Nickel(0)‐Catalyzed Hydroarylation of Styrenes and 1,3‐Dienes with Organoboron Compounds

A Ni‐catalyzed hydroarylation of styrenes and 1,3‐dienes with organoboron compounds has been developed. The reaction offers a highly selective approach to diarylalkanes and allylarenes under redox‐neutral conditions. In this hydroarylation reaction, a new strategy that uses the proton of methanol to...

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Published inAngewandte Chemie International Edition Vol. 57; no. 2; pp. 461 - 464
Main Authors Xiao, Li‐Jun, Cheng, Lei, Feng, Wei‐Min, Li, Mao‐Lin, Xie, Jian‐Hua, Zhou, Qi‐Lin
Format Journal Article
LanguageEnglish
Published WEINHEIM Wiley 08.01.2018
Wiley Subscription Services, Inc
EditionInternational ed. in English
Subjects
alkenes
Chemistry
Chemistry, Multidisciplinary
coupling reactions
Dienes
hydroarylation
Nickel
Nickel compounds
Organoboron compounds
organoboron reagents
Physical Sciences
Retinoic acid
Science & Technology
Styrenes
nickel
RAW-MATERIALS
coupling reactions
HYDROXYLATION
alkenes
MONOOXYGENASES
FATTY-ACID
CHEMISTRY
HYDROGEN-PEROXIDE
P450
hydroarylation
organoboron reagents
H2O2-DEPENDENT CYTOCHROME P450(SP-ALPHA)
LACTATE OXIDASE
OXYFUNCTIONALIZATION REACTIONS
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Abstract A Ni‐catalyzed hydroarylation of styrenes and 1,3‐dienes with organoboron compounds has been developed. The reaction offers a highly selective approach to diarylalkanes and allylarenes under redox‐neutral conditions. In this hydroarylation reaction, a new strategy that uses the proton of methanol to generate the active catalyst species Ni−H was developed. The Ni‐catalyzed hydroarylation, combined with a Ir‐catalyzed C−H borylation, affords a very efficient and straightforward access to a retinoic acid receptor agonist. OH yeah: A nickel(0)‐catalyzed hydroarylation of alkenes with organoboron reagents using an alcohol OH group as the H‐atom source is reported. The reaction offers a highly selective approach to diarylalkanes and allylarenes under redox‐neutral conditions.
AbstractList A Ni-catalyzed hydroarylation of styrenes and 1,3-dienes with organoboron compounds has been developed. The reaction offers a highly selective approach to diarylalkanes and allylarenes under redox-neutral conditions. In this hydroarylation reaction, a new strategy that uses the proton of methanol to generate the active catalyst species Ni-H was developed. The Ni-catalyzed hydroarylation, combined with a Ir-catalyzed C-H borylation, affords a very efficient and straightforward access to a retinoic acid receptor agonist.
A Ni‐catalyzed hydroarylation of styrenes and 1,3‐dienes with organoboron compounds has been developed. The reaction offers a highly selective approach to diarylalkanes and allylarenes under redox‐neutral conditions. In this hydroarylation reaction, a new strategy that uses the proton of methanol to generate the active catalyst species Ni−H was developed. The Ni‐catalyzed hydroarylation, combined with a Ir‐catalyzed C−H borylation, affords a very efficient and straightforward access to a retinoic acid receptor agonist.
A Ni‐catalyzed hydroarylation of styrenes and 1,3‐dienes with organoboron compounds has been developed. The reaction offers a highly selective approach to diarylalkanes and allylarenes under redox‐neutral conditions. In this hydroarylation reaction, a new strategy that uses the proton of methanol to generate the active catalyst species Ni−H was developed. The Ni‐catalyzed hydroarylation, combined with a Ir‐catalyzed C−H borylation, affords a very efficient and straightforward access to a retinoic acid receptor agonist. OH yeah: A nickel(0)‐catalyzed hydroarylation of alkenes with organoboron reagents using an alcohol OH group as the H‐atom source is reported. The reaction offers a highly selective approach to diarylalkanes and allylarenes under redox‐neutral conditions.
