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Artículos de revistas sobre el tema "Chiral pincer ligands"

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Autor: Grafiati
Publicado: 11 de marzo de 2023

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1

Decken, Andreas, Robert A. Gossage y Paras N. Yadav. "Oxazoline chemistry. Part VIII. Synthesis and characterization of a new class of pincer ligands derived from the 2-(o-anilinyl)-2-oxazoline skeleton — Applications to the synthesis of group X transition metal catalysts". Canadian Journal of Chemistry 83, n.º 8 (1 de agosto de 2005): 1185–89. http://dx.doi.org/10.1139/v05-163.

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The synthesis and characterization of a new and readily synthesized class of potentially anionic pincer ligands with C1 point group symmetries is described. These materials can be made via amide coupling of a 2-(2′-anilinyl)-2-oxazoline unit with picolinic acid; the incorporation of enantiopure oxazoline fragments facilitates the construction of chiral C1 pincers. Treatment of the free ligands with Pd metal sources leads to the formation of amido–Pd pincer complexes in good yield. One of these Pd complexes has been characterized by single crystal X-ray diffraction methods, which confirms the proposed tridentate binding mode of the ligand and the formation of an amido N—Pd bond. The metal complexes have been shown to be suitable precusors for catalytically active Pd species that are useful for C—C bond forming reactions, notably the Heck reaction under standard conditions. Key words: oxazoline, 4,5-dihydro-2-oxazole, palladium, pincer ligand, amido, Heck reaction.
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2

Holzhacker, Christian, Berthold Stöger, Maria Deus Carvalho, Liliana P. Ferreira, Ernst Pittenauer, Günter Allmaier, Luis F. Veiros et al. "Synthesis and reactivity of TADDOL-based chiral Fe(ii) PNP pincer complexes-solution equilibria between κ2P,N- and κ3P,N,P-bound PNP pincer ligands". Dalton Transactions 44, n.º 29 (2015): 13071–86. http://dx.doi.org/10.1039/c5dt00832h.

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3

Zivkovic, Kristina, Lilia M. Baldauf, Jessica L. Cryder, Alexa Villaseñor, Valeria Reyes, Lauren E. Bernier, Theresa J. Thomas et al. "Chiral tridentate bis(oxazol-2-ylimino) isoindoline-based pincer ligands: isolation and characterization via deligation from in situ prepared Cd-ligand complexes". Dalton Transactions 50, n.º 29 (2021): 10041–49. http://dx.doi.org/10.1039/d0dt02531c.

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4

Felluga, Fulvia, Walter Baratta, Lidia Fanfoni, Giuliana Pitacco, Pierluigi Rigo y Fabio Benedetti. "Efficient Chemoenzymatic Synthesis of Chiral Pincer Ligands". Journal of Organic Chemistry 74, n.º 9 (mayo de 2009): 3547–50. http://dx.doi.org/10.1021/jo900271x.

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5

Cohen, Orit, Olga Grossman, Luigi Vaccaro y Dmitri Gelman. "Synthesis of chiral nonracemic PC(sp3)P pincer ligands". Journal of Organometallic Chemistry 750 (enero de 2014): 13–16. http://dx.doi.org/10.1016/j.jorganchem.2013.10.051.

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6

Deng, Qing-Hai, Rebecca L. Melen y Lutz H. Gade. "Anionic Chiral Tridentate N-Donor Pincer Ligands in Asymmetric Catalysis". Accounts of Chemical Research 47, n.º 10 (28 de agosto de 2014): 3162–73. http://dx.doi.org/10.1021/ar5002457.

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7

Zhao, Ning, Guohua Hou, Xuebin Deng, Guofu Zi y Marc D. Walter. "Group 4 metal complexes with new chiral pincer NHC-ligands: synthesis, structure and catalytic activity". Dalton Trans. 43, n.º 22 (2014): 8261–72. http://dx.doi.org/10.1039/c4dt00510d.

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8

Albrecht, Martin, Betty M. Kocks, Anthony L. Spek y Gerard van Koten. "Chiral platinum and palladium complexes containing functionalized C2-symmetric bisaminoaryl ‘Pincer’ ligands". Journal of Organometallic Chemistry 624, n.º 1-2 (abril de 2001): 271–86. http://dx.doi.org/10.1016/s0022-328x(01)00667-2.

