doi: 10.1007/128_2009_9
– volume: 14
  start-page: 6206
  year: 2012
  ident: WOS:000312564500023
  article-title: Ruthenium-Catalyzed C-H Bond Oxygenations with Weakly Coordinating Ketones
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol302956s
– volume: 110
  start-page: 624
  year: 2010
  ident: WOS:000274705900003
  article-title: Rhodium-Catalyzed C-C Bond Formation via Heteroatom-Directed C-H Bond Activation
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/cr900005n
– volume: 40
  start-page: 1885
  year: 2011
  ident: WOS:000288609400005
  article-title: Recent developments in natural product synthesis using metal-catalysed C-H bond functionalisation
  publication-title: CHEMICAL SOCIETY REVIEWS
  doi: 10.1039/c1cs15013h
– volume: 14
  start-page: 4210
  year: 2012
  ident: WOS:000307526900045
  article-title: Ruthenium-Catalyzed Oxidative C(sp(2))-H Bond Hydroxylation: Site-Selective C-O Bond Formation on Benzamides
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol3018819
– volume: 126
  start-page: 2300
  year: 2004
  ident: WOS:000189279700021
  article-title: A highly selective catalytic method for the oxidative functionalization of C-H bonds
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja031543m
– volume: 112
  start-page: 5879
  year: 2012
  ident: WOS:000311239600009
  article-title: Ruthenium(II)-Catalyzed C-H Bond Activation and Functionalization
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/cr300153J
– volume: 40
  start-page: 4912
  year: 2011
  ident: WOS:000295037400004
  article-title: Palladium-catalysed hydroxylation and alkoxylation
  publication-title: CHEMICAL SOCIETY REVIEWS
  doi: 10.1039/c1cs15085e
– volume: 133
  start-page: 13864
  year: 2011
  ident: WOS:000295241400026
  article-title: Pd(II)-Catalyzed para-Selective C-H Arylation of Monosubstituted Arenes
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja206572w
– volume: 42
  start-page: 5744
  year: 2013
  ident: WOS:000320120000007
  article-title: sp(2) C-H bond activation in water and catalytic crosscoupling reactions
  publication-title: CHEMICAL SOCIETY REVIEWS
  doi: 10.1039/c3cs60020c
– volume: 77
  start-page: 9504
  year: 2012
  ident: WOS:000311190200007
  article-title: Palladium-Catalyzed Ortho-Alkoxylation of Anilides via C-H Activation
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/jo301964m
– volume: 46
  start-page: 677
  year: 2010
  ident: WOS:000274207000002
  article-title: Pd-catalyzed oxidative coupling with organometallic reagents via C-H activation
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/b908581e
– volume: 51
  start-page: 10236
  year: 2012
  ident: WOS:000309406900006
  article-title: Beyond Directing Groups: Transition-Metal-Catalyzed C-H Activation of Simple Arenes
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201203269
– volume: 45
  start-page: 1
  year: 2013
  ident: WOS:000313322900002
  article-title: Recent Advances in Phenol Dearomatization and Its Application in Complex Syntheses
  publication-title: SYNTHESIS-STUTTGART
  doi: 10.1055/s-0032-1317575
– volume: 15
  start-page: 5874
  year: 2009
  ident: WOS:000267278900001
  article-title: Construction of Nitrogen-Containing Heterocycles by C-H Bond Functionalization
  publication-title: CHEMISTRY-A EUROPEAN JOURNAL
  doi: 10.1002/chem.200900281
– volume: 51
  start-page: 13075
  year: 2012
  ident: WOS:000312552900032
  article-title: Synthesis of ortho-Acylphenols through the Palladium-Catalyzed Ketone-Directed Hydroxylation of Arenes
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201207479
– volume: 51
  start-page: 13070
  year: 2012
  ident: WOS:000312552900031
  article-title: Pd-Catalyzed C-H Oxygenation with TFA/TFAA: Expedient Access to Oxygen-Containing Heterocycles and Late-Stage Drug Modification
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201207458
– volume: 5
  start-page: 369
  year: 2013
  ident: WOS:000317961700009
  article-title: C-H bond activation enables the rapid construction and late-stage diversification of functional molecules
  publication-title: NATURE CHEMISTRY
  doi: 10.1038/nchem.1607
– volume: 131
  start-page: 14654
  year: 2009
  ident: WOS:000271271800028
  article-title: Pd(II)-Catalyzed Hydroxylation of Arenes with 1 atm of O-2 or Air
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja907198n
– year: 2003
  ident: 000321605800074.29
  publication-title: The Chemistry of Phenols
– volume: 50
  start-page: 458
  year: 2011
  ident: WOS:000286729300020
  article-title: A Highly Para-Selective Copper(II)-Catalyzed Direct Arylation of Aniline and Phenol Derivatives
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201004703
– volume: 41
  start-page: 3381
  year: 2012
  ident: WOS:000301985300020
  article-title: Recent advances in transition-metal catalyzed reactions using molecular oxygen as the oxidant
  publication-title: CHEMICAL SOCIETY REVIEWS
  doi: 10.1039/c2cs15224j
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Snippet Versatile ruthenium catalysts allowed for efficient direct oxygenations of aryl carbamates under remarkably mild reaction conditions. In addition to...
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SubjectTerms carbamates
carbon-hydrogen bond activation
catalysts
chemical reactions
chemical structure
Chemistry
Chemistry, Organic
phenol
Physical Sciences
ruthenium
Science & Technology
Title Ortho- and Para-Selective Ruthenium-Catalyzed C(sp2)–H Oxygenations of Phenol Derivatives
URI http://dx.doi.org/10.1021/ol401535k
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https://www.ncbi.nlm.nih.gov/pubmed/23799802
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Volume 15
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