A Ni-catalyzed hydroarylation of styrenes and 1,3-dienes with organoboron compounds has been developed. The reaction offers a highly selective approach to diarylalkanes and allylarenes under redox-neutral conditions. In this hydroarylation reaction, a new strategy that uses the proton of methanol to generate the active catalyst species Ni-H was developed. The Ni-catalyzed hydroarylation, combined with a Ir-catalyzed C-H borylation, affords a very efficient and straightforward access to a retinoic acid receptor agonist.A Ni-catalyzed hydroarylation of styrenes and 1,3-dienes with organoboron compounds has been developed. The reaction offers a highly selective approach to diarylalkanes and allylarenes under redox-neutral conditions. In this hydroarylation reaction, a new strategy that uses the proton of methanol to generate the active catalyst species Ni-H was developed. The Ni-catalyzed hydroarylation, combined with a Ir-catalyzed C-H borylation, affords a very efficient and straightforward access to a retinoic acid receptor agonist.
Author Li, Mao‐Lin
Zhou, Qi‐Lin
Cheng, Lei
Xie, Jian‐Hua
Xiao, Li‐Jun
Feng, Wei‐Min
Author_xml – sequence: 1
  givenname: Li‐Jun
  surname: Xiao
  fullname: Xiao, Li‐Jun
  organization: Nankai University
– sequence: 2
  givenname: Lei
  surname: Cheng
  fullname: Cheng, Lei
  organization: Nankai University
– sequence: 3
  givenname: Wei‐Min
  surname: Feng
  fullname: Feng, Wei‐Min
  organization: Nankai University
– sequence: 4
  givenname: Mao‐Lin
  surname: Li
  fullname: Li, Mao‐Lin
  organization: Nankai University
– sequence: 5
  givenname: Jian‐Hua
  surname: Xie
  fullname: Xie, Jian‐Hua
  organization: Collaborative Innovation Center of Chemical Science and Engineering (Tianjin)
– sequence: 6
  givenname: Qi‐Lin
  orcidid: 0000-0002-4700-3765
  surname: Zhou
  fullname: Zhou, Qi‐Lin
  email: qlzhou@nankai.edu.cn
  organization: Collaborative Innovation Center of Chemical Science and Engineering (Tianjin)
BackLink https://www.ncbi.nlm.nih.gov/pubmed/29159912$$D View this record in MEDLINE/PubMed
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Cites_doi 10.1021/acs.chemrev.6b00574
10.1002/anie.200705317
10.1021/om300819d
10.1002/ange.201703400
10.1021/ja805296k
10.1039/C6GC00549G
10.1021/jacs.6b04566
10.1021/ja4034999
10.1021/ja0693183
10.1002/ange.201511975
10.1246/cl.150913
10.1002/cmdc.201500069
10.1021/ar200206a
10.1021/jacs.7b04973
10.1002/ange.200705317
10.1021/ja057654y
10.1021/ar960318p
10.1002/anie.201703400
10.1021/jacs.6b08507
10.1021/jm901446n
10.1021/jacs.6b11962
10.1021/jacs.7b08064
10.1021/jacs.7b07637
10.1021/om900045p
10.1021/ja076746f
10.1021/ja104505t
10.1038/ncomms11129
10.1002/cmdc.201000456
10.1002/(SICI)1521-3765(19981204)4:12<2405::AID-CHEM2405>3.0.CO;2-0
10.1021/jm9502293
10.1021/ja105010t
10.1021/cr500610p
10.1002/anie.201511975
10.1021/jacs.6b00024
10.1002/cctc.201600536
10.1016/j.tibtech.2011.06.012
10.1002/anie.201105308
10.1002/anie.201002767
10.1021/acscatal.6b03453
10.1021/jacs.6b01716
10.1016/j.copbio.2016.07.004
10.1016/j.tibtech.2012.12.007
10.1074/jbc.M111.245225
10.1039/b915078a
10.1016/j.bbrc.2007.07.155
10.1021/cs300001x
10.1016/j.tibs.2012.11.006