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9

Deng, Qing-Hai, Rebecca L. Melen y Lutz H. Gade. "ChemInform Abstract: Anionic Chiral Tridentate N-Donor Pincer Ligands in Asymmetric Catalysis". ChemInform 45, n.º 52 (11 de diciembre de 2014): no. http://dx.doi.org/10.1002/chin.201452242.

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10

Konrad, Felix, Julio Lloret Fillol, Hubert Wadepohl y Lutz H. Gade. "Bis(oxazolinylmethyl)pyrrole Derivatives and Their Coordination as Chiral “Pincer” Ligands to Rhodium". Inorganic Chemistry 48, n.º 17 (7 de septiembre de 2009): 8523–35. http://dx.doi.org/10.1021/ic901189k.

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11

Bonnet, Sylvestre, Jie Li, Maxime A Siegler, Lars S von Chrzanowski, Anthony L Spek, Gerard van Koten y Robertus J. M. Klein Gebbink. "Synthesis and Resolution of Planar-Chiral Ruthenium-Palladium Complexes with ECE′ Pincer Ligands". Chemistry - A European Journal 15, n.º 14 (23 de marzo de 2009): 3340–43. http://dx.doi.org/10.1002/chem.200900117.

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12

Partl, Gabriel Julian, Felix Nussbaumer, Walter Schuh, Holger Kopacka, Klaus Wurst y Paul Peringer. "Crystal structures of two PCN pincer iridium complexes and one PCP pincer carbodiphosphorane iridium intermediate: substitution of one phosphine moiety of a carbodiphosphorane by an organic azide". Acta Crystallographica Section E Crystallographic Communications 75, n.º 1 (1 de enero de 2019): 75–80. http://dx.doi.org/10.1107/s2056989018017644.

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The structure of [Ir{(4-Cl-C6H4N3)C(dppm)-κ3 P,C,N}(dppm-κ2 P,P′)]Cl·1.5CH2Cl2·0.5C7H8 (C57H48Cl2IrN3P4·1.5CH2Cl2·0.5C7H8) (2), dppm = bis(diphenylphosphino)methane {systematic name: [7-(4-chlorophenyl)-1,1,3,3-tetraphenyl-5,6,7-triaza-κN 7-1,3λ4-diphospha-κP 1-hepta-4,6-dien-4-yl][methylenebis(diphenylphosphine)-κ2 P,P′]iridium(I) chloride–dichloromethane–toluene (2/3/1)}, resulting from the reaction of [IrClH{C(dppm)2-κ3 P,C,P)(MeCN)]Cl (1a) with 1-azido-4-chlorobenzene, shows a monocationic five-coordinate IrI complex with a distorted trigonal–bipyramidal geometry. In 2, the iridium centre is coordinated by the neutral triazeneylidenephosphorane (4-Cl-C6H4N3)C(dppm) acting as a PCN pincer ligand, and a chelating dppm unit. The structure of the coordination compound [IrCl(CN)H(C(dppm)2-κ3 P,C,P)]·CH3CN, (C52H45ClIrNP4·CH3CN) (1b) [systematic name: chloridocyanidohydrido(1,1,3,3,5,5,7,7-octaphenyl-1,3λ5,5λ4,7-tetraphospha-κ2 P 1,P 7-hept-3-en-4-yl)iridium(III) acetonitrile monosolvate], prepared from 1a and KCN, reveals an octahedral IrIII central atom with a meridional PCP pincer carbodiphosphorane (CDP) ligand; the chloride ligand is located trans to the central carbon of the CDP functionality while the hydrido and cyanido ligands are situated trans to each other. The chiral coordination compound [Ir(CN)((4-Cl-C6H4N3)CH(CH(P(Ph)2)2)-κ3 P,C,N)(dppm-κ2 P,P′)]·2CH3OH, (C58H48ClIrN4P4·2CH3OH) (3) (systematic name: {4-[3-(4-chlorophenyl)triazenido-κN 3]-1,1,3,3-tetraphenyl-1,3λ5-diphospha-κP 1-but-2-en-4-yl}cyanido[methylenebis(diphenylphosphine)-κ2 P,P′]iridium(III) methanol disolvate), formed via prolonged reaction of 1-azido-4-chlorobenzene with 1b, features a six-coordinate IrIII central atom. The iridium centre is coordinated by the dianionic facial PCN pincer ligand [(4-Cl-C6H4N3)CH(CH(P(Ph2)2)2)], a cyanido ligand trans to the central carbon of the PCN pincer ligand and a chelating dppm unit. Complex 2 exhibits a 2:1 positional disorder of the Cl− anion. The CH2Cl2 and C7H8 solvent molecules show occupational disorder, with the toluene molecule exhibiting additional 1:1 positional disorder with some nearly overlying carbon atoms.
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13

Radchenko, Yana, Shrouq Mujahed, Sanaa Musa y Dmitri Gelman. "Synthesis and characterization of chiral enantiopure PC(sp)P pincer ligands and their complexes". Inorganica Chimica Acta 521 (junio de 2021): 120350. http://dx.doi.org/10.1016/j.ica.2021.120350.

