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C. Yeung, V. Dong (2011)
Catalytic dehydrogenative cross-coupling: forming carbon-carbon bonds by oxidizing two carbon-hydrogen bonds.Chemical reviews, 111 3
Congde Huo, Cheng Wang, Chougu Sun, Xiaodong Jia, Xi‐Cun Wang, Wenju Chang, Mingxia Wu (2013)
Triarylaminium Salt-Initiated Aerobic Double Friedel–Crafts Reaction of Glycine Derivatives with IndolesAdvanced Synthesis & Catalysis, 355
O. Baslé, Chao‐Jun Li (2007)
Copper catalyzed oxidative alkylation of sp3 C–H bond adjacent to a nitrogen atom using molecular oxygen in waterGreen Chemistry, 9
M. Rueping, C. Vila, Rene Koenigs, Konstantin Poscharny, David Fabry (2011)
Dual catalysis: combining photoredox and Lewis base catalysis for direct Mannich reactions.Chemical communications, 47 8
Chao Liu, Hua Zhang, W. Shi, A. Lei (2011)
Bond formations between two nucleophiles: transition metal catalyzed oxidative cross-coupling reactions.Chemical reviews, 111 3
Simone Girard, Thomas Knauber, Chao-Jun Li (2014)
Dehydrierende Kreuzkupplungen von C sp 3‐H‐Bindungen: vielseitige Verfahren zur Bildung von C‐C‐BindungenAngewandte Chemie, 126
Gen Zhang, Yaohu Zhang, Rui Wang (2011)
Catalytic asymmetric activation of a C(sp³)-H bond adjacent to a nitrogen atom: a versatile approach to optically active α-alkyl α-amino acids and C1-alkylated tetrahydroisoquinoline derivatives.Angewandte Chemie, 50 44
Chandra Volla, P. Vogel (2009)
Chemoselective C-H bond activation: ligand and solvent free iron-catalyzed oxidative C-C cross-coupling of tertiary amines with terminal alkynes. Reaction scope and mechanism.Organic letters, 11 8
Xiaoliang Xu, Xiaonian Li (2009)
Copper/diethyl azodicarboxylate mediated regioselective alkynylation of unactivated aliphatic tertiary methylamine with terminal alkyne.Organic letters, 11 4
Tomoya Nobuta, N. Tada, Akitoshi Fujiya, Atsumasa Kariya, T. Miura, A. Itoh (2013)
Molecular iodine catalyzed cross-dehydrogenative coupling reaction between two sp3 C-H bonds using hydrogen peroxide.Organic letters, 15 3
J. Xie, Zhi-zhen Huang (2010)
Cross-dehydrogenative coupling reactions by transition-metal and aminocatalysis for the synthesis of amino acid derivatives.Angewandte Chemie, 49 52
Yongming Deng, Siddhartha Kumar, Hong Wang (2014)
Synergistic-cooperative combination of enamine catalysis with transition metal catalysis.Chemical communications, 50 33
Zhiping Li, Chao‐Jun Li (2005)
CuBr-catalyzed direct indolation of tetrahydroisoquinolines via cross-dehydrogenative coupling between sp3 C-H and sp2 C-H bonds.Journal of the American Chemical Society, 127 19
Zhu‐Jia Feng, Jun Xuan, X. Xia, W. Ding, W. Guo, Jia‐Rong Chen, You‐Quan Zou, Liang‐Qiu Lu, W. Xiao (2014)
Direct sp(3)C-H acroleination of N-aryl-tetrahydroisoquinolines by merging photoredox catalysis with nucleophilic catalysis.Organic & biomolecular chemistry, 12 13
Peng Liu, Zhiming Wang, Jue Lin, Xianming Hu (2012)
An Efficient Route to Quinolines and Other Compounds by Iron‐Catalysed Cross‐Dehydrogenative Coupling Reactions of Glycine DerivativesEuropean Journal of Organic Chemistry, 2012
Junichiro Yamaguchi, A. Yamaguchi, K. Itami (2012)
C-H bond functionalization: emerging synthetic tools for natural products and pharmaceuticals.Angewandte Chemie, 51 36
L. Chu, Xingang Zhang, F. Qing (2009)
CuBr-catalyzed oxidative difluoromethylation of tertiary amines with difluoroenol silyl ethers.Organic letters, 11 10
S. Murahashi, Naruyoshi Komiya, Hiroyuki Terai, T. Nakae (2003)
Aerobic ruthenium-catalyzed oxidative cyanation of tertiary amines with sodium cyanide.Journal of the American Chemical Society, 125 50
E. Boess, C. Schmitz, M. Klussmann (2012)
A comparative mechanistic study of Cu-catalyzed oxidative coupling reactions with N-phenyltetrahydroisoquinoline.Journal of the American Chemical Society, 134 11
Lehao Huang, Xunbin Zhang, Yuhong Zhang (2009)