10.1002/anie.201502925
10.1016/S1388-2481(04)00084-0
10.1021/cr9002193
10.1007/s00775-014-1106-9
10.1002/anie.201507881
10.1021/acs.chemrev.7b00033
10.1111/j.1742-4658.2010.07949.x
10.1021/cr0307143
10.1016/j.jbiotec.2006.01.026
10.1093/nar/gkt1060
10.1002/bab.1063
10.1016/j.bmc.2014.05.074
10.1128/AEM.02580-10
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Issue 2
Keywords nickel
RAW-MATERIALS
coupling reactions
HYDROXYLATION
alkenes
MONOOXYGENASES
FATTY-ACID
CHEMISTRY
HYDROGEN-PEROXIDE
P450
hydroarylation
organoboron reagents
H2O2-DEPENDENT CYTOCHROME P450(SP-ALPHA)
LACTATE OXIDASE
OXYFUNCTIONALIZATION REACTIONS
Language English
License http://onlinelibrary.wiley.com/termsAndConditions#vor
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References 2010; 53
2007; 129
1996; 39
2011
2002; 35
2015; 10
2008 2008; 47 120
2017 2017; 56 129
2016; 18
2011; 6
2012; 31
2017; 117
2017; 139
2009; 28
2016; 7
2016 2016; 55 128
2015; 115
2010; 132
2013; 135
2016; 138
2012; 45
2006; 128
1998; 4
2008; 130
2016; 45
van Leeuwen P. W. N. (e_1_2_2_1_1) 2011
e_1_2_2_3_2
e_1_2_2_24_2
e_1_2_2_4_2
e_1_2_2_23_2
e_1_2_2_5_2
e_1_2_2_6_1
e_1_2_2_21_2
e_1_2_2_22_1
e_1_2_2_20_2
e_1_2_2_2_1
e_1_2_2_7_2
e_1_2_2_8_2
e_1_2_2_28_2
e_1_2_2_29_1
e_1_2_2_27_2
e_1_2_2_26_2
e_1_2_2_9_2
e_1_2_2_25_2
e_1_2_2_13_2
e_1_2_2_36_2
e_1_2_2_37_1
e_1_2_2_12_2
e_1_2_2_38_1
e_1_2_2_10_2
e_1_2_2_11_1
e_1_2_2_30_1
e_1_2_2_19_2
e_1_2_2_17_3
e_1_2_2_18_2
e_1_2_2_31_2
e_1_2_2_17_2
e_1_2_2_32_2
e_1_2_2_33_1
e_1_2_2_15_3
e_1_2_2_16_2
e_1_2_2_34_1
e_1_2_2_15_2
e_1_2_2_13_3
e_1_2_2_14_2
e_1_2_2_35_2
Matsunaga, I (WOS:000082583500009) 1999; 34
Ni, Y (WOS:000368069200064) 2016; 55
Perez, DI (WOS:000271506700047) 2009
de Montellano, PRO (WOS:000274705900011) 2010; 110
Schrittwieser, JH (WOS:000419999700007) 2018; 118
Lütz, S (WOS:000221735200013) 2004; 6
Matsunaga, I (WOS:A1996UM44200035) 1996; 386
Rude, MA (WOS:000287700100023) 2011; 77
KOUBEK, E (WOS:A19633102B00025) 1963; 85
Dennig, A (WOS:000358051600046) 2015; 54
Bernhardt, R (WOS:000238620900011) 2006; 124
Denisov, I. G. (000419110500013.7) 2015
Ramanan, R (WOS:000377151400017) 2016; 138
Hill, K (WOS:000165247200007) 2000; 72
Munro, AW (WOS:000316243400004) 2013; 38
Fasan, R (WOS:000302387600022) 2012; 2
Paul, CE (WOS:000343271900020) 2014; 22
Biermann, U (WOS:000289514100007) 2011; 50
(000419110500013.10) 2015; 127
Sheng, BB (WOS:000386916400009) 2016; 8
Choi, DS (WOS:000395726500006) 2017; 7
Yorita, K (WOS:A1996VU03300050) 1996; 271
Girhard, M (WOS:000249357700019) 2007; 362
(000419110500013.23) 2016; 128
Denisov, IG (WOS:000229729000010) 2005; 105
Urlacher, VB (WOS:000300077200004) 2012; 30
Girhard, M (WOS:000315100400015) 2013; 60
Churakova, E (WOS:000297175600045) 2011; 50
Biermann, U. (000419110500013.3) 2011; 123
Van Bogaert, INA (WOS:000285877700004) 2011; 278
Shoji, O (WOS:000336310000005) 2014; 19
Seiler, CY (WOS:000331139800183) 2014; 42
Philp, JC (WOS:000317457900003) 2013; 31
(000419110500013.6) 2011; 123
Kim, S (WOS:000390718900026) 2016; 42
Okita, RT (WOS:000170333100003) 2001; 2
Fujishiro, T (WOS:000294046600053) 2011; 286
References_xml – volume: 138
  start-page: 8372
  year: 2016
  publication-title: J. Am. Chem. Soc.
