Direct synthesis of nitriles by Cu/DMEDA/TEMPO-catalyzed aerobic oxidation of primary amines with air

By screening the copper catalysts,ligands,and the reaction conditions,a simple CuCl/DMEDA/TEMPO catalyst system readily available from commercial sources is developed for a direct and selective synthesis of the useful nitriles by an aerobic oxidation reaction of primary amines using air as an advant...

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Published inChinese chemical letters Vol. 28; no. 6; pp. 1336 - 1339
Main Authors Ma, Xian-Tao, Xu, Hao, Xiao, Ying-Lin, Su, Chen-Liang, Liu, Jian-Ping, Xu, Qing
Format Journal Article
LanguageEnglish
Published NEW YORK Elsevier B.V 01.06.2017
Elsevier
Subjects
Aerobic oxidation
Air
Amines
Chemistry
Chemistry, Multidisciplinary
Copper catalysis
Nitriles
Physical Sciences
Science & Technology
Nitriles
Amines
Air
Copper catalysis
Aerobic oxidation
ROOM-TEMPERATURE
CONVERSION
IMINES
HYDRATION
ALCOHOLS
EFFICIENT CATALYST
DEHYDROGENATION
ARYL HALIDES
METAL
AMIDES
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Abstract By screening the copper catalysts,ligands,and the reaction conditions,a simple CuCl/DMEDA/TEMPO catalyst system readily available from commercial sources is developed for a direct and selective synthesis of the useful nitriles by an aerobic oxidation reaction of primary amines using air as an advantageous oxidant under mild conditions.
AbstractList [Display omitted] A simple and readily available CuCl/DMEDA/TEMPO system-catalyzed aerobic oxidation of primary amines using air as an advantageous oxidant is developed for direct and selective synthesis of the useful nitriles under mild conditions. By screening the copper catalysts, ligands, and the reaction conditions, a simple CuCl/DMEDA/TEMPO catalyst system readily available from commercial sources is developed for a direct and selective synthesis of the useful nitriles by an aerobic oxidation reaction of primary amines using air as an advantageous oxidant under mild conditions.
By screening the copper catalysts, ligands, and the reaction conditions, a simple CuCl/DMEDA/TEMPO catalyst system readily available from commercial sources is developed for a direct and selective synthesis of the useful nitriles by an aerobic oxidation reaction of primary amines using air as an advantageous oxidant under mild conditions. (C) 2017 Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences. Published by Elsevier B.V. All rights reserved.
By screening the copper catalysts,ligands,and the reaction conditions,a simple CuCl/DMEDA/TEMPO catalyst system readily available from commercial sources is developed for a direct and selective synthesis of the useful nitriles by an aerobic oxidation reaction of primary amines using air as an advantageous oxidant under mild conditions.
Author Xian-Tao Ma Hao Xu Ying-Lin Xiao Chen-Liang Su Jian-Ping Liu Qing Xu
AuthorAffiliation SZU-NUS Collaborative Innovation Center for Optoelectronic Science ＆ Technology, Key Laboratory of Optoelectronic Devices and Systems of Ministry ofEducation and Guangdong Province, College of Optoelectronic Engineering, Shenzhen University, Shenzhen 518060, China College of Chemistry and Materials Engineering Department, Wenzhou University, Wenzhou 325035, China
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Cites_doi 10.1039/jr9640001097
10.1021/ja409223a
10.1016/j.tetlet.2015.12.082
10.1021/ja983635v
10.1021/om701148t
10.1002/adsc.201200574
10.1002/anie.200605004
10.1039/c3gc42310g
10.1002/anie.200353461
10.1002/1521-3773(20020816)41:16<2983::AID-ANIE2983>3.0.CO;2-X
10.1016/j.cclet.2014.04.024
10.1002/jctb.1795
10.1055/s-1977-24333
10.1039/C5CY00011D
10.1016/j.tetlet.2013.03.098
10.1039/c1cc14242a
10.1039/c3gc36513a
10.1021/ar0000354
10.6023/cjoc201208016
10.1002/chem.201301596
10.1039/c4cc01389a
10.1021/cr00080a006
10.1021/ol4010118
10.1002/chem.201501823
10.1016/S0920-5861(98)00418-0
10.1002/cssc.201402613
10.1002/adsc.201300453
10.1021/cs400360e
10.1016/S0040-4039(97)10575-5
10.1016/j.cclet.2015.01.009
10.1002/anie.201403110
10.1021/cs501186n
10.1039/C6GC01565D
10.1021/jacs.5b13307
10.1007/s10562-016-1818-2
10.1021/jo048240a
10.1021/ja056740v
10.1039/b919346b
10.1039/c6gc01565d
10.1039/c5cy00011d
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Issue 6
Keywords Nitriles
Amines
Air
Copper catalysis
Aerobic oxidation
ROOM-TEMPERATURE
CONVERSION
IMINES
HYDRATION
ALCOHOLS
EFFICIENT CATALYST
DEHYDROGENATION
ARYL HALIDES
METAL
AMIDES
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Notes Aerobic oxidation Air Amines Copper catalysis Nitriles
11-2710/O6
By screening the copper catalysts,ligands,and the reaction conditions,a simple CuCl/DMEDA/TEMPO catalyst system readily available from commercial sources is developed for a direct and selective synthesis of the useful nitriles by an aerobic oxidation reaction of primary amines using air as an advantageous oxidant under mild conditions.
