Relevant bibliographies by topics / Tetrakis(triphenylphosphine)nickel(0)

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Academic literature on the topic 'Tetrakis(triphenylphosphine)nickel(0)'

Author: Grafiati
Published: 4 June 2021
Last updated: 13 February 2022

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Journal articles on the topic "Tetrakis(triphenylphosphine)nickel(0)"

1

Čermák, Jan, Vratislav Blechta, and Václav Chvalovský. "Cooligomerization of propadiene with propyne catalysed by nickel(0) complexes." Collection of Czechoslovak Chemical Communications 53, no. 6 (1988): 1274–86. http://dx.doi.org/10.1135/cccc19881274.

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Cooligomerization of propadiene with propyne catalysed by bis(1,5-cyclooctadiene)nickel and tetrakis(triphenylphosphine)nickel gives a variety of products, including besides the cooligomers also the homooligomers of both monomers. The type of catalyst affects partially the product distribution due to changes in the degree of oligomerization. Cooligomerization of propadiene with 3-deuteriopropyne provided information about relative proportion of propadiene and propyne units in the oligomers.
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2

Ramaotsoa, G. Valerie, Ian Strydom, Jenny-Lee Panayides, and Darren Riley. "Immobilized tetrakis(triphenylphosphine)palladium(0) for Suzuki–Miyaura coupling reactions under flow conditions." Reaction Chemistry & Engineering 4, no. 2 (2019): 372–82. http://dx.doi.org/10.1039/c8re00235e.

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An immobilized triphenylphosphine scaffold was prepared by precipitation polymerization and functionalized to afford a cost-effective source of solid-supported tetrakis(triphenylphosphine)palladium(0).
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3

Avent, Anthony G., F. Goeffrey N. Cloke, Jeremy P. Day, Elaine A. Seddon, Kenneth R. Seddon, and Stephen M. Smedley. "Tetrakis(trimethylphosphine)nickel(0)." Journal of Organometallic Chemistry 341, no. 1-3 (1988): 535–41. http://dx.doi.org/10.1016/0022-328x(88)89106-x.

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4

Crayston, J. A., and G. Davidson. "Vibrational spectroscope of complexes of platinum(0)—I. Tetrakis(triphenylphosphine)platinum(0) and Dioxygenbis(triphenylphosphine)platinum(0)." Spectrochimica Acta Part A: Molecular Spectroscopy 42, no. 11 (1986): 1311–16. http://dx.doi.org/10.1016/0584-8539(86)80232-x.

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5

Zhou, Qi-Lin, and Yao-Zeng Huang. "Direct fluoroalkylation of aromatic compounds catalyzed by tetrakis(triphenylphosphine)nickel." Journal of Fluorine Chemistry 43, no. 3 (1989): 385–92. http://dx.doi.org/10.1016/s0022-1139(00)82725-6.

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6

Xu, Jie, and Peter Wipf. "Indole synthesis by palladium-catalyzed tandem allylic isomerization – furan Diels–Alder reaction." Organic & Biomolecular Chemistry 15, no. 34 (2017): 7093–96. http://dx.doi.org/10.1039/c7ob01654a.

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7

Plinta, Hans-Jürgen, Robert Gereke, Axel Fischer, Peter G. Jones, and Reinhard Schmutzler. "Darstellung und Reaktionen von zweikernigen Platin(II)-Komplexen; Einkristall-Röntgenstrukturanalyse eines Tetrakis(difluorphosphonato)-Palladat(II)-Komplexes / Preparation and Reactions of Binuclear Platinum(II) Complexes. Single Crystal X-Ray Diffraction Study of a Tetrakis(difluorophosphonato)palladate(II) Complex." Zeitschrift für Naturforschung B 48, no. 6 (1993): 737–46. http://dx.doi.org/10.1515/znb-1993-0607.

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o-Methylbenzyldifluorophosphite 2 was obtained by the reaction of o-methylbenzyltrimethyl silyl ether 1 with chlorodifluorophosphine PF2Cl. The reaction of 2 with the palladium(II) complex 3 led to the tetrakis(difluorophosphonato)palladate(II) complex 7. The X-ray structure analysis of 7 confirmed the nearly exact square planar structure at the metal atom of the tetrakis(difluorophosphonato)palladate(II) dianion. Minimal deviations from the ideal geometry at palladium and phosphorus are mainly the result of thermal motion or disorder phenomena in the crystal. In the reaction of the platinum(I
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8

Cai, Ming-Zhong, Chun-Yun Peng, Hong Zhao, and Jia-Di Huang. "Stereoselective Synthesis of 1,3-enynylselenides via Palladium-Catalysed Cross Coupling Reactions." Journal of Chemical Research 2002, no. 8 (2002): 376–77. http://dx.doi.org/10.3184/030823402103172365.

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( E)-α-Bromovinylselenides undergo a cross coupling reaction with alkynyl Grignard reagents in the presence of tetrakis(triphenylphosphine)palladium(0) in THF at room temperature to afford 1,3-enynylselenides in good yields.
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9

Cai, Mingzhong, Wenyan Hao, Hong Zhao, and Caisheng Song. "Stereoselective Synthesis of 1,3-Enynylsilanes via Hydromagnesiation Reaction of Alkynylsilanes." Journal of Chemical Research 2003, no. 8 (2003): 485–86. http://dx.doi.org/10.3184/030823403103174623.

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Hydromagnesiation of alkynylsilanes gives ( Z)-α-silylvinyl Grignard reagents, which are cross-coupled with alkynyl iodides in the presence of tetrakis(triphenylphosphine)palladium(0) catalyst to afford stereoselectively 1,3-enynylsilanes in good yields.
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10

Piers, Edward, та Fraser F. Fleming. "Palladium(0)-catalyzed conversion of vinyl trifluoromethanesulfonates into α,β-unsaturated nitriles". Canadian Journal of Chemistry 71, № 11 (1993): 1867–72. http://dx.doi.org/10.1139/v93-234.

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Treatment (benzene, room temperature) of each of the vinyl trifluoromethanesulfonates 16–23 with dry lithium cyanide in the presence of catalytic amounts of tetrakis(triphenylphosphine)palladium(0) and the crown ether 12-crown-4 provides good to excellent yields of the corresponding α,β-unsaturated nitriles 24–31.
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