– volume: 18
  start-page: 2981
  year: 2016
  publication-title: Green Chem.
– volume: 139
  start-page: 12994
  year: 2017
  publication-title: J. Am. Chem. Soc.
– volume: 139
  start-page: 1061
  year: 2017
  publication-title: J. Am. Chem. Soc.
– volume: 55 128
  start-page: 6275 6383
  year: 2016 2016
  publication-title: Angew. Chem. Int. Ed. Angew. Chem.
– volume: 132
  start-page: 10955
  year: 2010
  publication-title: J. Am. Chem. Soc.
– start-page: 409
  year: 2011
  end-page: 475
– volume: 7
  start-page: 11129
  year: 2016
  publication-title: Nat. Commun.
– volume: 47 120
  start-page: 3219 3263
  year: 2008 2008
  publication-title: Angew. Chem. Int. Ed. Angew. Chem.
– volume: 10
  start-page: 1392
  year: 2015
  publication-title: ChemMedChem
– volume: 56 129
  start-page: 7242 7348
  year: 2017 2017
  publication-title: Angew. Chem. Int. Ed. Angew. Chem.
– volume: 139
  start-page: 12161
  year: 2017
  publication-title: J. Am. Chem. Soc.
– volume: 53
  start-page: 3899
  year: 2010
  publication-title: J. Med. Chem.
– volume: 115
  start-page: 3468
  year: 2015
  publication-title: Chem. Rev.
– volume: 139
  start-page: 13929
  year: 2017
  publication-title: J. Am. Chem. Soc.
– volume: 128
  start-page: 2780
  year: 2006
  publication-title: J. Am. Chem. Soc.
– volume: 6
  start-page: 488
  year: 2011
  publication-title: ChemMedChem
– volume: 138
  start-page: 12779
  year: 2016
  publication-title: J. Am. Chem. Soc.
– volume: 45
  start-page: 864
  year: 2012
  publication-title: Acc. Chem. Res.
– volume: 130
  start-page: 14052
  year: 2008
  publication-title: J. Am. Chem. Soc.
– volume: 129
  start-page: 2248
  year: 2007
  publication-title: J. Am. Chem. Soc.
– volume: 35
  start-page: 826
  year: 2002
  publication-title: Acc. Chem. Res.
– volume: 31
  start-page: 8200
  year: 2012
  publication-title: Organometallics
– volume: 132
  start-page: 10209
  year: 2010
  publication-title: J. Am. Chem. Soc.
– volume: 45
  start-page: 2
  year: 2016
  publication-title: Chem. Lett.
– volume: 4
  start-page: 2405
  year: 1998
  publication-title: Chem. Eur. J.
– volume: 39
  start-page: 2411
  year: 1996
  publication-title: J. Med. Chem.
– volume: 129
  start-page: 14193
  year: 2007
  publication-title: J. Am. Chem. Soc.
– volume: 117
  start-page: 9333
  year: 2017
  publication-title: Chem. Rev.
– volume: 135
  start-page: 9083
  year: 2013
  publication-title: J. Am. Chem. Soc.
– volume: 28
  start-page: 3552
  year: 2009
  publication-title: Organometallics
– volume: 138
  start-page: 2957
  year: 2016
  publication-title: J. Am. Chem. Soc.