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References Bacon, Hill (bib0045) 1964
Benz, Muntwyler, Wohlgemuth (bib0050) 2007; 82
Huang, Tian, Lin (bib0200) 2013; 54
Grasselli (bib0060) 1999; 49
Bagherzade, Zali, Shokrolahi (bib0095) 2015; 26
Mahadevan, DuBois, Hedman, Hodgson, Stack (bib0140) 1999; 121
Ma, Su, Xu (bib0175) 2016; 374
Ovoshchnikov, Donoeva, Golovko (bib0130) 2015; 5
Ishihara, Furuya, Yamamoto (bib0070) 2002; 41
Zhu, Li, Shen (bib0075) 2016; 21
Kim, Stahl (bib0155) 2013; 3
Miller, Manson (bib0015) 2001; 34
Bernskoetter, Brookhart (bib0100) 2008; 27
Liu, Wang, Ma (bib0205) 2016; 146
Ellis, Alexander (bib0055) 1987; 87
Wang, Lu, Cao, Gu (bib0150) 2014; 50
Jnaneshwara, Deshpande, Lalithambika, Ravindranathan, Bedekar (bib0030) 1998; 39
Corker, Mentzel, Mielby, Riisager, Fehrmann (bib0120) 2013; 15
Varyani, Khatri, Jain (bib0160) 2016; 57
Jiang, Jin, Tian (bib0185) 2011; 47
Yamaguchi, Matsushita, Mizuno (bib0020) 2004; 43
Zhang, Tian, Xu, Yu, Xu (bib0195) 2013; 15
Damodara, Arundhathi, Likhar (bib0110) 2014; 356
Chen, Dai, Chen (bib0035) 2014; 16
Pollak, Romeder, Hagedorn (bib0005) 2012
Ye, Zhang, Zha, Wang (bib0170) 2014; 25
Tseng, Rizzi, Szymczak (bib0105) 2013; 135
Ryland, Stahl (bib0085) 2014; 53
Hammond, Schuemperli, Hermans (bib0135) 2013; 19
Mirica, Rudd, Vance (bib0145) 2006; 128
Jagadeesh, Junge, Beller (bib0165) 2015; 8
Li, Chen, Liu, Wan, Xu (bib0040) 2016; 18
Moorthy, Singhal (bib0025) 2005; 70
Yamaguchi, Fujiwara, Ogasawara (bib0065) 2007; 46
Zhang, Wang, Wang (bib0090) 2009; 11
Pavel, Goodrich, Cristian (bib0125) 2015; 5
Xu, Li (bib0180) 2013; 33
Mondal, Acharyya, Howlader, Mukherjee (bib0080) 2016; 138
Tian, Yu, Li, Wang, Xu (bib0190) 2012; 354
Fatiadi (bib0010) 1983
Kametani, Takahashi, Ohsawa, Ihara (bib0115) 1977
Moorthy (10.1016/j.cclet.2017.01.017_bib0025) 2005; 70
Ovoshchnikov (10.1016/j.cclet.2017.01.017_bib0130) 2015; 5
Bagherzade (10.1016/j.cclet.2017.01.017_bib0095) 2015; 26
Tian (10.1016/j.cclet.2017.01.017_bib0190) 2012; 354
Xu (10.1016/j.cclet.2017.01.017_bib0180) 2013; 33
Yamaguchi (10.1016/j.cclet.2017.01.017_bib0065) 2007; 46
Varyani (10.1016/j.cclet.2017.01.017_bib0160) 2016; 57
Huang (10.1016/j.cclet.2017.01.017_bib0200) 2013; 54
Ye (10.1016/j.cclet.2017.01.017_bib0170) 2014; 25
Kametani (10.1016/j.cclet.2017.01.017_bib0115) 1977
Chen (10.1016/j.cclet.2017.01.017_bib0035) 2014; 16
Benz (10.1016/j.cclet.2017.01.017_bib0050) 2007; 82
Ishihara (10.1016/j.cclet.2017.01.017_bib0070) 2002; 41
Bernskoetter (10.1016/j.cclet.2017.01.017_bib0100) 2008; 27
Tseng (10.1016/j.cclet.2017.01.017_bib0105) 2013; 135
Liu (10.1016/j.cclet.2017.01.017_bib0205) 2016; 146
Jagadeesh (10.1016/j.cclet.2017.01.017_bib0165) 2015; 8
Zhu (10.1016/j.cclet.2017.01.017_bib0075) 2016; 21
Wang (10.1016/j.cclet.2017.01.017_bib0150) 2014; 50
Fatiadi (10.1016/j.cclet.2017.01.017_bib0010) 1983
Mondal (10.1016/j.cclet.2017.01.017_bib0080) 2016; 138
Grasselli (10.1016/j.cclet.2017.01.017_bib0060) 1999; 49
Miller (10.1016/j.cclet.2017.01.017_bib0015) 2001; 34
Yamaguchi (10.1016/j.cclet.2017.01.017_bib0020) 2004; 43
Bacon (10.1016/j.cclet.2017.01.017_bib0045) 1964
Jnaneshwara (10.1016/j.cclet.2017.01.017_bib0030) 1998; 39
Li (10.1016/j.cclet.2017.01.017_bib0040) 2016; 18
Hammond (10.1016/j.cclet.2017.01.017_bib0135) 2013; 19
Ellis (10.1016/j.cclet.2017.01.017_bib0055) 1987; 87
Damodara (10.1016/j.cclet.2017.01.017_bib0110) 2014; 356
Kim (10.1016/j.cclet.2017.01.017_bib0155) 2013; 3
Corker (10.1016/j.cclet.2017.01.017_bib0120) 2013; 15
Pavel (10.1016/j.cclet.2017.01.017_bib0125) 2015; 5
Ma (10.1016/j.cclet.2017.01.017_bib0175) 2016; 374
Mahadevan (10.1016/j.cclet.2017.01.017_bib0140) 1999; 121
Mirica (10.1016/j.cclet.2017.01.017_bib0145) 2006; 128
Jiang (10.1016/j.cclet.2017.01.017_bib0185) 2011; 47
Pollak (10.1016/j.cclet.2017.01.017_bib0005) 2012
Zhang (10.1016/j.cclet.2017.01.017_bib0195) 2013; 15
Ryland (10.1016/j.cclet.2017.01.017_bib0085) 2014; 53
Zhang (10.1016/j.cclet.2017.01.017_bib0090) 2009; 11
Zhang, JT (WOS:000272382200010) 2009; 11
Damodara, D (WOS:000331059200012) 2014; 356
Wang, JQ (WOS:000335460800027) 2014; 50
Grasselli, RK (WOS:000078946100019) 1999; 49
Moorthy, JN (WOS:000227246800058) 2005; 70
Kim, J (WOS:000321606100027) 2013; 3
Corker, EC (WOS:000316691100010) 2013; 15
Fatiadi, A.J. (000404696800037.9) 1983
Xu, Q (WOS:000315605400002) 2013; 33
Bernskoetter, WH (WOS:000255373400012) 2008; 27
Mondal, B (WOS:000370215400035) 2016; 138
Ovoshchnikov, DS (WOS:000347513400006) 2015; 5
Ma, X. (000404696800037.21) 2016; 374
Pavel, OD (WOS:000353641800017) 2015; 5
BACON, RGR (WOS:A19644238B00005) 1964
Ye, JQ (WOS:000345880300002) 2014; 25
Ishihara, K (WOS:000177597700020) 2002; 41
Liu, JP (WOS:000385196700033) 2016; 146