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14

Albrecht, Martin, Betty M. Kocks, Anthony L. Spek y Gerard van Koten. "Erratum to: “Chiral platinum and palladium complexes containing functionalized C2-symmetric bisaminoaryl ‘Pincer’ ligands”". Journal of Organometallic Chemistry 630, n.º 2 (julio de 2001): 281. http://dx.doi.org/10.1016/s0022-328x(01)00986-x.

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15

Langlotz, Björn K, Hubert Wadepohl y Lutz H Gade. "Chiral Bis(pyridylimino)isoindoles: A Highly Modular Class of Pincer Ligands for Enantioselective Catalysis". Angewandte Chemie 120, n.º 25 (9 de junio de 2008): 4748–52. http://dx.doi.org/10.1002/ange.200801150.

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16

Langlotz, Björn K, Hubert Wadepohl y Lutz H Gade. "Chiral Bis(pyridylimino)isoindoles: A Highly Modular Class of Pincer Ligands for Enantioselective Catalysis". Angewandte Chemie International Edition 47, n.º 25 (9 de junio de 2008): 4670–74. http://dx.doi.org/10.1002/anie.200801150.

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17

Wu, Dunqi, Xuan Cheng, Yankai Liu, Guo Cheng, Xiaoyu Guan y Qinghai Deng. "A New Class of Chiral Pincer-Type PNN Ligands for Pd-Catalyzed Asymmetric Allylic Alkylation". Chinese Journal of Organic Chemistry 40, n.º 10 (2020): 3362. http://dx.doi.org/10.6023/cjoc202005090.

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18

Zirakzadeh, Afrooz, Karl Kirchner, Alexander Roller, Berthold Stöger, Michael Widhalm y Robert H. Morris. "Iron(II) Complexes Containing Chiral Unsymmetrical PNP′ Pincer Ligands: Synthesis and Application in Asymmetric Hydrogenations". Organometallics 35, n.º 21 (4 de noviembre de 2016): 3781–87. http://dx.doi.org/10.1021/acs.organomet.6b00711.

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19

Bootsma, Johan, Beibei Guo, Johannes G. de Vries y Edwin Otten. "Ruthenium Complexes with PNN Pincer Ligands Based on (Chiral) Pyrrolidines: Synthesis, Structure, and Dynamic Stereochemistry". Organometallics 39, n.º 4 (5 de febrero de 2020): 544–55. http://dx.doi.org/10.1021/acs.organomet.9b00765.

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20

Grüger, Nora, Lara-Isabel Rodríguez, Hubert Wadepohl y Lutz H. Gade. "Achiral and Chiral PNP-Pincer Ligands with a Carbazole Backbone: Coordination Chemistry with d8 Transition Metals". Inorganic Chemistry 52, n.º 4 (30 de enero de 2013): 2050–59. http://dx.doi.org/10.1021/ic302454n.

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21

Marcum, Justin S., Courtney C. Roberts, Rajith S. Manan, Tia N. Cervarich y Simon J. Meek. "Chiral Pincer Carbodicarbene Ligands for Enantioselective Rhodium-Catalyzed Hydroarylation of Terminal and Internal 1,3-Dienes with Indoles". Journal of the American Chemical Society 139, n.º 44 (26 de octubre de 2017): 15580–83. http://dx.doi.org/10.1021/jacs.7b08575.

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22

Benito-Garagorri, David, Eva Becker, Julia Wiedermann, Wolfgang Lackner, Martin Pollak, Kurt Mereiter, Joanna Kisala y Karl Kirchner. "Achiral and Chiral Transition Metal Complexes with Modularly Designed Tridentate PNP Pincer-Type Ligands Based on N-Heterocyclic Diamines". Organometallics 25, n.º 8 (abril de 2006): 1900–1913. http://dx.doi.org/10.1021/om0600644.