– ident: e_1_2_2_10_2
  doi: 10.1021/acs.chemrev.6b00574
– ident: e_1_2_2_13_2
  doi: 10.1002/anie.200705317
– ident: e_1_2_2_35_2
  doi: 10.1021/om300819d
– ident: e_1_2_2_17_3
  doi: 10.1002/ange.201703400
– ident: e_1_2_2_25_2
  doi: 10.1021/ja805296k
– ident: e_1_2_2_27_2
  doi: 10.1039/C6GC00549G
– ident: e_1_2_2_16_2
  doi: 10.1021/jacs.6b04566
– ident: e_1_2_2_32_2
  doi: 10.1021/ja4034999
– ident: e_1_2_2_24_2
  doi: 10.1021/ja0693183
– ident: e_1_2_2_15_3
  doi: 10.1002/ange.201511975
– ident: e_1_2_2_9_2
  doi: 10.1246/cl.150913
– ident: e_1_2_2_5_2
  doi: 10.1002/cmdc.201500069
– ident: e_1_2_2_33_1
  doi: 10.1021/ar200206a
– ident: e_1_2_2_37_1
  doi: 10.1021/jacs.7b04973
– ident: e_1_2_2_34_1
– ident: e_1_2_2_13_3
  doi: 10.1002/ange.200705317
– ident: e_1_2_2_23_2
  doi: 10.1021/ja057654y
– ident: e_1_2_2_7_2
  doi: 10.1021/ar960318p
– ident: e_1_2_2_11_1
– ident: e_1_2_2_17_2
  doi: 10.1002/anie.201703400
– ident: e_1_2_2_19_2
  doi: 10.1021/jacs.6b08507
– ident: e_1_2_2_3_2
  doi: 10.1021/jm901446n
– ident: e_1_2_2_20_2
  doi: 10.1021/jacs.6b11962
– ident: e_1_2_2_21_2
  doi: 10.1021/jacs.7b08064
– ident: e_1_2_2_36_2
  doi: 10.1021/jacs.7b07637
– ident: e_1_2_2_38_1
  doi: 10.1021/om900045p
– ident: e_1_2_2_12_2
  doi: 10.1021/ja076746f
– ident: e_1_2_2_22_1
– ident: e_1_2_2_30_1
– ident: e_1_2_2_26_2
  doi: 10.1021/ja104505t
– ident: e_1_2_2_18_2
  doi: 10.1038/ncomms11129
– ident: e_1_2_2_4_2
  doi: 10.1002/cmdc.201000456
– ident: e_1_2_2_29_1
  doi: 10.1002/(SICI)1521-3765(19981204)4:12<2405::AID-CHEM2405>3.0.CO;2-0
– ident: e_1_2_2_31_2
  doi: 10.1021/jm9502293
– ident: e_1_2_2_2_1
– ident: e_1_2_2_6_1
– ident: e_1_2_2_14_2
  doi: 10.1021/ja105010t
– ident: e_1_2_2_8_2
  doi: 10.1021/cr500610p
– ident: e_1_2_2_15_2
  doi: 10.1002/anie.201511975
– ident: e_1_2_2_28_2
  doi: 10.1021/jacs.6b00024
– start-page: 409
  volume-title: Science of Synthesis, Vol. 1
  year: 2011
  ident: e_1_2_2_1_1
– volume: 8
  start-page: 2630
  year: 2016
  ident: WOS:000386916400009
  article-title: Enzymatic Resolution by a D-Lactate Oxidase Catalyzed Reaction for (S)-2-Hydroxycarboxylic Acids
  publication-title: CHEMCATCHEM
  doi: 10.1002/cctc.201600536
– volume: 30
  start-page: 26
  year: 2012
  ident: WOS:000300077200004
  article-title: Cytochrome P450 monooxygenases: an update on perspectives for synthetic application
  publication-title: TRENDS IN BIOTECHNOLOGY
  doi: 10.1016/j.tibtech.2011.06.012
– volume: 34
  start-page: 841
  year: 1999
  ident: WOS:000082583500009
  article-title: Characterization of the ybdT gene product of Bacillus subtilis:: Novel fatty acid β-hydroxylating cytochrome P450
  publication-title: LIPIDS
– volume: 50
  start-page: 10716
  year: 2011
  ident: WOS:000297175600045
  article-title: Specific Photobiocatalytic Oxyfunctionalization Reactions
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201105308
– volume: 50
  start-page: 3854
  year: 2011
  ident: WOS:000289514100007
  article-title: Oils and Fats as Renewable Raw Materials in Chemistry
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201002767
– volume: 7
  start-page: 1563
  year: 2017
  ident: WOS:000395726500006
  article-title: Photoelectroenzymatic Oxyfunctionalization on Flavin-Hybridized Carbon Nanotube Electrode Platform
  publication-title: ACS CATALYSIS
  doi: 10.1021/acscatal.6b03453
– volume: 138
  start-page: 6786
  year: 2016
  ident: WOS:000377151400017
  article-title: Emergence of Function in P450-Proteins: A Combined Quantum Mechanical/Molecular Mechanical and Molecular Dynamics Study of the Reactive Species in the H2O2-Dependent Cytochrome P450SPα and Its Regio- and Enantioselective Hydroxylation of Fatty Acids
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.6b01716
– volume: 42
  start-page: 206
  year: 2016
  ident: WOS:000390718900026
  article-title: Engineered fatty acid catabolism for fuel and chemical production
  publication-title: CURRENT OPINION IN BIOTECHNOLOGY
  doi: 10.1016/j.copbio.2016.07.004
– start-page: 69
  year: 2015
  ident: 000419110500013.7
  publication-title: Cytochrome P450
– volume: 31