Yamaguchi, K (WOS:000220389600026) 2004; 43
Zhang, EL (WOS:000320298900035) 2013; 15
Tian, HW (WOS:000309907300012) 2012; 354
Li, Y (WOS:000383999300006) 2016; 18
Jiang, L (WOS:000295004300098) 2011; 47
Jagadeesh, RV (WOS:000347541700011) 2015; 8
Chen, HN (WOS:000333331200049) 2014; 16
KAMETANI, T (WOS:A1977DC37700006) 1977
Zhu, YM (WOS:000360829600016) 2015; 21
Pollak, G. (000404696800037.29) 2012
Varyani, M (WOS:000369550100002) 2016; 57
Huang, B (WOS:000318664900028) 2013; 54
ELLIS, GP (WOS:A1987J522800006) 1987; 87
Mahadevan, V (WOS:000081006000031) 1999; 121
Tseng, KNT (WOS:000326774300028) 2013; 135
Yamaguchi, K (WOS:000246832900024) 2007; 46
Miller, JS (WOS:000170173900005) 2001; 34
Hammond, C (WOS:000324579600039) 2013; 19
Jnaneshwara, GK (WOS:000071241100033) 1998; 39
Ryland, BL (WOS:000340526400002) 2014; 53
Bagherzade, G (WOS:000356116300024) 2015; 26
Mirica, LM (WOS:000235787200041) 2006; 128
Benz, P (WOS:000251379400007) 2007; 82
References_xml – volume: 135
  start-page: 16352
  year: 2013
  end-page: 16355
  ident: bib0105
  article-title: Oxidant-free conversion of primary amines to nitriles
  publication-title: J. Am. Chem. Soc.
– volume: 47
  start-page: 10833
  year: 2011
  end-page: 10835
  ident: bib0185
  article-title: Direct and mild palladium-catalyzed aerobic oxidative synthesis of imines from alcohols and amines under ambient conditions
  publication-title: Chem. Commun.
– volume: 15
  start-page: 2704
  year: 2013
  end-page: 2707
  ident: bib0195
  article-title: Iron-catalyzed direct synthesis of imines from amines or alcohols and amines via aerobic oxidative reactions under air
  publication-title: Org. Lett.
– volume: 356
  start-page: 189
  year: 2014
  end-page: 198
  ident: bib0110
  article-title: Copper nanoparticles from copper aluminum hydrotalcite: an efficient catalyst for acceptor-and oxidant-free dehydrogenation of amines and alcohols
  publication-title: Adv. Synth. Catal.
– volume: 50
  start-page: 5637
  year: 2014
  end-page: 5640
  ident: bib0150
  article-title: Common metal of copper (0) as an efficient catalyst for preparation of nitriles and imines by controlling additives
  publication-title: Chem. Commun.
– volume: 49
  start-page: 141
  year: 1999
  end-page: 153
  ident: bib0060
  article-title: Advances and future trends in selective oxidation and ammoxidation catalysis
  publication-title: Catal. Today
– volume: 138
  start-page: 1709
  year: 2016
  end-page: 1716
  ident: bib0080
  article-title: Molecular cage impregnated palladium nanoparticles: efficient additive-free heterogeneous catalysts for cyanation of aryl halides
  publication-title: J. Am. Chem. Soc.
– volume: 54
  start-page: 2861
  year: 2013
  end-page: 2864
  ident: bib0200
  article-title: Cu (I)/TEMPO-catalyzed aerobic oxidative synthesis of imines directly from primary and secondary amines under ambient and neat conditions
  publication-title: Tetrahedron Lett.
– volume: 18
  start-page: 4865
  year: 2016
  end-page: 4870
  ident: bib0040
  article-title: Clean synthesis of primary to tertiary carboxamides by CsOH-catalyzed aminolysis of nitriles in water
  publication-title: Green Chem.
– volume: 34
  start-page: 563
  year: 2001
  end-page: 570
  ident: bib0015
  article-title: Designer magnets containing cyanides and nitriles
  publication-title: Acc. Chem. Res.
– year: 2012
  ident: bib0005
  article-title: Ullmann’s Encyclopedia of Industrial Chemistry
– volume: 121
  start-page: 5583
  year: 1999
  end-page: 5584
  ident: bib0140
  article-title: Exogenous substrate reactivity with a [Cu(III)
  publication-title: J. Am. Chem. Soc.
– start-page: 1057
  year: 1983
  end-page: 1303
  ident: bib0010
  article-title: Preparation and Synthetic Applications of Cyano Compounds
  publication-title: Triple-Bonded Functional Groups
– volume: 33
  start-page: 18
  year: 2013
  end-page: 35
  ident: bib0180
  article-title: Recent advances of transition metal-catalyzed aerobic dehydrative reactions of alcohols and amines and related researches
  publication-title: Chin. J. Org. Chem.
– volume: 39
  start-page: 459
  year: 1998
  end-page: 462
  ident: bib0030
  article-title: Natural Kaolinitic clay catalyzed conversion of nitriles to 2-oxazolines
  publication-title: Tetrahedron Lett.
– volume: 25
  start-page: 1112
  year: 2014
  end-page: 1114
  ident: bib0170
  article-title: A green and efficient access to aryl nitriles via an electrochemical anodic oxidation
  publication-title: Chin. Chem. Lett.
– volume: 16
  start-page: 2136
  year: 2014
  end-page: 2141
  ident: bib0035
  article-title: Efficient and selective nitrile hydration reaction in water catalyzed by unexpected dimethylsulfinyl anion generated
  publication-title: Green Chem.
