Aerobic α‐Oxidation of N‐Substituted Tetrahydroisoquinolines to Dihydroisoquinolones via Organo‐photocatalysis

An efficient visible‐light‐induced α‐oxidation of N‐substituted tetrahydroisoquinolines to dihydroisoquinolones has been developed using eosin Y as an organo‐photocatalyst and oxygen as a green oxidant. The reactions were carried out under mild reaction conditions; the desired dihydroisoquinolones w...

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Published inAdvanced synthesis & catalysis Vol. 361; no. 5; pp. 1124 - 1129
Main Authors Aganda, Kim Christopher C., Hong, Boseok, Lee, Anna
Format Journal Article
LanguageEnglish
Published WEINHEIM Wiley 05.03.2019
Wiley Subscription Services, Inc
Subjects
aerobic oxidation
Chemistry
Chemistry, Applied
Chemistry, Organic
dihydroisoquinolones
lactams
Oxidation
Photocatalysis
photoredox catalysis
Physical Sciences
Science & Technology
Substitutes
Substrates
SUPPORTED GOLD NANOPARTICLES
TERTIARY-AMINES
aerobic oxidation
C-H FUNCTIONALIZATION
dihydroisoquinolones
BENZYLIC AMINES
lactams
VISIBLE-LIGHT
SYNTHETIC APPLICATIONS
photoredox catalysis
BOND ACTIVATION
EFFICIENT
CYCLIC AMINES
MOLECULAR-OXYGEN
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Abstract An efficient visible‐light‐induced α‐oxidation of N‐substituted tetrahydroisoquinolines to dihydroisoquinolones has been developed using eosin Y as an organo‐photocatalyst and oxygen as a green oxidant. The reactions were carried out under mild reaction conditions; the desired dihydroisoquinolones were obtained in up to 96% yield at room temperature under oxygen atmosphere. This transformation provides a convenient route to dihydroisoquinolones with a wide range of substrates.
AbstractList An efficient visible‐light‐induced α‐oxidation of N‐substituted tetrahydroisoquinolines to dihydroisoquinolones has been developed using eosin Y as an organo‐photocatalyst and oxygen as a green oxidant. The reactions were carried out under mild reaction conditions; the desired dihydroisoquinolones were obtained in up to 96% yield at room temperature under oxygen atmosphere. This transformation provides a convenient route to dihydroisoquinolones with a wide range of substrates.
An efficient visible-light-induced alpha-oxidation of N-substituted tetrahydroisoquinolines to dihydroisoquinolones has been developed using eosin Y as an organo-photocatalyst and oxygen as a green oxidant. The reactions were carried out under mild reaction conditions; the desired dihydroisoquinolones were obtained in up to 96% yield at room temperature under oxygen atmosphere. This transformation provides a convenient route to dihydroisoquinolones with a wide range of substrates.
Abstract An efficient visible‐light‐induced α‐oxidation of N ‐substituted tetrahydroisoquinolines to dihydroisoquinolones has been developed using eosin Y as an organo‐photocatalyst and oxygen as a green oxidant. The reactions were carried out under mild reaction conditions; the desired dihydroisoquinolones were obtained in up to 96% yield at room temperature under oxygen atmosphere. This transformation provides a convenient route to dihydroisoquinolones with a wide range of substrates. magnified image
Author Lee, Anna
Aganda, Kim Christopher C.
Hong, Boseok
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  surname: Lee
  fullname: Lee, Anna
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  organization: Myongji University
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Cites_doi 10.1016/j.tetlet.2015.01.118
10.1021/jm030086h
10.1002/adsc.201000092
10.1002/cctc.201100372
10.1021/acs.chemrev.5b00547
10.1021/ja402479r
10.1021/acs.jmedchem.6b01468
10.1021/acs.orglett.7b00021
10.1039/c6cc02452a
10.1002/anie.200700604
10.1021/acs.joc.6b00097
10.1002/chem.201604750
10.1002/anie.201602695
10.1021/acscatal.8b01897
10.1002/cctc.201402704
10.1021/jo501316m
10.1021/acs.orglett.7b03901
10.1002/asia.200900261