  start-page: 219
  year: 2013
  ident: WOS:000317457900003
  article-title: Biobased chemicals: the convergence of green chemistry with industrial biotechnology
  publication-title: TRENDS IN BIOTECHNOLOGY
  doi: 10.1016/j.tibtech.2012.12.007
– volume: 286
  start-page: 29941
  year: 2011
  ident: WOS:000294046600053
  article-title: Crystal Structure of H2O2-dependent Cytochrome P450SPα with Its Bound Fatty Acid Substrate INSIGHT INTO THE REGIOSELECTIVE HYDROXYLATION OF FATTY ACIDS AT THE α POSITION
  publication-title: JOURNAL OF BIOLOGICAL CHEMISTRY
  doi: 10.1074/jbc.M111.245225
– start-page: 6848
  year: 2009
  ident: WOS:000271506700047
  article-title: Visible light-driven and chloroperoxidase-catalyzed oxygenation reactions
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/b915078a
– volume: 362
  start-page: 114
  year: 2007
  ident: WOS:000249357700019
  article-title: Cytochrome P450 monooxygenase from Clostridium acetobutylicum:: A new α-fatty acid hydroxylase
  publication-title: BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
  doi: 10.1016/j.bbrc.2007.07.155
– volume: 2
  start-page: 647
  year: 2012
  ident: WOS:000302387600022
  article-title: Tuning P450 Enzymes as Oxidation Catalysts
  publication-title: ACS CATALYSIS
  doi: 10.1021/cs300001x
– volume: 128
  start-page: 809
  year: 2016
  ident: 000419110500013.23
  publication-title: Angew. Chem.
– volume: 38
  start-page: 140
  year: 2013
  ident: WOS:000316243400004
  article-title: What makes a P450 tick?
  publication-title: TRENDS IN BIOCHEMICAL SCIENCES
  doi: 10.1016/j.tibs.2012.11.006
– volume: 54
  start-page: 8819
  year: 2015
  ident: WOS:000358051600046
  article-title: Oxidative Decarboxylation of Short-Chain Fatty Acids to 1-Alkenes
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201502925
– volume: 6
  start-page: 583
  year: 2004
  ident: WOS:000221735200013
  article-title: First asymmetric electroenzymatic oxidation catalyzed by a peroxidase
  publication-title: ELECTROCHEMISTRY COMMUNICATIONS
  doi: 10.1016/S1388-2481(04)00084-0
– volume: 72
  start-page: 1255
  year: 2000
  ident: WOS:000165247200007
  article-title: Fats and oils as oleochemical raw materials
  publication-title: PURE AND APPLIED CHEMISTRY
– volume: 110
  start-page: 932
  year: 2010
  ident: WOS:000274705900011
  article-title: Hydrocarbon Hydroxylation by Cytochrome P450 Enzymes
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/cr9002193
– volume: 123
  start-page: 3938
  year: 2011
  ident: 000419110500013.3
  article-title: Fette und Ole als nachwachsende Rohstoffe in der Chemie
  publication-title: Angew. Chem
– volume: 19
  start-page: 529
  year: 2014
  ident: WOS:000336310000005
  article-title: Peroxygenase reactions catalyzed by cytochromes P450
  publication-title: JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY
  doi: 10.1007/s00775-014-1106-9
– volume: 55
  start-page: 798
  year: 2016
  ident: WOS:000368069200064
  article-title: Peroxygenase-Catalyzed Oxyfunctionalization Reactions Promoted by the Complete Oxidation of Methanol
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201507881
– volume: 2
  start-page: 265
  year: 2001
  ident: WOS:000170333100003
  article-title: Cytochrome P450 4A fatty acid omega hydroxylases
  publication-title: CURRENT DRUG METABOLISM
– volume: 118
  start-page: 270
  year: 2018
  ident: WOS:000419999700007
  article-title: Artificial Biocatalytic Linear Cascades for Preparation of Organic Molecules
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/acs.chemrev.7b00033
– volume: 278
  start-page: 206
  year: 2011
  ident: WOS:000285877700004
  article-title: The role of cytochrome P450 monooxygenases in microbial fatty acid metabolism
  publication-title: FEBS JOURNAL
  doi: 10.1111/j.1742-4658.2010.07949.x
– volume: 105
  start-page: 2253
  year: 2005
  ident: WOS:000229729000010
  article-title: Structure and chemistry of cytochrome P450
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/cr0307143
– volume: 123
  start-page: 10904
  year: 2011
  ident: 000419110500013.6
  publication-title: Angew. Chem.