– volume: 87
  start-page: 779
  year: 1987
  end-page: 794
  ident: bib0055
  article-title: Cyanation of aromatic halides
  publication-title: Chem. Rev.
– volume: 11
  start-page: 1973
  year: 2009
  end-page: 1978
  ident: bib0090
  article-title: A metal-free catalytic system for the oxidation of benzylic methylenes and primary amines under solvent-free conditions
  publication-title: Green Chem.
– volume: 82
  start-page: 1087
  year: 2007
  end-page: 1098
  ident: bib0050
  article-title: Chemoenzymatic synthesis of chiral carboxylic acids via nitriles
  publication-title: J. Chem. Technol. Biotechnol.
– volume: 41
  start-page: 2983
  year: 2002
  end-page: 2986
  ident: bib0070
  article-title: Rhenium (VII) oxo complexes as extremely active catalysts in the dehydration of primary amides and aldoximes to nitriles
  publication-title: Angew. Chem. Int. Ed.
– volume: 21
  start-page: 13246
  year: 2016
  end-page: 13252
  ident: bib0075
  article-title: Cu-catalyzed cyanation of arylboronic acids with acetonitrile: a dual role of TEMPO
  publication-title: Chem. A Eur. J.
– volume: 5
  start-page: 2696
  year: 2015
  end-page: 2704
  ident: bib0125
  article-title: Direct oxidation of amines to nitriles in the presence of ruthenium-terpyridyl complex immobilized on ILs/SILP
  publication-title: Catal. Sci. Technol.
– volume: 53
  start-page: 8824
  year: 2014
  end-page: 8838
  ident: bib0085
  article-title: Practical aerobic oxidations of alcohols and amines with homogeneous copper/TEMPO and related catalyst systems
  publication-title: Angew. Chem. Int. Ed.
– volume: 5
  start-page: 34
  year: 2015
  end-page: 38
  ident: bib0130
  article-title: Visible-light-driven aerobic oxidation of amines to nitriles over hydrous ruthenium oxide supported on TiO
  publication-title: ACS Catal.
– volume: 3
  start-page: 1652
  year: 2013
  end-page: 1656
  ident: bib0155
  article-title: Cu/Nitroxyl-catalyzed aerobic oxidation of primary amines into nitriles at room temperature
  publication-title: ACS Catal.
– volume: 46
  start-page: 3922
  year: 2007
  end-page: 3925
  ident: bib0065
  article-title: A tungsten–tin mixed hydroxide as an efficient heterogeneous catalyst for dehydration of aldoximes to nitriles
  publication-title: Angew. Chem. Int. Ed.
– start-page: 1097
  year: 1964
  end-page: 1107
  ident: bib0045
  article-title: Metal ions and complexes in organic reactions. Part I. Substitution reactions between aryl halides and cuprous salts in organic solvents
  publication-title: J. Chem. Soc.
– volume: 8
  start-page: 92
  year: 2015
  end-page: 96
  ident: bib0165
  article-title: Nanorust-catalyzed benign oxidation of amines for selective synthesis of nitriles
  publication-title: ChemSusChem
– volume: 354
  start-page: 2671
  year: 2012
  end-page: 2677
  ident: bib0190
  article-title: General, green, and scalable synthesis of imines from alcohols and amines by a mild and efficient copper-catalyzed aerobic oxidative reaction in open air at room temperature
  publication-title: Adv. Synth. Catal.
– volume: 146
  start-page: 2139
  year: 2016
  end-page: 2148
  ident: bib0205
  article-title: Simple synthesis of benzazoles by substrate-promoted CuI-catalyzed aerobic oxidative cyclocondensation of o-thio/amino/hydroxyanilines and amines under air
  publication-title: Catal. Lett.
– volume: 57
  start-page: 723
  year: 2016
  end-page: 727
  ident: bib0160
  article-title: Amino acid derived ionic liquid supported iron schiff base catalyzed greener approach for the aerobic oxidation of amines to nitriles
  publication-title: Tetrahedron Lett.
– volume: 43
  start-page: 1576
  year: 2004
  end-page: 1580
  ident: bib0020
  article-title: Efficient hydration of nitriles to amides in water, catalyzed by ruthenium hydroxide supported on alumina
  publication-title: Angew. Chem. Int. Ed.
– volume: 15
  start-page: 928
  year: 2013
  end-page: 933
  ident: bib0120
  article-title: An alternative pathway for production of acetonitrile: ruthenium catalysed aerobic dehydrogenation of ethylamine
  publication-title: Green Chem.
– volume: 374
  start-page: 1
  year: 2016
  end-page: 74
  ident: bib0175
  article-title: N-Alkylation by hydrogen autotransfer reactions in hydrogen transfer reactions: reductions and beyond (Eds. G. Guillena, D. J. Ramón)
  publication-title: Top. Curr. Chem.
– volume: 27
  start-page: 2036
  year: 2008
  end-page: 2045
  ident: bib0100
  article-title: Kinetics and mechanism of iridium-catalyzed dehydrogenation of primary amines to nitriles
  publication-title: Organometallics
– volume: 19
  start-page: 13193
  year: 2013
  end-page: 13198
  ident: bib0135
  article-title: Insights into the oxidative dehydrogenation of amines with nanoparticulate iridium oxide
  publication-title: Chem. Eur. J.
– volume: 70
  start-page: 1926
  year: 2005
  end-page: 1929
  ident: bib0025
  article-title: Facile and highly selective conversion of nitriles to amides
  publication-title: J. Org. Chem.
– start-page: 245
  year: 1977
  ident: bib0115
  article-title: Oxidation of amines to nitriles or aldehydes using copper (I) chloride
  publication-title: Synthesis
– volume: 26
  start-page: 603
  year: 2015
  end-page: 606
  ident: bib0095
  article-title: Preparation of aromatic nitriles via direct oxidative conversion of benzyl alcohols, aldehydes and amines with pentylpyridinium tribromide in aqueous NH
  publication-title: Chin. Chem. Lett.
– volume: 128
  start-page: 2654
  year: 2006
  end-page: 2665
  ident: bib0145
  article-title: Peroxodicopper (II) complex with a secondary diamine ligand: a functional model of tyrosinase
  publication-title: J. Am. Chem. Soc.