10.1016/j.tetlet.2016.08.073
10.1016/j.electacta.2013.10.093
10.1021/cr030692k
10.1039/c001209b
10.1039/c3gc42135j
10.3987/COM-12-S(N)71
10.1021/cs200120c
10.1021/acs.joc.7b01841
10.1016/j.tetlet.2009.02.174
10.1002/chem.201204572
10.1016/j.brainres.2005.04.039
10.1021/ja500026m
10.1002/adsc.201501007
10.1007/s10562-016-1834-2
10.1039/c6ra25469a
10.1021/ol202857t
10.1039/c2gc36683e
10.1002/anie.200300630
10.1021/acs.orglett.7b01230
10.1021/acs.accounts.7b00108
10.1055/s-0032-1316747
10.1039/c7gc03741d
10.1055/s-0030-1259937
10.1016/j.tetlet.2015.10.048
10.1021/ol201376v
10.1039/c4gc01321b
10.1021/acs.chemrev.7b00193
10.1016/j.tetlet.2009.01.010
10.1246/bcsj.20100300
10.1021/acs.jmedchem.5b01607
10.1021/ed100457z
10.1016/S0010-8545(02)00034-6
10.1039/C4GC01321B
10.1039/C6CC02452A
10.1055/s-0031-1289761
10.1039/C6RA25469A
10.1039/C7GC03741D
10.1016/S0040-4020(02)00573-2
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Keywords SUPPORTED GOLD NANOPARTICLES
TERTIARY-AMINES
aerobic oxidation
C-H FUNCTIONALIZATION
dihydroisoquinolones
BENZYLIC AMINES
lactams
VISIBLE-LIGHT
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photoredox catalysis
BOND ACTIVATION
EFFICIENT
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MOLECULAR-OXYGEN
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References 2004; 43
2015; 56
2002; 58
2017; 7
2004; 104
2017; 60
2017; 82
2011; 1
2011
2008; 16
2011; 84
2017; 23
2016; 146
2016; 52
2011; 13
2012; 14
2018; 20
2016; 59
2015; 7
2014; 136
2016; 57
2016; 55
2013; 19
2002; 233–234
2017; 50
2011; 2011
2010; 87
2018; 8
2013; 15
2010; 46
2009; 50
2018; 118
2008; 47
2014; 16
2003; 46
2010; 352
2013; 114
2014; 79
2013; 135
2017; 19
2016; 358
2016; 116
2016; 81
2009; 4
2012; 4
2005; 1049
2012; 44
2012; 86
Asano, Y. (000461675600028.2) 2008; 16
Miyamura, H (WOS:000292535300002) 2011; 84
Liu, X (WOS:000381847600044) 2016; 81
Zhang, LL (WOS:000412789000079) 2017; 82
DeRosa, MC (WOS:000178841400021) 2002; 233
Dad'ova, J (WOS:000303151500006) 2012; 4
Kohls, P (WOS:000300458200002) 2012; 14
Khusnutdinova, JR (WOS:000332144300017) 2014; 136
Liang, YJ (WOS:000433404300002) 2018; 118
Stahl, SS (WOS:000222428800004) 2004; 43
Mohamed, MA (WOS:000267070700085) 2009; 50
Kim, DH (WOS:000424729800068) 2018; 20
Renaud, J (WOS:000183824500014) 2003; 46
Ratnikov, MO (WOS:000321236600047) 2013; 135
Dairo, TO (WOS:000387325300008) 2016; 146
Wu, XF (WOS:000371663600001) 2016; 358
Chrzanowska, M (WOS:000222769100005) 2004; 104
Finney, LC (WOS:000435867600008) 2018; 20
Song, AR (WOS:000308866800012) 2012; 44
Klobukowski, ER (WOS:000292479400005) 2011; 1
Gu, XY (WOS:000314185900011) 2013; 15
Yadav, AK (WOS:000365060400011) 2015; 56
Amaya, T (WOS:000314390600005) 2012; 86
Chatterjee, N (WOS:000351247600014) 2015; 56
Liu, P (WOS:000276376000007) 2010; 46
Borthwick, JA (WOS:000372946500013) 2016; 59
Hudlicky, M. (000461675600028.20) 1990; 186
Jin, XJ (WOS:000382790600034) 2016; 55
Kim, J (WOS:000263749600019) 2009; 50
So, MH (WOS:000270768000007) 2009; 4
(000461675600028.1) 1967
Li, C (WOS:000330487800075) 2013; 114
Jin, RW (WOS:000347781400002) 2015; 7
Bechi, B (WOS:000342885900008) 2014; 16
Pandey, G (WOS:000383939900009) 2016; 57
Casado-Sanchez, A (WOS:000379431000039) 2016; 52
Burks, HE (WOS:000399436100013) 2017; 60
Liu, YX (WOS:000395774700013) 2017; 23
Yoshimura, A (WOS:000371947300010) 2016; 116
Griffiths, RJ (WOS:000394736300033) 2017; 19
Shibley, IA (WOS:000284033000020) 2010; 87
Chen, KX (WOS:000335005200002) 2014; 16
Piera, J (WOS:000255530100007) 2008; 47
Briet, N (WOS:000176846600001) 2002; 58
Yang, SA (WOS:000405358300014) 2017; 19
Zhang, YB (WOS:000395935300026) 2017; 7
Lorenc-Koci, E (WOS:000231345000001) 2005; 1049
Liang, YF (WOS:000406085500016) 2017; 50
Preedasuriyachai, P (WOS:000290206600014) 2011
Hari, DP (WOS:000293252800022) 2011; 13
Liu, J (WOS:000340517600033) 2014; 79
Han, W (WOS:000280657900019) 2010; 352
Zhang, Y (WOS:000438475100104) 2018; 8