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23

Hyodo, Kengo, Shuichi Nakamura y Norio Shibata. "Enantioselective Aza-Morita-Baylis-Hillman Reactions of Acrylonitrile Catalyzed by Palladium(II) Pincer Complexes havingC2-Symmetric Chiral Bis(imidazoline) Ligands". Angewandte Chemie International Edition 51, n.º 41 (17 de septiembre de 2012): 10337–41. http://dx.doi.org/10.1002/anie.201204891.

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24

Hyodo, Kengo, Shuichi Nakamura y Norio Shibata. "Enantioselective Aza-Morita-Baylis-Hillman Reactions of Acrylonitrile Catalyzed by Palladium(II) Pincer Complexes havingC2-Symmetric Chiral Bis(imidazoline) Ligands". Angewandte Chemie 124, n.º 41 (17 de septiembre de 2012): 10483–87. http://dx.doi.org/10.1002/ange.201204891.

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25

Yan, Jing, Yan-Bing Wang, Zhi-Hui Zhu, Yigao Li, Xinju Zhu, Xin-Qi Hao y Mao-Ping Song. "Synthesis, Characterization, and Catalytic Studies of Unsymmetrical Chiral NCC Pincer Pd(II) and Ni(II) Complexes Bearing (Imidazolinyl)aryl NHC Ligands". Organometallics 37, n.º 14 (3 de julio de 2018): 2325–34. http://dx.doi.org/10.1021/acs.organomet.8b00300.

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26

Wang, Tao, Jun-Long Niu, Shuang-Liang Liu, Juan-Juan Huang, Jun-Fang Gong y Mao-Ping Song. "Chiral NCN Pincer Rhodium(III) Complexes with Bis(imidazolinyl)phenyl Ligands: Synthesis and Enantioselective Catalytic Alkynylation of Trifluoropyruvates with Terminal Alkynes". Advanced Synthesis & Catalysis 355, n.º 5 (28 de febrero de 2013): 927–37. http://dx.doi.org/10.1002/adsc.201200967.

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27

Zhang, Ben-Shang, Wei Wang, Dan-Dan Shao, Xin-Qi Hao, Jun-Fang Gong y Mao-Ping Song. "Unsymmetrical Chiral PCN Pincer Palladium(II) and Nickel(II) Complexes of (Imidazolinyl)aryl Phosphinite Ligands: Synthesis via Ligand C−H Activation, Crystal Structures, and Catalytic Studies". Organometallics 29, n.º 11 (14 de junio de 2010): 2579–87. http://dx.doi.org/10.1021/om100232n.

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28

Borisova, N. E., F. E. Zhurkin, T. G. Gulevich, K. K. Babievskii, M. D. Reshetova y V. A. Knizhnikov. "Pincer ligands based on α-amino acids: V. New generation chiral receptors for the recognition of amino acid enantiomers in aqueous environment". Russian Journal of Organic Chemistry 47, n.º 2 (febrero de 2011): 193–201. http://dx.doi.org/10.1134/s1070428011020072.

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29

Lu, Zhengliang, Srinivas Abbina, Jared R. Sabin, Victor N. Nemykin y Guodong Du. "Unexpected Formation of Chiral Pincer CNN Nickel Complexes with β-Diketiminato Type Ligands via C–H Activation: Synthesis, Properties, Structures, and Computational Studies". Inorganic Chemistry 52, n.º 3 (15 de enero de 2013): 1454–65. http://dx.doi.org/10.1021/ic3021904.

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30

Wang, Tao, Jun-Long Niu, Shuang-Liang Liu, Juan-Juan Huang, Jun-Fang Gong y Mao-Ping Song. "ChemInform Abstract: Chiral NCN Pincer Rhodium(III) Complexes with Bis(imidazolinyl)phenyl Ligands: Synthesis and Enantioselective Catalytic Alkynylation of Trifluoropyruvates with Terminal Alkynes." ChemInform 44, n.º 31 (11 de julio de 2013): no. http://dx.doi.org/10.1002/chin.201331036.

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31

Deng, Qing-Hai, Hubert Wadepohl y Lutz H. Gade. "The Synthesis of a New Class of Chiral Pincer Ligands and Their Applications in Enantioselective Catalytic Fluorinations and the Nozaki-Hiyama-Kishi Reaction". Chemistry - A European Journal 17, n.º 52 (3 de noviembre de 2011): 14922–28. http://dx.doi.org/10.1002/chem.201102375.