– start-page: 1097
  year: 1964
  ident: 10.1016/j.cclet.2017.01.017_bib0045
  article-title: Metal ions and complexes in organic reactions. Part I. Substitution reactions between aryl halides and cuprous salts in organic solvents
  publication-title: J. Chem. Soc.
  doi: 10.1039/jr9640001097
– volume: 135
  start-page: 16352
  year: 2013
  ident: 10.1016/j.cclet.2017.01.017_bib0105
  article-title: Oxidant-free conversion of primary amines to nitriles
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja409223a
– volume: 57
  start-page: 723
  year: 2016
  ident: 10.1016/j.cclet.2017.01.017_bib0160
  article-title: Amino acid derived ionic liquid supported iron schiff base catalyzed greener approach for the aerobic oxidation of amines to nitriles
  publication-title: Tetrahedron Lett.
  doi: 10.1016/j.tetlet.2015.12.082
– volume: 121
  start-page: 5583
  year: 1999
  ident: 10.1016/j.cclet.2017.01.017_bib0140
  article-title: Exogenous substrate reactivity with a [Cu(III)2O2]2+ core: structural implications
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja983635v
– volume: 27
  start-page: 2036
  year: 2008
  ident: 10.1016/j.cclet.2017.01.017_bib0100
  article-title: Kinetics and mechanism of iridium-catalyzed dehydrogenation of primary amines to nitriles
  publication-title: Organometallics
  doi: 10.1021/om701148t
– volume: 354
  start-page: 2671
  year: 2012
  ident: 10.1016/j.cclet.2017.01.017_bib0190
  article-title: General, green, and scalable synthesis of imines from alcohols and amines by a mild and efficient copper-catalyzed aerobic oxidative reaction in open air at room temperature
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.201200574
– volume: 46
  start-page: 3922
  year: 2007
  ident: 10.1016/j.cclet.2017.01.017_bib0065
  article-title: A tungsten–tin mixed hydroxide as an efficient heterogeneous catalyst for dehydration of aldoximes to nitriles
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.200605004
– volume: 16
  start-page: 2136
  year: 2014
  ident: 10.1016/j.cclet.2017.01.017_bib0035
  article-title: Efficient and selective nitrile hydration reaction in water catalyzed by unexpected dimethylsulfinyl anion generated in situ from CsOH and DMSO
  publication-title: Green Chem.
  doi: 10.1039/c3gc42310g
– volume: 43
  start-page: 1576
  year: 2004
  ident: 10.1016/j.cclet.2017.01.017_bib0020
  article-title: Efficient hydration of nitriles to amides in water, catalyzed by ruthenium hydroxide supported on alumina
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.200353461
– volume: 41
  start-page: 2983
  year: 2002
  ident: 10.1016/j.cclet.2017.01.017_bib0070
  article-title: Rhenium (VII) oxo complexes as extremely active catalysts in the dehydration of primary amides and aldoximes to nitriles
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/1521-3773(20020816)41:16<2983::AID-ANIE2983>3.0.CO;2-X
– volume: 25
  start-page: 1112
  year: 2014
  ident: 10.1016/j.cclet.2017.01.017_bib0170
  article-title: A green and efficient access to aryl nitriles via an electrochemical anodic oxidation
  publication-title: Chin. Chem. Lett.
  doi: 10.1016/j.cclet.2014.04.024
– volume: 82
  start-page: 1087
  year: 2007
  ident: 10.1016/j.cclet.2017.01.017_bib0050
  article-title: Chemoenzymatic synthesis of chiral carboxylic acids via nitriles
  publication-title: J. Chem. Technol. Biotechnol.
  doi: 10.1002/jctb.1795
– start-page: 245
  year: 1977
  ident: 10.1016/j.cclet.2017.01.017_bib0115
  article-title: Oxidation of amines to nitriles or aldehydes using copper (I) chloride
  publication-title: Synthesis
  doi: 10.1055/s-1977-24333
– volume: 374
  start-page: 1
  issue: 27
  year: 2016
  ident: 10.1016/j.cclet.2017.01.017_bib0175
  article-title: N-Alkylation by hydrogen autotransfer reactions in hydrogen transfer reactions: reductions and beyond (Eds. G. Guillena, D. J. Ramón)
  publication-title: Top. Curr. Chem.
– volume: 5
  start-page: 2696
  year: 2015
  ident: 10.1016/j.cclet.2017.01.017_bib0125
  article-title: Direct oxidation of amines to nitriles in the presence of ruthenium-terpyridyl complex immobilized on ILs/SILP
  publication-title: Catal. Sci. Technol.
  doi: 10.1039/C5CY00011D
– volume: 54
  start-page: 2861
  year: 2013
  ident: 10.1016/j.cclet.2017.01.017_bib0200
  article-title: Cu (I)/TEMPO-catalyzed aerobic oxidative synthesis of imines directly from primary and secondary amines under ambient and neat conditions
  publication-title: Tetrahedron Lett.
  doi: 10.1016/j.tetlet.2013.03.098
– volume: 47
  start-page: 10833
  year: 2011
  ident: 10.1016/j.cclet.2017.01.017_bib0185
  article-title: Direct and mild palladium-catalyzed aerobic oxidative synthesis of imines from alcohols and amines under ambient conditions
  publication-title: Chem. Commun.
  doi: 10.1039/c1cc14242a
– year: 2012
  ident: 10.1016/j.cclet.2017.01.017_bib0005
– volume: 15
  start-page: 928
  year: 2013
  ident: 10.1016/j.cclet.2017.01.017_bib0120
  article-title: An alternative pathway for production of acetonitrile: ruthenium catalysed aerobic dehydrogenation of ethylamine
  publication-title: Green Chem.
  doi: 10.1039/c3gc36513a
– start-page: 1057
  year: 1983
  ident: 10.1016/j.cclet.2017.01.017_bib0010
  article-title: Preparation and Synthetic Applications of Cyano Compounds
– volume: 34
  start-page: 563
  year: 2001
  ident: 10.1016/j.cclet.2017.01.017_bib0015
  article-title: Designer magnets containing cyanides and nitriles
  publication-title: Acc. Chem. Res.