CuBr-catalyzed reaction of N,N-dimethylanilines and silyl enol ethers: an alternative route to beta-arylamino ketones.Organic letters, 11 16
Chao‐Jun Li (2009)
Cross-dehydrogenative coupling (CDC): exploring C-C bond formations beyond functional group transformations.Accounts of chemical research, 42 2
M. Ratnikov, M. Doyle (2013)
Mechanistic investigation of oxidative Mannich reaction with tert-butyl hydroperoxide. The role of transition metal salt.Journal of the American Chemical Society, 135 4
C. Min, Abbas Sanchawala, D. Seidel (2014)
Dual C–H Functionalization of N-Aryl Amines: Synthesis of Polycyclic Amines via an Oxidative Povarov ApproachOrganic Letters, 16
S. Cho, Ji Kim, Jaesung Kwak, Sukbok Chang (2011)
Recent advances in the transition metal-catalyzed twofold oxidative C-H bond activation strategy for C-C and C-N bond formation.Chemical Society reviews, 40 10
Simon Girard, Thomas Knauber, Chao‐Jun Li (2014)
The cross-dehydrogenative coupling of C(sp3)-H bonds: a versatile strategy for C-C bond formations.Angewandte Chemie, 53 1
Shaoqun Zhu, M. Rueping (2012)
Merging visible-light photoredox and Lewis acid catalysis for the functionalization and arylation of glycine derivatives and peptides.Chemical communications, 48 98
O. Baslé, Chao‐Jun Li (2008)
Copper-catalyzed oxidative sp3 C-H bond arylation with aryl boronic acids.Organic letters, 10 17
Zhiping Li, Chao‐Jun Li (2004)
CuBr-catalyzed efficient alkynylation of sp3 C-H bonds adjacent to a nitrogen atom.Journal of the American Chemical Society, 126 38
Junichiro Yamaguchi, Atsushi Yamaguchi, Kenichiro Itami (2012)
Funktionalisierung von C‐H‐Bindungen: neue Synthesemethoden für Naturstoffe und PharmazeutikaAngewandte Chemie, 124
Arata Tanoue, Woo‐Jin Yoo, S. Kobayashi (2014)
Sulfuryl chloride as an efficient initiator for the metal-free aerobic cross-dehydrogenative coupling reaction of tertiary amines.Organic letters, 16 9
Will Gutekunst, P. Baran (2011)
C-H functionalization logic in total synthesis.Chemical Society reviews, 40 4
O. Baslé, Chao‐Jun Li (2009)
Copper-catalyzed aerobic phosphonation of sp3 C-H bonds.Chemical communications, 27
Chun Zhang, Conghui Tang, N. Jiao (2012)
Recent advances in copper-catalyzed dehydrogenative functionalization via a single electron transfer (SET) process.Chemical Society reviews, 41 9
D. Chen, S. Youn (2012)
Activation : A Complementary Tool in the Total Synthesis of Complex Natural Products
M. Hopkinson, Basudev Sahoo, Jun‐Long Li, F. Glorius (2014)
Dual catalysis sees the light: combining photoredox with organo-, acid, and transition-metal catalysis.Chemistry, 20 14
K. Alagiri, Pradeep Devadig, K. Prabhu (2012)
CDC reactions of N-aryl tetrahydroisoquinolines using catalytic amounts of DDQ: C-H activation under aerobic conditions.Chemistry, 18 17
A. Allen, D. MacMillan (2012)
Synergistic Catalysis: A Powerful Synthetic Strategy for New Reaction Development.Chemical science, 2012 3
Zhiping Li, Chao‐Jun Li (2005)
Highly efficient copper-catalyzed nitro-Mannich type reaction: cross-dehydrogenative-coupling between sp3 C-H bond and sp3 C-H bond.Journal of the American Chemical Society, 127 11
Xiaodong Jia, Yaxin Wang, Fangfang Peng, Congde Huo, Liangliang Yu, Jing Liu, Xi‐Cun Wang (2013)
Catalytic sp3 C-H oxidation of peptides and their analogues by radical cation salts: from glycine amides to quinolines.The Journal of organic chemistry, 78 18
S. Murahashi, Dazhi Zhang (2008)
Ruthenium catalyzed biomimetic oxidation in organic synthesis inspired by cytochrome P-450.Chemical Society reviews, 37 8
Qing-Yuan Meng, Qiang Liu, Jian-Ji Zhong, Huihui Zhang, Zhi‐Jun Li, Bin Chen, C. Tung, Lizhu Wu (2012)
Graphene-supported RuO2 nanoparticles for efficient aerobic cross-dehydrogenative coupling reaction in water.Organic letters, 14 23
Congde Huo, Cheng Wang, Mingxia Wu, Xiaodong Jia, Haisheng Xie, Yong Yuan (2014)