Zhong, JJ (WOS:000318365200034) 2013; 19
e_1_2_2_24_2
e_1_2_2_47_2
e_1_2_2_4_2
e_1_2_2_6_1
e_1_2_2_22_2
e_1_2_2_49_2
e_1_2_2_20_2
e_1_2_2_2_1
Preedasuriyachai P. (e_1_2_2_45_2) 2011
e_1_2_2_62_2
e_1_2_2_41_2
e_1_2_2_64_2
e_1_2_2_8_2
e_1_2_2_28_2
e_1_2_2_43_2
e_1_2_2_66_2
e_1_2_2_26_2
e_1_2_2_68_2
e_1_2_2_60_2
e_1_2_2_13_2
e_1_2_2_38_1
e_1_2_2_59_1
e_1_2_2_11_2
e_1_2_2_51_1
e_1_2_2_19_2
e_1_2_2_30_2
e_1_2_2_53_2
e_1_2_2_17_2
e_1_2_2_32_2
e_1_2_2_55_2
e_1_2_2_34_1
e_1_2_2_15_2
e_1_2_2_57_2
e_1_2_2_36_1
Asano Y. (e_1_2_2_40_2) 2008; 16
e_1_2_2_3_2
e_1_2_2_5_1
e_1_2_2_23_2
e_1_2_2_48_2
e_1_2_2_69_2
e_1_2_2_21_1
e_1_2_2_63_1
e_1_2_2_61_2
e_1_2_2_42_1
e_1_2_2_7_2
e_1_2_2_9_1
e_1_2_2_29_1
e_1_2_2_67_1
e_1_2_2_27_2
e_1_2_2_44_2
e_1_2_2_65_2
e_1_2_2_25_2
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e_1_2_2_14_1
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e_1_2_2_12_2
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e_1_2_2_10_2
e_1_2_2_39_2
e_1_2_2_18_2
e_1_2_2_31_2
e_1_2_2_52_2
e_1_2_2_16_2
e_1_2_2_33_2
e_1_2_2_54_2
e_1_2_2_35_1
e_1_2_2_56_2
e_1_2_2_50_1
References_xml – volume: 84
  start-page: 588
  year: 2011
  publication-title: Bull. Chem. Soc. Jpn.
– volume: 23
  start-page: 3062
  year: 2017
  publication-title: Chem. Eur. J.
– volume: 86
  start-page: 927
  year: 2012
  publication-title: Heterocycles
– volume: 19
  start-page: 6443
  year: 2013
  publication-title: Chem. Eur. J.
– volume: 56
  start-page: 1524
  year: 2015
  publication-title: Tetrahedron Lett.
– start-page: 1121
  year: 2011
  publication-title: Synlett
– volume: 16
  start-page: 4524
  year: 2014
  publication-title: Green Chem.
– volume: 4
  start-page: 620
  year: 2012
  publication-title: ChemCatChem
– volume: 4
  start-page: 1551
  year: 2009
  publication-title: Chem. Asian J.
– volume: 358
  start-page: 336
  year: 2016
  publication-title: Adv. Synth. Catal.
– volume: 116
  start-page: 3328
  year: 2016
  publication-title: Chem. Rev.
– volume: 46
  start-page: 2739
  year: 2010
  publication-title: Chem. Commun.
– volume: 55
  start-page: 7212
  year: 2016
  publication-title: Angew. Chem. Int. Ed.
– volume: 59
  start-page: 2452
  year: 2016
  publication-title: J. Med. Chem.
– volume: 50
  start-page: 1640
  year: 2017
  publication-title: Acc. Chem. Res.
– volume: 81
  start-page: 7256
  year: 2016
  publication-title: J. Org. Chem.
– volume: 1
  start-page: 703
  year: 2011
  publication-title: ACS Catal.
– volume: 104
  start-page: 3341
  year: 2004
  publication-title: Chem. Rev.
– volume: 19
  start-page: 3386
  year: 2017
  publication-title: Org. Lett.
– volume: 52
  start-page: 9137
  year: 2016
  publication-title: Chem. Commun.
– volume: 135
  start-page: 9475
  year: 2013
  publication-title: J. Am. Chem. Soc.
– volume: 19
  start-page: 870
  year: 2017
  publication-title: Org. Lett.
– volume: 87
  start-page: 1351
  year: 2010
  publication-title: J. Chem. Educ.
– volume: 79
  start-page: 7593
  year: 2014
  publication-title: J. Org. Chem.
– volume: 16
  start-page: 4175
  year: 2008
  publication-title: Bioorg. Med. Chem.
– volume: 15
  start-page: 357
  year: 2013
  publication-title: Green Chem.
– volume: 14
  start-page: 672
  year: 2012
  publication-title: Org. Lett.
– volume: 57
  start-page: 4480
  year: 2016
  publication-title: Tetrahedron Lett.
– volume: 146
  start-page: 2278
  year: 2016
  publication-title: Catal. Lett.
– volume: 20
  start-page: 2242
  year: 2018
  publication-title: Green Chem.
– volume: 7
  start-page: 223
  year: 2015
  publication-title: ChemCatChem
– volume: 44
  start-page: 2903
  year: 2012
  publication-title: Synthesis
– volume: 1049
  start-page: 133
  year: 2005
  publication-title: Brain Res.
– volume: 50
  start-page: 3436
  year: 2009
  publication-title: Tetrahedron Lett.
– volume: 13
  start-page: 3852
  year: 2011
  publication-title: Org. Lett.
– volume: 60
  start-page: 2790
  year: 2017
  publication-title: J. Med. Chem.