  doi: 10.1021/ar0000354
– volume: 33
  start-page: 18
  year: 2013
  ident: 10.1016/j.cclet.2017.01.017_bib0180
  article-title: Recent advances of transition metal-catalyzed aerobic dehydrative reactions of alcohols and amines and related researches
  publication-title: Chin. J. Org. Chem.
  doi: 10.6023/cjoc201208016
– volume: 19
  start-page: 13193
  year: 2013
  ident: 10.1016/j.cclet.2017.01.017_bib0135
  article-title: Insights into the oxidative dehydrogenation of amines with nanoparticulate iridium oxide
  publication-title: Chem. Eur. J.
  doi: 10.1002/chem.201301596
– volume: 50
  start-page: 5637
  year: 2014
  ident: 10.1016/j.cclet.2017.01.017_bib0150
  article-title: Common metal of copper (0) as an efficient catalyst for preparation of nitriles and imines by controlling additives
  publication-title: Chem. Commun.
  doi: 10.1039/c4cc01389a
– volume: 87
  start-page: 779
  year: 1987
  ident: 10.1016/j.cclet.2017.01.017_bib0055
  article-title: Cyanation of aromatic halides
  publication-title: Chem. Rev.
  doi: 10.1021/cr00080a006
– volume: 15
  start-page: 2704
  year: 2013
  ident: 10.1016/j.cclet.2017.01.017_bib0195
  article-title: Iron-catalyzed direct synthesis of imines from amines or alcohols and amines via aerobic oxidative reactions under air
  publication-title: Org. Lett.
  doi: 10.1021/ol4010118
– volume: 21
  start-page: 13246
  year: 2016
  ident: 10.1016/j.cclet.2017.01.017_bib0075
  article-title: Cu-catalyzed cyanation of arylboronic acids with acetonitrile: a dual role of TEMPO
  publication-title: Chem. A Eur. J.
  doi: 10.1002/chem.201501823
– volume: 49
  start-page: 141
  year: 1999
  ident: 10.1016/j.cclet.2017.01.017_bib0060
  article-title: Advances and future trends in selective oxidation and ammoxidation catalysis
  publication-title: Catal. Today
  doi: 10.1016/S0920-5861(98)00418-0
– volume: 8
  start-page: 92
  year: 2015
  ident: 10.1016/j.cclet.2017.01.017_bib0165
  article-title: Nanorust-catalyzed benign oxidation of amines for selective synthesis of nitriles
  publication-title: ChemSusChem
  doi: 10.1002/cssc.201402613
– volume: 356
  start-page: 189
  year: 2014
  ident: 10.1016/j.cclet.2017.01.017_bib0110
  article-title: Copper nanoparticles from copper aluminum hydrotalcite: an efficient catalyst for acceptor-and oxidant-free dehydrogenation of amines and alcohols
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.201300453
– volume: 3
  start-page: 1652
  year: 2013
  ident: 10.1016/j.cclet.2017.01.017_bib0155
  article-title: Cu/Nitroxyl-catalyzed aerobic oxidation of primary amines into nitriles at room temperature
  publication-title: ACS Catal.
  doi: 10.1021/cs400360e
– volume: 39
  start-page: 459
  year: 1998
  ident: 10.1016/j.cclet.2017.01.017_bib0030
  article-title: Natural Kaolinitic clay catalyzed conversion of nitriles to 2-oxazolines
  publication-title: Tetrahedron Lett.
  doi: 10.1016/S0040-4039(97)10575-5
– volume: 26
  start-page: 603
  year: 2015
  ident: 10.1016/j.cclet.2017.01.017_bib0095
  article-title: Preparation of aromatic nitriles via direct oxidative conversion of benzyl alcohols, aldehydes and amines with pentylpyridinium tribromide in aqueous NH4OAc
  publication-title: Chin. Chem. Lett.
  doi: 10.1016/j.cclet.2015.01.009
– volume: 53
  start-page: 8824
  year: 2014
  ident: 10.1016/j.cclet.2017.01.017_bib0085
  article-title: Practical aerobic oxidations of alcohols and amines with homogeneous copper/TEMPO and related catalyst systems
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.201403110
– volume: 5
  start-page: 34
  year: 2015
  ident: 10.1016/j.cclet.2017.01.017_bib0130
  article-title: Visible-light-driven aerobic oxidation of amines to nitriles over hydrous ruthenium oxide supported on TiO2
  publication-title: ACS Catal.
  doi: 10.1021/cs501186n
– volume: 18
  start-page: 4865
  year: 2016
  ident: 10.1016/j.cclet.2017.01.017_bib0040
  article-title: Clean synthesis of primary to tertiary carboxamides by CsOH-catalyzed aminolysis of nitriles in water
  publication-title: Green Chem.
  doi: 10.1039/C6GC01565D
– volume: 138
  start-page: 1709
  year: 2016
  ident: 10.1016/j.cclet.2017.01.017_bib0080
  article-title: Molecular cage impregnated palladium nanoparticles: efficient additive-free heterogeneous catalysts for cyanation of aryl halides
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.5b13307
– volume: 146
  start-page: 2139
  year: 2016
  ident: 10.1016/j.cclet.2017.01.017_bib0205
  article-title: Simple synthesis of benzazoles by substrate-promoted CuI-catalyzed aerobic oxidative cyclocondensation of o-thio/amino/hydroxyanilines and amines under air
  publication-title: Catal. Lett.
  doi: 10.1007/s10562-016-1818-2
– volume: 70
  start-page: 1926
  year: 2005
  ident: 10.1016/j.cclet.2017.01.017_bib0025
  article-title: Facile and highly selective conversion of nitriles to amides via indirect acid-catalyzed hydration using TFA or AcOH-H2SO4
  publication-title: J. Org. Chem.
  doi: 10.1021/jo048240a
– volume: 128
  start-page: 2654
  year: 2006
  ident: 10.1016/j.cclet.2017.01.017_bib0145
  article-title: μ-η2: η2-Peroxodicopper (II) complex with a secondary diamine ligand: a functional model of tyrosinase
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja056740v
– volume: 11
  start-page: 1973
  year: 2009
  ident: 10.1016/j.cclet.2017.01.017_bib0090
  article-title: A metal-free catalytic system for the oxidation of benzylic methylenes and primary amines under solvent-free conditions
  publication-title: Green Chem.