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32

Hyodo, Kengo, Shuichi Nakamura y Norio Shibata. "ChemInform Abstract: Enantioselective Aza-Morita-Baylis-Hillman Reactions of Acrylonitrile Catalyzed by Palladium(II) Pincer Complexes Having C2-Symmetric Chiral Bis(imidazoline) Ligands." ChemInform 44, n.º 11 (8 de marzo de 2013): no. http://dx.doi.org/10.1002/chin.201311075.

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33

Deng, Qing-Hai, Hubert Wadepohl y Lutz H. Gade. "ChemInform Abstract: The Synthesis of a New Class of Chiral Pincer Ligands and Their Applications in Enantioselective Catalytic Fluorinations and the Nozaki-Hiyama-Kishi Reaction." ChemInform 43, n.º 20 (23 de abril de 2012): no. http://dx.doi.org/10.1002/chin.201220021.

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34

Li, Nan, Wen-Jing Zhu, Juan-Juan Huang, Xin-Qi Hao, Jun-Fang Gong y Mao-Ping Song. "Chiral NCN Pincer Iridium(III) Complexes with Bis(imidazolinyl)phenyl Ligands: Synthesis and Application in Enantioselective C–H Functionalization of Indoles with α-Aryl-α-diazoacetates". Organometallics 39, n.º 12 (4 de junio de 2020): 2222–34. http://dx.doi.org/10.1021/acs.organomet.0c00174.

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35

Wang, Tao, Xin-Qi Hao, Juan-Juan Huang, Kai Wang, Jun-Fang Gong y Mao-Ping Song. "Chiral CNN Pincer Palladium(II) Complexes with 2-Aryl-6-(oxazolinyl)pyridine Ligands: Synthesis, Characterization, and Application to Enantioselective Allylation of Isatins and Suzuki–Miyaura Coupling Reaction". Organometallics 33, n.º 1 (11 de diciembre de 2013): 194–205. http://dx.doi.org/10.1021/om400945d.

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36

Chen, Ran, Qian-Qian Yan, Shao-Jun Hu, Xiao-Qing Guo, Li-Xuan Cai, Dan-Ni Yan, Li-Peng Zhou y Qing-Fu Sun. "Dinuclear helicate or mononuclear pincer lanthanide complexes from one ligand: stereo-controlled assembly and catalysis". Organic Chemistry Frontiers 8, n.º 11 (2021): 2576–82. http://dx.doi.org/10.1039/d1qo00369k.

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By varying the metal/ligand ratio, either dinuclear triple helicate or mononuclear pincer can be stereo-selectively obtained from the same chiral ligand. Their catalytic properties have been demonstrated with the asymmetric FC alkylation reactions.
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37

Yang, Ming-Jun, Yan-Jing Liu, Jun-Fang Gong y Mao-Ping Song. "Unsymmetrical Chiral PCN Pincer Palladium(II) and Nickel(II) Complexes with Aryl-Based Aminophosphine–Imidazoline Ligands: Synthesis via Aryl C–H Activation and Asymmetric Addition of Diarylphosphines to Enones". Organometallics 30, n.º 14 (25 de julio de 2011): 3793–803. http://dx.doi.org/10.1021/om200350h.

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38

Deak, Noemi, Olivier Thillaye du Boullay, Ionut-Tudor Moraru, Sonia Mallet-Ladeira, David Madec y Gabriela Nemes. "A non-symmetric sulfur-based O,C,O-chelating pincer ligand leading to chiral germylene and stannylene". Dalton Transactions 48, n.º 7 (2019): 2399–406. http://dx.doi.org/10.1039/c8dt05116j.

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39

Gavrilov, K. N., E. A. Rastorguev, A. A. Shiryaev, T. B. Grishina, A. S. Safronov, S. E. Lyubimov y V. A. Davankov. "The first pincer-type phosphodiamidite ligand containing chiral phosphorus atoms". Russian Chemical Bulletin 58, n.º 6 (junio de 2009): 1325–27. http://dx.doi.org/10.1007/s11172-009-0176-2.

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40

Baber, R. Angharad, Robin B. Bedford, Michael Betham, Michael E. Blake, Simon J. Coles, Mairi F. Haddow, Michael B. Hursthouse et al. "Chiral palladium bis(phosphite) PCP-pincer complexes via ligand C–H activation". Chem. Commun., n.º 37 (2006): 3880–82. http://dx.doi.org/10.1039/b609704a.