– volume: 114
  start-page: 560
  year: 2013
  publication-title: Electrochim. Acta
– volume: 8
  start-page: 6659
  year: 2018
  publication-title: ACS Catal.
– volume: 20
  start-page: 764
  year: 2018
  publication-title: Org. Lett.
– volume: 352
  start-page: 1667
  year: 2010
  publication-title: Adv. Synth. Catal.
– volume: 56
  start-page: 6696
  year: 2015
  publication-title: Tetrahedron Lett.
– volume: 43
  start-page: 3400
  year: 2004
  publication-title: Angew. Chem. Int. Ed.
– volume: 233–234
  start-page: 351
  year: 2002
  publication-title: Coord. Chem. Rev.
– volume: 7
  start-page: 13240
  year: 2017
  publication-title: RSC Adv.
– volume: 82
  start-page: 10704
  year: 2017
  publication-title: J. Org. Chem.
– volume: 47
  start-page: 3506
  year: 2008
  publication-title: Angew. Chem. Int. Ed.
– volume: 118
  start-page: 4912
  year: 2018
  publication-title: Chem. Rev.
– volume: 58
  start-page: 5761
  year: 2002
  publication-title: Tetrahedron
– volume: 50
  start-page: 1229
  year: 2009
  publication-title: Tetrahedron Lett.
– volume: 136
  start-page: 2998
  year: 2014
  publication-title: J. Am. Chem. Soc.
– volume: 16
  start-page: 2344
  year: 2014
  publication-title: Green Chem.
– volume: 46
  start-page: 2945
  year: 2003
  publication-title: J. Med. Chem.
– volume: 2011
  start-page: 1121
  year: 2011
  publication-title: Synlett
– volume: 56
  start-page: 1524
  year: 2015
  ident: WOS:000351247600014
  article-title: Organic hypervalent iodine(III) catalyzed ipso-hydroxylation of aryl- and alkylboronic acids/esters
  publication-title: TETRAHEDRON LETTERS
  doi: 10.1016/j.tetlet.2015.01.118
  contributor:
    fullname: Chatterjee, N
– volume: 46
  start-page: 2945
  year: 2003
  ident: WOS:000183824500014
  article-title: Estrogen receptor modulators: Identification and structure-activity relationships of potent ER alpha-selective tetrahydroisoquinoline ligands
  publication-title: JOURNAL OF MEDICINAL CHEMISTRY
  doi: 10.1021/jm030086h
  contributor:
    fullname: Renaud, J
– volume: 352
  start-page: 1667
  year: 2010
  ident: WOS:000280657900019
  article-title: Iron-Catalyzed Oxidative Mono- and Bis-Phosphonation of N,N-Dialkylanilines
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201000092
  contributor:
    fullname: Han, W
– volume: 4
  start-page: 620
  year: 2012
  ident: WOS:000303151500006
  article-title: Photooxidation of Sulfides to Sulfoxides Mediated by Tetra-O-Acetylriboflavin and Visible Light
  publication-title: CHEMCATCHEM
  doi: 10.1002/cctc.201100372
  contributor:
    fullname: Dad'ova, J
– volume: 116
  start-page: 3328
  year: 2016
  ident: WOS:000371947300010
  article-title: Advances in Synthetic Applications of Hypervalent Iodine Compounds
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/acs.chemrev.5b00547
  contributor:
    fullname: Yoshimura, A
– volume: 135
  start-page: 9475
  year: 2013
  ident: WOS:000321236600047
  article-title: Simple and Sustainable Iron-Catalyzed Aerobic C-H Functionalization of N,N-Dialkylanilines
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja402479r
  contributor:
    fullname: Ratnikov, MO
– volume: 60
  start-page: 2790
  year: 2017
  ident: WOS:000399436100013
  article-title: Discovery of an Acrylic Acid Based Tetrahydroisoquinoline as an Orally Bioavailable Selective Estrogen Receptor Degrader for ER alpha plus Breast Cancer
  publication-title: JOURNAL OF MEDICINAL CHEMISTRY
  doi: 10.1021/acs.jmedchem.6b01468
  contributor:
    fullname: Burks, HE
– volume: 19
  start-page: 870
  year: 2017
  ident: WOS:000394736300033
  article-title: Transition-Metal-Free Amine Oxidation: A Chemoselective Strategy for the Late-Stage Formation of Lactams
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.7b00021
  contributor:
    fullname: Griffiths, RJ
– volume: 52
  start-page: 9137
  year: 2016
  ident: WOS:000379431000039
  article-title: Pt(II) coordination complexes as visible light photocatalysts for the oxidation of sulfides using batch and flow processes
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c6cc02452a
  contributor:
    fullname: Casado-Sanchez, A
– volume: 47
  start-page: 3506
  year: 2008
  ident: WOS:000255530100007
  article-title: Catalytic oxidation of organic substrates by molecular oxygen and hydrogen peroxide by multistep electron transfer - A biomimetic approach
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.200700604
  contributor:
    fullname: Piera, J
– volume: 16
  start-page: 4175
  year: 2008
  ident: 000461675600028.2
  publication-title: Bioorg. Med. Chem.
  contributor:
    fullname: Asano, Y.