  doi: 10.1039/b919346b
– volume: 15
  start-page: 2704
  year: 2013
  ident: WOS:000320298900035
  article-title: Iron-Catalyzed Direct Synthesis of Imines from Amines or Alcohols and Amines via Aerobic Oxidative Reactions under Air
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol4010118
– volume: 53
  start-page: 8824
  year: 2014
  ident: WOS:000340526400002
  article-title: Practical Aerobic Oxidations of Alcohols and Amines with Homogeneous Copper/TEMPO and Related Catalyst Systems
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201403110
– volume: 128
  start-page: 2654
  year: 2006
  ident: WOS:000235787200041
  article-title: mu-eta(2):eta(2)-Peroxodicopper(II) complex with a secondary diamine ligand: A functional model of tyrosinase
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja056740v
– volume: 18
  start-page: 4865
  year: 2016
  ident: WOS:000383999300006
  article-title: Clean synthesis of primary to tertiary carboxamides by CsOH-catalyzed aminolysis of nitriles in water
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c6gc01565d
– volume: 15
  start-page: 928
  year: 2013
  ident: WOS:000316691100010
  article-title: An alternative pathway for production of acetonitrile: ruthenium catalysed aerobic dehydrogenation of ethylamine
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c3gc36513a
– volume: 82
  start-page: 1087
  year: 2007
  ident: WOS:000251379400007
  article-title: Chemoenzymatic synthesis of chiral carboxylic acids via nitriles
  publication-title: JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY
  doi: 10.1002/jctb.1795
– volume: 34
  start-page: 563
  year: 2001
  ident: WOS:000170173900005
  article-title: Designer magnets containing cyanides and nitriles
  publication-title: ACCOUNTS OF CHEMICAL RESEARCH
  doi: 10.1021/ar0000354
– volume: 26
  start-page: 603
  year: 2015
  ident: WOS:000356116300024
  article-title: Preparation of aromatic nitriles via direct oxidative conversion of benzyl alcohols, aldehydes and amines with pentylpyridinium tribromide in aqueous NH4OAc
  publication-title: CHINESE CHEMICAL LETTERS
  doi: 10.1016/j.cclet.2015.01.009
– volume: 356
  start-page: 189
  year: 2014
  ident: WOS:000331059200012
  article-title: Copper Nanoparticles from Copper Aluminum Hydrotalcite: An Efficient Catalyst for Acceptor- and Oxidant-Free Dehydrogenation of Amines and Alcohols
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201300453
– start-page: 1057
  year: 1983
  ident: 000404696800037.9
  article-title: Preparation and Synthetic Applications of Cyano Compounds
  publication-title: Triple-Bonded Functional Groups
– start-page: 1097
  year: 1964
  ident: WOS:A19644238B00005
  article-title: METAL IONS + COMPLEXES IN ORGANIC REACTIONS .I. SUBSTITUTION REACTIONS BETWEEN ARYL HALIDES + CUPROUS SALTS IN ORGANIC SOLVENTS
  publication-title: JOURNAL OF THE CHEMICAL SOCIETY
– volume: 27
  start-page: 2036
  year: 2008
  ident: WOS:000255373400012
  article-title: Kinetics and mechanism of iridium-catalyzed dehydrogenation of primary amines to nitriles
  publication-title: ORGANOMETALLICS
  doi: 10.1021/om701148t
– volume: 138
  start-page: 1709
  year: 2016
  ident: WOS:000370215400035
  article-title: Molecular Cage Impregnated Palladium Nanoparticles: Efficient, Additive-Free Heterogeneous Catalysts for Cyanation of Aryl Halides
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.5b13307
– volume: 87
  start-page: 779
  year: 1987
  ident: WOS:A1987J522800006
  article-title: CYANATION OF AROMATIC HALIDES
  publication-title: CHEMICAL REVIEWS
– volume: 70
  start-page: 1926
  year: 2005
  ident: WOS:000227246800058
  article-title: Facile and highly selective conversion of nitriles to amides via indirect acid-catalyzed hydration using TFA or AcOH-H2SO4
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/jo048240a
– volume: 121
  start-page: 5583
  year: 1999
  ident: WOS:000081006000031
  article-title: Exogenous substrate reactivity with a [Cu(III)(2)O-2](2+) core: Structural implications
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
– year: 2012
  ident: 000404696800037.29
  publication-title: Ullmann's Encyclopedia of Industrial Chemistry
– volume: 374
  start-page: 1
  year: 2016
  ident: 000404696800037.21
  article-title: N-Alkylation by hydrogen autotransfer reactions in hydrogen transfer reactions: reductions and beyond
  publication-title: Top. Curr. Chem
– volume: 47
  start-page: 10833
  year: 2011
  ident: WOS:000295004300098
  article-title: Direct and mild palladium-catalyzed aerobic oxidative synthesis of imines from alcohols and amines under ambient conditions
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c1cc14242a
– volume: 41
  start-page: 2983
  year: 2002
  ident: WOS:000177597700020
  article-title: Rheniumn(VII) oxo complexes as extremely active catalysts in the dehydration of primary amides and aldoximes to nitriles
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
– volume: 5
  start-page: 2696
  year: 2015
  ident: WOS:000353641800017
  article-title: Direct oxidation of amines to nitriles in the presence of ruthenium-terpyridyl complex immobilized on ILs/SILP
  publication-title: CATALYSIS SCIENCE & TECHNOLOGY
  doi: 10.1039/c5cy00011d
– volume: 50
  start-page: 5637
  year: 2014
  ident: WOS:000335460800027
  article-title: Common metal of copper(0) as an efficient catalyst for preparation of nitriles and imines by controlling additives
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c4cc01389a
– volume: 5
  start-page: 34
  year: 2015
  ident: WOS:000347513400006
  article-title: Visible-Light-Driven Aerobic Oxidation of Amines to Nitriles over Hydrous Ruthenium Oxide Supported on TiO2
  publication-title: ACS CATALYSIS
  doi: 10.1021/cs501186n
– volume: 43