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41

Gavrilov, K. N., E. A. Rastorguev, A. A. Shiryaev, T. B. Grishina, A. S. Safronov, S. E. Lyubimov y V. A. Davankov. "ChemInform Abstract: The First Pincer-Type Phosphodiamidite Ligand Containing Chiral Phosphorus Atoms." ChemInform 41, n.º 41 (16 de septiembre de 2010): no. http://dx.doi.org/10.1002/chin.201041030.

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42

Garbe, Marcel, Kathrin Junge, Svenja Walker, Zhihong Wei, Haijun Jiao, Anke Spannenberg, Stephan Bachmann, Michelangelo Scalone y Matthias Beller. "Manganese(I)-Catalyzed Enantioselective Hydrogenation of Ketones Using a Defined Chiral PNP Pincer Ligand". Angewandte Chemie International Edition 56, n.º 37 (18 de agosto de 2017): 11237–41. http://dx.doi.org/10.1002/anie.201705471.

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43

Garbe, Marcel, Kathrin Junge, Svenja Walker, Zhihong Wei, Haijun Jiao, Anke Spannenberg, Stephan Bachmann, Michelangelo Scalone y Matthias Beller. "Manganese(I)-Catalyzed Enantioselective Hydrogenation of Ketones Using a Defined Chiral PNP Pincer Ligand". Angewandte Chemie 129, n.º 37 (18 de agosto de 2017): 11389–93. http://dx.doi.org/10.1002/ange.201705471.

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44

Garbe, Marcel, Zhihong Wei, Bianca Tannert, Anke Spannenberg, Haijun Jiao, Stephan Bachmann, Michelangelo Scalone, Kathrin Junge y Matthias Beller. "Enantioselective Hydrogenation of Ketones using Different Metal Complexes with a Chiral PNP Pincer Ligand". Advanced Synthesis & Catalysis 361, n.º 8 (5 de marzo de 2019): 1913–20. http://dx.doi.org/10.1002/adsc.201801511.

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45

Kuznetsov, Vladimir F., Alan J. Lough y Dmitry G. Gusev. "Palladium and rhodium complexes of a chiral pincer ligand derived from 1,3-trans disubstituted cyclohexane". Inorganica Chimica Acta 359, n.º 9 (junio de 2006): 2806–11. http://dx.doi.org/10.1016/j.ica.2005.11.010.

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46

Bedford, Robin B., Yu-Ning Chang, Mairi F. Haddow y Claire L. McMullin. "Tuning ligand structure in chiral bis(phosphite) and mixed phosphite–phosphinite PCP-palladium pincer complexes". Dalton Transactions 40, n.º 35 (2011): 9034. http://dx.doi.org/10.1039/c1dt10356c.

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Hao, Xin-Qi, Ya-Nan Wang, Jun-Rui Liu, Kun-Lun Wang, Jun-Fang Gong y Mao-Ping Song. "Unsymmetrical, oxazolinyl-containing achiral and chiral NCN pincer ligand precursors and their complexes with palladium(II)". Journal of Organometallic Chemistry 695, n.º 1 (enero de 2010): 82–89. http://dx.doi.org/10.1016/j.jorganchem.2009.09.031.

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Qian, Lu, Xixia Tang, Zhidao Huang, Yulei Wang, Guixia Liu y Zheng Huang. "Chiral Iridium Complexes of Anionic NCP Pincer Ligand for Asymmetric Transfer Hydrogenation of 1,1-Diarylethenes with Ethanol". Organic Letters 23, n.º 22 (8 de noviembre de 2021): 8978–83. http://dx.doi.org/10.1021/acs.orglett.1c03455.

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Cryder, Jessica L., Andrew J. Killgore, Curtis Moore, James A. Golen, Arnold L. Rheingold y Christopher J. A. Daley. "Novel metal complexes containing a chiral trinitrogen isoindoline-based pincer ligand: in situ synthesis and structural characterization". Dalton Transactions 39, n.º 44 (2010): 10671. http://dx.doi.org/10.1039/c0dt00869a.

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Motoyama, Yukihiro, Kayoko Shimozono y Hisao Nishiyama. "Novel (oxazolinyl)phenyl phosphinite pincer ligand: Development of the first non-symmetrical, PCN type chiral palladium and platinum complexes". Inorganica Chimica Acta 359, n.º 6 (abril de 2006): 1725–30. http://dx.doi.org/10.1016/j.ica.2005.06.034.

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