– volume: 81
  start-page: 7256
  year: 2016
  ident: WOS:000381847600044
  article-title: Synthesis of 1,2-Diketones via a Metal-Free, Visible-Light-Induced Aerobic Photooxidation of Alkynes
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/acs.joc.6b00097
  contributor:
    fullname: Liu, X
– volume: 23
  start-page: 3062
  year: 2017
  ident: WOS:000395774700013
  article-title: Reactions Catalysed by a Binuclear Copper Complex: Relay Aerobic Oxidation of N-Aryl Tetrahydroisoquinolines to Dihydroisoquinolones with a Vitamin B1 Analogue
  publication-title: CHEMISTRY-A EUROPEAN JOURNAL
  doi: 10.1002/chem.201604750
  contributor:
    fullname: Liu, YX
– volume: 55
  start-page: 7212
  year: 2016
  ident: WOS:000382790600034
  article-title: Supported Gold Nanoparticles for Efficient alpha-Oxygenation of Secondary and Tertiary Amines into Amides
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201602695
  contributor:
    fullname: Jin, XJ
– volume: 233
  start-page: 351
  year: 2002
  ident: WOS:000178841400021
  article-title: Photosensitized singlet oxygen and its applications
  publication-title: COORDINATION CHEMISTRY REVIEWS
  contributor:
    fullname: DeRosa, MC
– volume: 8
  start-page: 6659
  year: 2018
  ident: WOS:000438475100104
  article-title: Visible-Light-Mediated Efficient Metal-Free Catalyst for alpha-Oxygenation of Tertiary Amines to Amides
  publication-title: ACS CATALYSIS
  doi: 10.1021/acscatal.8b01897
  contributor:
    fullname: Zhang, Y
– year: 1967
  ident: 000461675600028.1
– volume: 7
  start-page: 223
  year: 2015
  ident: WOS:000347781400002
  article-title: Metal-free Dehydrogenative Isoquinolone Synthesis
  publication-title: CHEMCATCHEM
  doi: 10.1002/cctc.201402704
  contributor:
    fullname: Jin, RW
– volume: 79
  start-page: 7593
  year: 2014
  ident: WOS:000340517600033
  article-title: N-Methylimidazole Promotes the Reaction of Homophthalic Anhydride with Imines
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/jo501316m
  contributor:
    fullname: Liu, J
– volume: 20
  start-page: 764
  year: 2018
  ident: WOS:000424729800068
  article-title: Visible-Light-Driven Silver-Catalyzed One-Pot Approach: A Selective Synthesis of Diaryl Sulfoxides and Diaryl Sulfones
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.7b03901
  contributor:
    fullname: Kim, DH
– volume: 4
  start-page: 1551
  year: 2009
  ident: WOS:000270768000007
  article-title: Graphite-Supported Gold Nanoparticles as Efficient Catalyst for Aerobic Oxidation of Benzylic Amines to Imines and N-Substituted 1,2,3,4-Tetrahydroisoquinolines to Amides: Synthetic Applications and Mechanistic Study
  publication-title: CHEMISTRY-AN ASIAN JOURNAL
  doi: 10.1002/asia.200900261
  contributor:
    fullname: So, MH
– volume: 57
  start-page: 4480
  year: 2016
  ident: WOS:000383939900009
  article-title: alpha-Alltylation of tertiary amines by C(sp(3))-C(sp(3)) cross-coupling under redox neutral photocatalysis
  publication-title: TETRAHEDRON LETTERS
  doi: 10.1016/j.tetlet.2016.08.073
  contributor:
    fullname: Pandey, G
– volume: 114
  start-page: 560
  year: 2013
  ident: WOS:000330487800075
  article-title: Electrochemically induced C-H functionalization using bromide ion/2,2,6,6-tetramethylpiperidinyl-N-oxyl dual redox catalysts in a two-phase electrolytic system
  publication-title: ELECTROCHIMICA ACTA
  doi: 10.1016/j.electacta.2013.10.093
  contributor:
    fullname: Li, C
– volume: 104
  start-page: 3341
  year: 2004
  ident: WOS:000222769100005
  article-title: Asymmetric synthesis of isoquinoline alkaloids
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/cr030692k
  contributor:
    fullname: Chrzanowska, M
– volume: 46
  start-page: 2739
  year: 2010
  ident: WOS:000276376000007
  article-title: Highly efficient oxidative carbon-carbon coupling with SBA-15-support iron terpyridine catalyst
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c001209b
  contributor:
    fullname: Liu, P
– volume: 16
  start-page: 2344
  year: 2014
  ident: WOS:000335005200002
  article-title: Metal-free allylic/benzylic oxidation strategies with molecular oxygen: recent advances and future prospects
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c3gc42135j
  contributor:
    fullname: Chen, KX
– volume: 86
  start-page: 927
  year: 2012
  ident: WOS:000314390600005
  article-title: SELECTIVE CROSS-DEHYDROGENATIVE COUPLING OF N-PHENYLTETRAHYDROISOQUINOLINES IN AQUEOUS MEDIA USING POLY(ANILINE SULFONIC ACID)/GOLD NANOPARTICLES
  publication-title: HETEROCYCLES
  doi: 10.3987/COM-12-S(N)71
  contributor:
    fullname: Amaya, T
– volume: 1
  start-page: 703
  year: 2011
  ident: WOS:000292479400005
  article-title: Conversions of Cyclic Amines to Nylon Precursor Lactams Using Bulk Gold and Fumed Silica Catalysts
  publication-title: ACS CATALYSIS
  doi: 10.1021/cs200120c
  contributor:
    fullname: Klobukowski, ER
– volume: 82
  start-page: 10704
  year: 2017
  ident: WOS:000412789000079
  article-title: Visible-Light Mediated Oxidative C-H/N-H Cross-Coupling between Tetrahydrofuran and Azoles Using Air
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/acs.joc.7b01841
  contributor:
    fullname: Zhang, LL
– volume: 186
  year: 1990
  ident: 000461675600028.20
  publication-title: Oxidation in Organic Chemistry
  contributor:
    fullname: Hudlicky, M.