– volume: 124
  start-page: 128
  year: 2006
  ident: WOS:000238620900011
  article-title: Cytochromes P450 as versatile biocatalysts
  publication-title: JOURNAL OF BIOTECHNOLOGY
  doi: 10.1016/j.jbiotec.2006.01.026
– volume: 42
  start-page: D1253
  year: 2014
  ident: WOS:000331139800183
  article-title: DNASU plasmid and PSI: Biology-Materials repositories: resources to accelerate biological research
  publication-title: NUCLEIC ACIDS RESEARCH
  doi: 10.1093/nar/gkt1060
– volume: 127
  start-page: 8943
  year: 2015
  ident: 000419110500013.10
  publication-title: Angew. Chem.
– volume: 60
  start-page: 111
  year: 2013
  ident: WOS:000315100400015
  article-title: Light-driven biocatalysis with cytochrome P450 peroxygenases
  publication-title: BIOTECHNOLOGY AND APPLIED BIOCHEMISTRY
  doi: 10.1002/bab.1063
– volume: 22
  start-page: 5692
  year: 2014
  ident: WOS:000343271900020
  article-title: In situ formation of H2O2 for P450 peroxygenases
  publication-title: BIOORGANIC & MEDICINAL CHEMISTRY
  doi: 10.1016/j.bmc.2014.05.074
– volume: 77
  start-page: 1718
  year: 2011
  ident: WOS:000287700100023
  article-title: Terminal Olefin (1-Alkene) Biosynthesis by a Novel P450 Fatty Acid Decarboxylase from Jeotgalicoccus Species
  publication-title: APPLIED AND ENVIRONMENTAL MICROBIOLOGY
  doi: 10.1128/AEM.02580-10
– volume: 386
  start-page: 252
  year: 1996
  ident: WOS:A1996UM44200035
  article-title: Direct involvement of hydrogen peroxide in bacterial alpha-hydroxylation of fatty acid
  publication-title: FEBS LETTERS
– volume: 271
  start-page: 28300
  year: 1996
  ident: WOS:A1996VU03300050
  article-title: Conversion of L-lactate oxidase to a long chain alpha-hydroxyacid oxidase by site-directed mutagenesis of alanine 95 to glycine
  publication-title: JOURNAL OF BIOLOGICAL CHEMISTRY
– volume: 85
  start-page: 2263
  year: 1963
  ident: WOS:A19633102B00025
  article-title: KINETICS AND MECHANISM OF SPONTANEOUS DECOMPOSITIONS OF SOME PEROXOACIDS, HYDROGEN PEROXIDE AND T-BUTYL HYDROPEROXIDE
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
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Snippet A Ni‐catalyzed hydroarylation of styrenes and 1,3‐dienes with organoboron compounds has been developed. The reaction offers a highly selective approach to...
A Ni-catalyzed hydroarylation of styrenes and 1,3-dienes with organoboron compounds has been developed. The reaction offers a highly selective approach to...
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SubjectTerms alkenes
Chemistry
Chemistry, Multidisciplinary
coupling reactions
Dienes
hydroarylation
Nickel
Nickel compounds
Organoboron compounds
organoboron reagents
Physical Sciences
Retinoic acid
Science & Technology
Styrenes
Title Nickel(0)‐Catalyzed Hydroarylation of Styrenes and 1,3‐Dienes with Organoboron Compounds
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fanie.201710735
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=FullRecord&UT=000419110500013
https://www.ncbi.nlm.nih.gov/pubmed/29159912
https://www.proquest.com/docview/1983885540
https://www.proquest.com/docview/1966981896
Volume 57
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