Academic literature on the topic 'BINAP'

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Journal articles on the topic "BINAP"

1

Ohkuma, Takeshi, and Nobuhito Kurono. "ChemInform Abstract: BINAP." ChemInform 42, no. 50 (2011): no. http://dx.doi.org/10.1002/chin.201150221.

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2

Wheaton, Craig A., Michael C. Jennings, and Richard J. Puddephatt. "Complexes of Gold(I) with a Chiral Diphosphine Ligand: A Polymer with Both Au···Ag and Ag···Ag Metallophilic Bonds." Zeitschrift für Naturforschung B 64, no. 11-12 (2009): 1469–77. http://dx.doi.org/10.1515/znb-2009-11-1230.

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The chemistry of gold(I) with the ligand binap = 2,2'-bis(diphenylphosphino)-1,1' -binaphthyl is reported. Reaction of [Au2Cl2(μ-binap)] with silver trifluoroacetate gave the corresponding complex [Au2(O2CCF3)2(μ-binap)], and crystallization in the presence of excess silver trifluoroacetate gave the unusual syndiotactic polymeric complex [{Au2Ag2(μ-O2CCF3)4(μ-binap)}n], which contains both Au・ ・ ・Ag and Ag・ ・ ・Ag metallophilic bonds. The trifluoroacetate ligands in [Au2(O2CCF3)2(μ- binap)] can be replaced by nitrogen or phosphorus donor ligands to give complexes [Au2(κ1-4,4'- bipyridine)2(μ-bi
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3

Shekhar, Shashank, Per Ryberg, and John F. Hartwig. "Oxidative Addition of Phenyl Bromide to Pd(BINAP) vs Pd(BINAP)(amine). Evidence for Addition to Pd(BINAP)." Organic Letters 8, no. 5 (2006): 851–54. http://dx.doi.org/10.1021/ol0528890.

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4

Gibson, Susan E., Karina A. C. Kaufmann, Jennifer A. Loch, and Ayako Miyazaki. "Metal carbonyl complexes and chirality." Pure and Applied Chemistry 80, no. 5 (2008): 903–11. http://dx.doi.org/10.1351/pac200880050903.

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A study of the Pauson-Khand reaction (PKR) based on Co2(CO)8 and binap has revealed that a key precatalyst is (binap)Co2(CO)6, and that alkynes add to this species to generate isomers that interconvert under typical PKR conditions. A 31P NMR study of (binap)(N-(prop-2-enyl)-N-(prop-2-ynyl)-p-toluenesulfonamide)Co2(CO)4 revealed that heating this species gives rise to an unexpected cobalt hydride species (binap)Co(CO)2H together with (binap)Co2(CO)6. Observation of a PKR reaction by 31P NMR spectroscopy revealed that the hydride species is generated during the course of the reaction.
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5

Kono, Yuki, Kazuki Nakabayashi, Sayaka Kitamura, Reiko Kuroda, Michiya Fujiki, and Yoshitane Imai. "A comparison of circularly polarised luminescent BINAP and BINAPO as chiral binaphthyl luminophores." Tetrahedron 71, no. 23 (2015): 3985–89. http://dx.doi.org/10.1016/j.tet.2015.04.048.

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6

Arshad, Nuzhat, and C. Oliver Kappe. "ChemInform Abstract: Heterocyclic BINAP Analogues." ChemInform 41, no. 28 (2010): no. http://dx.doi.org/10.1002/chin.201028260.

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7

Wu, Peng, Guojun Deng, Qinghua Fan, et al. "Assembling Behavior of BINAP Derivative." Chemistry Letters 31, no. 7 (2002): 706–7. http://dx.doi.org/10.1246/cl.2002.706.

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8

Zarate, Ximena, Eduardo Schott, Rodrigo Ramirez-Tagle, Desmond MacLeod-Carey, and Ramiro Arratia-Pérez. "Photophysical properties of [Cu(binap)2]+ and [Pd(binap)2] complexes: A theoretical study." Polyhedron 37, no. 1 (2012): 54–59. http://dx.doi.org/10.1016/j.poly.2012.02.009.

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9

Wöste, Thorsten H., and Martin Oestreich. "BINAP versus BINAP(O) in Asymmetric Intermolecular Mizoroki-Heck Reactions: Substantial Effects on Selectivities." Chemistry - A European Journal 17, no. 42 (2011): 11914–18. http://dx.doi.org/10.1002/chem.201101695.

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10

Tominaga, Hiroshi, Ken Sakai, and Taro Tsubomura. "Structure and photophysical properties of [Pt0(binap)2][binap = 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl]." J. Chem. Soc., Chem. Commun., no. 22 (1995): 2273–74. http://dx.doi.org/10.1039/c39950002273.

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