– volume: 50
  start-page: 3436
  year: 2009
  ident: WOS:000267070700085
  article-title: Accessing the amide functionality by the mild and low-cost oxidation of imine
  publication-title: TETRAHEDRON LETTERS
  doi: 10.1016/j.tetlet.2009.02.174
  contributor:
    fullname: Mohamed, MA
– volume: 19
  start-page: 6443
  year: 2013
  ident: WOS:000318365200034
  article-title: A Highly Efficient and Selective Aerobic Cross-Dehydrogenative-Coupling Reaction Photocatalyzed by a Platinum(II) Terpyridyl Complex
  publication-title: CHEMISTRY-A EUROPEAN JOURNAL
  doi: 10.1002/chem.201204572
  contributor:
    fullname: Zhong, JJ
– volume: 1049
  start-page: 133
  year: 2005
  ident: WOS:000231345000001
  article-title: Treatment with 1,2,3,4-tetrahydroisoquinolone affects the levels of nitric oxide, S-nitrosothiols, glutathione and the enzymatic activity of gamma-glutamyl transpeptidase in the dopaminergic structures of rat brain
  publication-title: BRAIN RESEARCH
  doi: 10.1016/j.brainres.2005.04.039
  contributor:
    fullname: Lorenc-Koci, E
– volume: 136
  start-page: 2998
  year: 2014
  ident: WOS:000332144300017
  article-title: Oxidant-Free Conversion of Cyclic Amines to Lactams and H-2 Using Water As the Oxygen Atom Source
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja500026m
  contributor:
    fullname: Khusnutdinova, JR
– volume: 358
  start-page: 336
  year: 2016
  ident: WOS:000371663600001
  article-title: The Applications of Dimethyl Sulfoxide as Reagent in Organic Synthesis
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201501007
  contributor:
    fullname: Wu, XF
– volume: 58
  start-page: 5761
  year: 2002
  ident: WOS:000176846600001
  article-title: Synthesis of novel substituted isoquinolones
  publication-title: TETRAHEDRON
  contributor:
    fullname: Briet, N
– volume: 146
  start-page: 2278
  year: 2016
  ident: WOS:000387325300008
  article-title: Aerobic Oxidation of Cyclic Amines to Lactams Catalyzed by Ceria-Supported Nanogold
  publication-title: CATALYSIS LETTERS
  doi: 10.1007/s10562-016-1834-2
  contributor:
    fullname: Dairo, TO
– volume: 7
  start-page: 13240
  year: 2017
  ident: WOS:000395935300026
  article-title: Eosin Y-catalyzed photooxidation of triarylphosphines under visible light irradiation and aerobic conditions
  publication-title: RSC ADVANCES
  doi: 10.1039/c6ra25469a
  contributor:
    fullname: Zhang, YB
– volume: 14
  start-page: 672
  year: 2012
  ident: WOS:000300458200002
  article-title: Visible Light Photoredox Catalysis: Generation and Addition of N-Aryltetrahydroisoquinoline-Derived alpha-Amino Radicals to Michael Acceptors
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol202857t
  contributor:
    fullname: Kohls, P
– volume: 15
  start-page: 357
  year: 2013
  ident: WOS:000314185900011
  article-title: A simple metal-free catalytic sulfoxidation under visible light and air
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c2gc36683e
  contributor:
    fullname: Gu, XY
– volume: 43
  start-page: 3400
  year: 2004
  ident: WOS:000222428800004
  article-title: Palladium oxidase catalysis: Selective oxidation of organic chemicals by direct dioxygen-coupled turnover
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.200300630
  contributor:
    fullname: Stahl, SS
– volume: 19
  start-page: 3386
  year: 2017
  ident: WOS:000405358300014
  article-title: Photoinduced Oxidative Formylation of N,N-Dimethylanilines with Molecular Oxygen without External Photocatalyst
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.7b01230
  contributor:
    fullname: Yang, SA
– volume: 50
  start-page: 1640
  year: 2017
  ident: WOS:000406085500016
  article-title: Oxygenation via C-H/C-C Bond Activation with Molecular Oxygen
  publication-title: ACCOUNTS OF CHEMICAL RESEARCH
  doi: 10.1021/acs.accounts.7b00108
  contributor:
    fullname: Liang, YF
– volume: 44
  start-page: 2903
  year: 2012
  ident: WOS:000308866800012
  article-title: A Simple and Effective Synthesis of Benzolactones and Benzolactams by Noncatalytic Benzylic Oxidation of Cyclic Benzylic Ethers and N-Protected Cyclic Benzylic Amines with Sodium Chlorite as an Oxidant
  publication-title: SYNTHESIS-STUTTGART