  start-page: 1576
  year: 2004
  ident: WOS:000220389600026
  article-title: Efficient hydration of nitriles to amides in water, catalyzed by ruthenium hydroxide supported on alumina
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.200353461
– volume: 39
  start-page: 459
  year: 1998
  ident: WOS:000071241100033
  article-title: Natural kaolinitic clay catalyzed conversion of nitriles to 2-oxazolines
  publication-title: TETRAHEDRON LETTERS
– volume: 11
  start-page: 1973
  year: 2009
  ident: WOS:000272382200010
  article-title: A metal-free catalytic system for the oxidation of benzylic methylenes and primary amines under solvent-free conditions
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/b919346b
– volume: 57
  start-page: 723
  year: 2016
  ident: WOS:000369550100002
  article-title: Amino acid derived ionic liquid supported iron Schiff base catalyzed greener approach for the aerobic oxidation of amines to nitriles
  publication-title: TETRAHEDRON LETTERS
  doi: 10.1016/j.tetlet.2015.12.082
– volume: 46
  start-page: 3922
  year: 2007
  ident: WOS:000246832900024
  article-title: A tungsten-tin mixed hydroxide as an efficient heterogeneous catalyst for dehydration of aldoximes to nitriles
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.200605004
– volume: 21
  start-page: 13246
  year: 2015
  ident: WOS:000360829600016
  article-title: Cu-Catalyzed Cyanation of Arylboronic Acids with Acetonitrile: A Dual Role of TEMPO
  publication-title: CHEMISTRY-A EUROPEAN JOURNAL
  doi: 10.1002/chem.201501823
– volume: 33
  start-page: 18
  year: 2013
  ident: WOS:000315605400002
  article-title: Recent Advances of Transition Metal-Catalyzed Aerobic Dehydrative Reactions of Alcohols and Amines and Related Researches
  publication-title: CHINESE JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.6023/cjoc201208016
– volume: 54
  start-page: 2861
  year: 2013
  ident: WOS:000318664900028
  article-title: Cu(I)/TEMPO-catalyzed aerobic oxidative synthesis of imines directly from primary and secondary amines under ambient and neat conditions
  publication-title: TETRAHEDRON LETTERS
  doi: 10.1016/j.tetlet.2013.03.098
– volume: 19
  start-page: 13193
  year: 2013
  ident: WOS:000324579600039
  article-title: Insights into the Oxidative Dehydrogenation of Amines with Nanoparticulate Iridium Oxide
  publication-title: CHEMISTRY-A EUROPEAN JOURNAL
  doi: 10.1002/chem.201301596
– volume: 8
  start-page: 92
  year: 2015
  ident: WOS:000347541700011
  article-title: "Nanorust"-catalyzed Benign Oxidation of Amines for Selective Synthesis of Nitriles
  publication-title: CHEMSUSCHEM
  doi: 10.1002/cssc.201402613
– volume: 49
  start-page: 141
  year: 1999
  ident: WOS:000078946100019
  article-title: Advances and future trends in selective oxidation and ammoxidation catalysis
  publication-title: CATALYSIS TODAY
– volume: 3
  start-page: 1652
  year: 2013
  ident: WOS:000321606100027
  article-title: Cu/Nitroxyl-Catalyzed Aerobic Oxidation of Primary Amines into Nitriles at Room Temperature
  publication-title: ACS CATALYSIS
  doi: 10.1021/cs400360e
– volume: 25
  start-page: 1112
  year: 2014
  ident: WOS:000345880300002
  article-title: A green and efficient access to aryl nitriles via an electrochemical anodic oxidation
  publication-title: CHINESE CHEMICAL LETTERS
  doi: 10.1016/j.cclet.2014.04.024
– volume: 135
  start-page: 16352
  year: 2013
  ident: WOS:000326774300028
  article-title: Oxidant-Free Conversion of Primary Amines to Nitriles
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja409223a
– volume: 16
  start-page: 2136
  year: 2014
  ident: WOS:000333331200049
  article-title: Efficient and selective nitrile hydration reactions in water catalyzed by an unexpected dimethylsulfinyl anion generated in situ from CsOH and DMSO
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c3gc42310g
– volume: 146
  start-page: 2139
  year: 2016
  ident: WOS:000385196700033
  article-title: Simple Synthesis of Benzazoles by Substrate-Promoted CuI-Catalyzed Aerobic Oxidative Cyclocondensation of o-Thio/Amino/Hydroxyanilines and Amines under Air
  publication-title: CATALYSIS LETTERS
  doi: 10.1007/s10562-016-1818-2
– volume: 354
  start-page: 2671
  year: 2012
  ident: WOS:000309907300012
  article-title: General, Green, and Scalable Synthesis of Imines from Alcohols and Amines by a Mild and Efficient Copper-Catalyzed Aerobic Oxidative Reaction in Open Air at Room Temperature
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201200574
– start-page: 245
  year: 1977
  ident: WOS:A1977DC37700006
  article-title: OXIDATION OF AMINES TO NITRILES OR ALDEPHYDES USING COPPER(I) CHLORIDE
  publication-title: SYNTHESIS-STUTTGART
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Snippet By screening the copper catalysts,ligands,and the reaction conditions,a simple CuCl/DMEDA/TEMPO catalyst system readily available from commercial sources is...
[Display omitted] A simple and readily available CuCl/DMEDA/TEMPO system-catalyzed aerobic oxidation of primary amines using air as an advantageous oxidant is...
By screening the copper catalysts, ligands, and the reaction conditions, a simple CuCl/DMEDA/TEMPO catalyst system readily available from commercial sources is...
Source Web of Science
SourceID webofscience
crossref
elsevier
chongqing
SourceType Enrichment Source
Index Database
Publisher
StartPage 1336
SubjectTerms Aerobic oxidation
Air
Amines
Chemistry
Chemistry, Multidisciplinary
Copper catalysis
Nitriles
Physical Sciences
Science & Technology
Title Direct synthesis of nitriles by Cu/DMEDA/TEMPO-catalyzed aerobic oxidation of primary amines with air
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https://dx.doi.org/10.1016/j.cclet.2017.01.017
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