Copper(I) Chloride-Catalyzed Aerobic Oxidative Arylation of Glycine Ester and Amide DerivativesAdvanced Synthesis & Catalysis, 356
Arata Tanoue, Woo‐Jin Yoo, S. Kobayashi (2013)
Antimony/N-Hydroxyphthalimide as a Catalyst System for Cross-Dehydrogenative Coupling Reactions under Aerobic ConditionsAdvanced Synthesis & Catalysis, 355
Lehao Huang, T. Niu, Jun Wu, Yuhong Zhang (2011)
Copper-catalyzed oxidative cross-coupling of N,N-dimethylanilines with heteroarenes under molecular oxygen.The Journal of organic chemistry, 76 6
M. Rueping, Rene Koenigs, Konstantin Poscharny, David Fabry, Daniele Leonori, C. Vila (2012)
Dual catalysis: combination of photocatalytic aerobic oxidation and metal catalyzed alkynylation reactions--C-C bond formation using visible light.Chemistry, 18 17
M. Niu, Z. Yin, H. Fu, Yuyang Jiang, Yufen Zhao (2008)
Copper-catalyzed coupling of tertiary aliphatic amines with terminal alkynes to propargylamines via C-H activation.The Journal of organic chemistry, 73 10
O. Baslé, N. Borduas, P. Dubois, J. Chapuzet, T. Chan, J. Lessard, Chao‐Jun Li (2010)
Aerobic and electrochemical oxidative cross-dehydrogenative-coupling (CDC) reaction in an imidazolium-based ionic liquid.Chemistry, 16 27
Zhiping Li, Chao‐Jun Li (2005)
Highly Efficient CuBr-Catalyzed Cross-Dehydrogenative Coupling (CDC) between Tetrahydroisoquinolines and Activated Methylene CompoundsEuropean Journal of Organic Chemistry, 2005
Liang Zhao, Oliver Baslé, Chao‐Jun Li (2009)
Site-specific C-functionalization of free-(NH) peptides and glycine derivatives via direct C–H bond functionalizationProceedings of the National Academy of Sciences, 106
Xiaodong Jia, Yaxin Wang, Fangfang Peng, Congde Huo, Lian Yu, Jing Liu, Xi‐Cun Wang (2014)
Catalytic Oxidation of C(sp3) ? H Bonds Induced by a Radical Cation Salt: Construction of 1,4‐Dihydropyridines Using a Fragment‐Reassembly StrategyAdvanced Synthesis & Catalysis, 356
S. Murahashi, T. Nakae, Hiroyuki Terai, Naruyoshi Komiya (2008)
Ruthenium-catalyzed oxidative cyanation of tertiary amines with molecular oxygen or hydrogen peroxide and sodium cyanide: sp3 C-H bond activation and carbon-carbon bond formation.Journal of the American Chemical Society, 130 33
J. Wencel‐Delord, F. Glorius (2013)
C-H bond activation enables the rapid construction and late-stage diversification of functional molecules.Nature chemistry, 5 5
D. DiRocco, T. Rovis (2012)
Catalytic asymmetric α-acylation of tertiary amines mediated by a dual catalysis mode: N-heterocyclic carbene and photoredox catalysis.Journal of the American Chemical Society, 134 19
S. Murahashi, Naruyoshi Komiya, Hiroyuki Terai (2005)
Ruthenium-catalyzed oxidative cyanation of tertiary amines with hydrogen peroxide and sodium cyanide.Angewandte Chemie, 44 42
Xuewang Gao, Qing-Yuan Meng, Minglin Xiang, Bin Chen, K. Feng, C. Tung, Lizhu Wu (2013)
Combining Visible Light Catalysis and Transition Metal Catalysis for the Alkylation of Secondary AminesAdvanced Synthesis & Catalysis, 355
Liang Zhao, Chao‐Jun Li (2008)
Functionalizing glycine derivatives by direct C-C bond formation.Angewandte Chemie, 47 37
Zhiping Li, D. Bohle, Chao‐Jun Li (2006)
Cu-catalyzed cross-dehydrogenative coupling: a versatile strategy for C-C bond formations via the oxidative activation of sp(3) C-H bonds.Proceedings of the National Academy of Sciences of the United States of America, 103 24
Wataru Muramatsu, Kimihiro Nakano, Chao‐Jun Li (2014)
Direct sp3 C-H bond arylation, alkylation, and amidation of tetrahydroisoquinolines mediated by hypervalent iodine(III) under mild conditions.Organic & biomolecular chemistry, 12 14
A well‐defined zinc antimonate salt was found to be an effective bifunctional catalyst that enables formal α‐CH bond functionalization of glycine derivatives via a sequential aerobic oxidation and allylation reaction.
Asian Journal of Organic Chemistry – Wiley
Published: Oct 1, 2014
Keywords: ; ; ; ;
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