  doi: 10.1055/s-0032-1316747
  contributor:
    fullname: Song, AR
– volume: 20
  start-page: 2242
  year: 2018
  ident: WOS:000435867600008
  article-title: Visible light mediated oxidation of benzylic sp(3) C-H bonds using catalytic 1,4-hydroquinone, or its biorenewable glucoside, arbutin, as a pre-oxidant
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c7gc03741d
  contributor:
    fullname: Finney, LC
– start-page: 1121
  year: 2011
  ident: WOS:000290206600014
  article-title: Aerobic Oxidation of Cyclic Amines to Lactams Catalyzed by PVP-Stabilized Nanogold
  publication-title: SYNLETT
  doi: 10.1055/s-0030-1259937
  contributor:
    fullname: Preedasuriyachai, P
– volume: 56
  start-page: 6696
  year: 2015
  ident: WOS:000365060400011
  article-title: Visible-light-induced direct alpha-C(sp(3))-H thiocyanation of tertiary amines
  publication-title: TETRAHEDRON LETTERS
  doi: 10.1016/j.tetlet.2015.10.048
  contributor:
    fullname: Yadav, AK
– volume: 13
  start-page: 3852
  year: 2011
  ident: WOS:000293252800022
  article-title: Eosin Y Catalyzed Visible Light Oxidative C-C and C-P bond Formation
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol201376v
  contributor:
    fullname: Hari, DP
– volume: 16
  start-page: 4524
  year: 2014
  ident: WOS:000342885900008
  article-title: Catalytic bio-chemo and bio-bio tandem oxidation reactions for amide and carboxylic acid synthesis
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c4gc01321b
  contributor:
    fullname: Bechi, B
– volume: 118
  start-page: 4912
  year: 2018
  ident: WOS:000433404300002
  article-title: Homogeneous Oxygenase Catalysis
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/acs.chemrev.7b00193
  contributor:
    fullname: Liang, YJ
– volume: 50
  start-page: 1229
  year: 2009
  ident: WOS:000263749600019
  article-title: Pd-catalyzed ortho-arylation of 3,4-dihydroisoquinolones via C-H bond activation: synthesis of 8-aryl-1,2,3,4-tetrahydroisoquinolines
  publication-title: TETRAHEDRON LETTERS
  doi: 10.1016/j.tetlet.2009.01.010
  contributor:
    fullname: Kim, J
– volume: 84
  start-page: 588
  year: 2011
  ident: WOS:000292535300002
  article-title: Aerobic Oxidation of Amines Catalyzed by Polymer-Incarcerated Au Nanoclusters: Effect of Cluster Size and Cooperative Functional Groups in the Polymer
  publication-title: BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN
  doi: 10.1246/bcsj.20100300
  contributor:
    fullname: Miyamura, H
– volume: 59
  start-page: 2452
  year: 2016
  ident: WOS:000372946500013
  article-title: Structurally Diverse Mitochondrial Branched Chain Aminotransferase (BCATm) Leads with Varying Binding Modes Identified by Fragment Screening
  publication-title: JOURNAL OF MEDICINAL CHEMISTRY
  doi: 10.1021/acs.jmedchem.5b01607
  contributor:
    fullname: Borthwick, JA
– volume: 87
  start-page: 1351
  year: 2010
  ident: WOS:000284033000020
  article-title: Oxidation and Reduction Reactions in Organic Chemistry
  publication-title: JOURNAL OF CHEMICAL EDUCATION
  doi: 10.1021/ed100457z
  contributor:
    fullname: Shibley, IA
– ident: e_1_2_2_23_2
  doi: 10.1021/cs200120c
– ident: e_1_2_2_36_1
  doi: 10.1016/j.brainres.2005.04.039
– ident: e_1_2_2_13_2
  doi: 10.1021/acs.chemrev.7b00193
– ident: e_1_2_2_3_2
– ident: e_1_2_2_16_2
  doi: 10.1039/c2gc36683e
– ident: e_1_2_2_68_2
  doi: 10.1016/S0010-8545(02)00034-6
– ident: e_1_2_2_38_1
– ident: e_1_2_2_43_2
  doi: 10.1016/j.tetlet.2009.02.174
– ident: e_1_2_2_57_2
  doi: 10.1021/ja402479r
– ident: e_1_2_2_29_1
– ident: e_1_2_2_58_2
  doi: 10.1002/chem.201204572
– ident: e_1_2_2_48_2
  doi: 10.1039/C4GC01321B
– ident: e_1_2_2_54_2
  doi: 10.1246/bcsj.20100300
– ident: e_1_2_2_64_2
  doi: 10.1021/ol201376v
– ident: e_1_2_2_20_2
  doi: 10.1021/acs.orglett.7b03901
– ident: e_1_2_2_18_2
  doi: 10.1039/C6CC02452A
– ident: e_1_2_2_53_2
  doi: 10.1002/adsc.201000092
– ident: e_1_2_2_14_1
– ident: e_1_2_2_56_2
  doi: 10.3987/COM-12-S(N)71
– ident: e_1_2_2_8_2
  doi: 10.1021/acs.chemrev.5b00547
– ident: e_1_2_2_7_2
  doi: 10.1016/j.tetlet.2015.01.118
– start-page: 1121
  year: 2011
  ident: e_1_2_2_45_2
  publication-title: Synlett
  contributor:
    fullname: Preedasuriyachai P.
– ident: e_1_2_2_66_2
  doi: 10.1016/j.tetlet.2016.08.073
– ident: e_1_2_2_6_1
– ident: e_1_2_2_63_1
– ident: e_1_2_2_9_1
– ident: e_1_2_2_33_2
  doi: 10.1021/acs.jmedchem.6b01468
– ident: e_1_2_2_61_2
  doi: 10.1021/acs.orglett.7b01230
– ident: e_1_2_2_15_2
  doi: 10.1002/cctc.201100372
– ident: e_1_2_2_51_1
– ident: e_1_2_2_5_1
  doi: 10.1002/adsc.201501007
– ident: e_1_2_2_35_1
– ident: e_1_2_2_47_2
  doi: 10.1016/j.electacta.2013.10.093
– volume: 16
  start-page: 4175
  year: 2008
  ident: e_1_2_2_40_2
  publication-title: Bioorg. Med. Chem.
  contributor:
    fullname: Asano Y.
– ident: e_1_2_2_42_1
– ident: e_1_2_2_25_2
  doi: 10.1021/ja500026m
– ident: e_1_2_2_60_2
  doi: 10.1021/acs.joc.6b00097
– ident: e_1_2_2_27_2
  doi: 10.1002/anie.201602695
– ident: e_1_2_2_32_2
  doi: 10.1016/j.tetlet.2009.01.010
– ident: e_1_2_2_39_2
  doi: 10.1021/jm030086h
– ident: e_1_2_2_17_2
  doi: 10.1039/c3gc42135j
– ident: e_1_2_2_41_2
  doi: 10.1002/cctc.201402704
– ident: e_1_2_2_10_2
  doi: 10.1002/anie.200300630
– ident: e_1_2_2_12_2
  doi: 10.1021/acs.accounts.7b00108
– ident: e_1_2_2_46_2
  doi: 10.1055/s-0031-1289761
– ident: e_1_2_2_31_2
  doi: 10.1021/cr030692k
– ident: e_1_2_2_55_2
  doi: 10.1021/ol202857t
– ident: e_1_2_2_65_2
  doi: 10.1016/j.tetlet.2015.10.048
– ident: e_1_2_2_28_2
  doi: 10.1002/chem.201604750
– ident: e_1_2_2_4_2
  doi: 10.1021/ed100457z
– ident: e_1_2_2_44_2
  doi: 10.1002/asia.200900261
– ident: e_1_2_2_69_2
  doi: 10.1039/C6RA25469A
– ident: e_1_2_2_19_2
  doi: 10.1039/C7GC03741D
– ident: e_1_2_2_30_2
  doi: 10.1016/S0040-4020(02)00573-2
– ident: e_1_2_2_11_2
  doi: 10.1002/anie.200700604
– ident: e_1_2_2_24_2
  doi: 10.1055/s-0030-1259937
– ident: e_1_2_2_59_1
– ident: e_1_2_2_67_1
– ident: e_1_2_2_26_2
  doi: 10.1007/s10562-016-1834-2
– ident: e_1_2_2_34_1
  doi: 10.1021/jo501316m
– ident: e_1_2_2_62_2
  doi: 10.1021/acs.joc.7b01841
– ident: e_1_2_2_2_1
– ident: e_1_2_2_37_1
  doi: 10.1021/acs.jmedchem.5b01607
– ident: e_1_2_2_22_2
  doi: 10.1002/asia.200900261
– ident: e_1_2_2_21_1
– ident: e_1_2_2_49_2
  doi: 10.1021/acs.orglett.7b00021
– ident: e_1_2_2_50_1
  doi: 10.1021/acscatal.8b01897
– ident: e_1_2_2_52_2
  doi: 10.1039/c001209b
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Snippet An efficient visible‐light‐induced α‐oxidation of N‐substituted tetrahydroisoquinolines to dihydroisoquinolones has been developed using eosin Y as an...
An efficient visible-light-induced alpha-oxidation of N-substituted tetrahydroisoquinolines to dihydroisoquinolones has been developed using eosin Y as an...
Abstract An efficient visible‐light‐induced α‐oxidation of N ‐substituted tetrahydroisoquinolines to dihydroisoquinolones has been developed using eosin Y as...
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SubjectTerms aerobic oxidation
Chemistry
Chemistry, Applied
Chemistry, Organic
dihydroisoquinolones
lactams
Oxidation
Photocatalysis
photoredox catalysis
Physical Sciences
Science & Technology
Substitutes
Substrates
Title Aerobic α‐Oxidation of N‐Substituted Tetrahydroisoquinolines to Dihydroisoquinolones via Organo‐photocatalysis
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fadsc.201801301
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