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Journal articles on the topic 'Organopalladium compounds'

Author: Grafiati
Published: 4 June 2021
Last updated: 20 February 2023

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1

Massai, Lara, Thomas Scattolin, Matteo Tarchi, Fabiano Visentin, and Luigi Messori. "Reactions of proteins with a few organopalladium compounds of medicinal interest." RSC Advances 12, no. 41 (2022): 26680–85. http://dx.doi.org/10.1039/d2ra05332b.

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2

Larock, R. C. "New applications of organopalladium compounds in organic synthesis." Pure and Applied Chemistry 62, no. 4 (1990): 653–60. http://dx.doi.org/10.1351/pac199062040653.

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3

Takao, Yuko, Tokuji Takeda, Sachiko Tanikawa та Jun-ichiro Setsune. "Properties and reactions of μ-(dihydroxo)dipalladium(II) bisporphyrin complexes". Journal of Porphyrins and Phthalocyanines 07, № 07 (2003): 521–25. http://dx.doi.org/10.1142/s1088424603000653.

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μ-(dihydroxo)dipalladium(II) bisporphyrin was obtained by the reaction of dicationic bis(aqua)Pd(II) complexes of N21, N22-bridged porphyrin with NaOH or triethylamine. The reaction gives a mixture of two isomers and caused deprotonation from the active methylene compounds to give organopalladium(II) porphyrin complexes under neutral conditions.
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4

Biteau, Nicolas G., Vincent Roy, Cyril Nicolas, et al. "Synthesis and Structure–Activity Relationship Studies of Pyrido [1,2-E]Purine-2,4(1H,3H)-Dione Derivatives Targeting Flavin-Dependent Thymidylate Synthase in Mycobacterium Tuberculosis." Molecules 27, no. 19 (2022): 6216. http://dx.doi.org/10.3390/molecules27196216.

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In 2002, a new class of thymidylate synthase (TS) involved in the de novo synthesis of dTMP named Flavin-Dependent Thymidylate Synthase (FDTS) encoded by the thyX gene was discovered; FDTS is present only in 30% of prokaryote pathogens and not in human pathogens, which makes it an attractive target for the development of new antibacterial agents, especially against multi-resistant pathogens. We report herein the synthesis and structure-activity relationship of a novel series of hitherto unknown pyrido[1,2-E]purine-2,4(1H,3H)-dione analogues. Several synthetics efforts were done to optimize reg
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5

Rocha, Michelle C. da, Anderson M. Santana, Sandra R. Ananias, et al. "Citotoxicity and immune response induced by organopalladium(II) compounds in mice bearing Ehrlich ascites tumour." Journal of the Brazilian Chemical Society 18, no. 8 (2007): 1473–80. http://dx.doi.org/10.1590/s0103-50532007000800004.

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6

Li, Zhe, Lei Liu, Yao Fu, and Qing-Xiang Guo. "Assessing performance of diverse ONIOM methods in calculation of structures of organonickel and organopalladium compounds." Journal of Molecular Structure: THEOCHEM 757, no. 1-3 (2005): 69–76. http://dx.doi.org/10.1016/j.theochem.2005.07.014.

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7

Larock, Richard C., Kentaro Takagi, Joseph P. Burkhart, and Susan S. Hershberger. "Synthesis of polycyclic ketones via carbonylative cyclization of organopalladium compounds derived from norbornene and norbornadiene." Tetrahedron 42, no. 14 (1986): 3759–62. http://dx.doi.org/10.1016/s0040-4020(01)87528-1.

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8

Maassarani, Fida, Michel Pfeffer, and Guy Le Borgne. "Reactivity of cyclopalladated compounds. 23. Formal carbon-carbon triple-bond splitting in an organopalladium compound." Organometallics 9, no. 11 (1990): 3003–5. http://dx.doi.org/10.1021/om00161a034.

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9

Hashmi, A. Stephen K., Dominic Riedel, Marc A. Grundl, et al. "Bioconjugates of Enantiomerically Pure Organopalladium Compounds by Metal‐Assisted Positional Selective Transesterifications at Palladium Enolates." Chemistry – A European Journal 17, no. 23 (2011): 6407–14. http://dx.doi.org/10.1002/chem.201003308.

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10

Lohner, Pierre, Michel Pfeffer*, and Jean Fischer*. "Enlargement of the scope of the carbon–carbon coupling reactions between Fischer-type metallaalkylidyne and organopalladium compounds." Journal of Organometallic Chemistry 607, no. 1-2 (2000): 12–17. http://dx.doi.org/10.1016/s0022-328x(00)00108-x.

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11

Alsters, Paul L., Jaap Boersma, and Gerard van Koten. "Direct alkoxylation of organopalladium compounds based on a new type of C-O coupling mediated by molybdenum peroxides." Tetrahedron Letters 32, no. 5 (1991): 675–78. http://dx.doi.org/10.1016/s0040-4039(00)74857-x.

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12

ALSTERS, P. L., J. BOERSMA, and G. VAN KOTEN. "ChemInform Abstract: Direct Alkoxylation of Organopalladium Compounds Based on a New Type of C-O Coupling Mediated by Molybdenum Peroxides." ChemInform 22, no. 50 (2010): no. http://dx.doi.org/10.1002/chin.199150122.

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13

Alsters, Paul L., Jaap Boersma, and Gerard van Koten. "Reactivity of organopalladium compounds toward molybdenum peroxides: oxygen insertion versus carbon-chlorine and carbon-oxygen coupling. Evidence for palladium(IV) molybdate intermediates." Organometallics 12, no. 5 (1993): 1629–38. http://dx.doi.org/10.1021/om00029a022.

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14

Katsura, Tsutomu, Fuki Kato, and Kazuko Matsumoto. "Sensitivity enhancement by organopalladium complexes for graphite furnace atomic absorption spectrometry of alkyltin compounds in organic solvents and its application to the determination of total tin leached from ship paints." Analytica Chimica Acta 252, no. 1-2 (1991): 77–81. http://dx.doi.org/10.1016/0003-2670(91)87199-h.

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15

Maassarani, Fida, Michel Pfeffer, Guy Le Borgne, Johann T. B. H. Jastrzebski, and Gerard Van Koten. "Reactivity of cyclopalladated compounds. 13. Organopalladium compounds with a chiral palladated carbon atom. Facile isolation of optically active cyclopalladated complexes containing the (S)- or (R)-[2-Me2NC6H4CH(SiMe3)] monoanion. Molecular structure of [2-[1-(S)-(dimethylamino)ethyl]phenyl][2-(dimethylamino)-.alpha.-(trimethylsilyl)benzyl]palladium(II)." Organometallics 6, no. 5 (1987): 1111–18. http://dx.doi.org/10.1021/om00148a033.

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16

De La Puente, Pilar, Barbara Muz, Feda Azab, Micah John Luderer, Jack L. Arbiser, and Abdel Kareem Azab. "Tris DBA Palladium Overcomes Hypoxia Mediated Drug Resistance in Multiple Myeloma." Blood 126, no. 23 (2015): 2978. http://dx.doi.org/10.1182/blood.v126.23.2978.2978.

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Abstract Introduction: Despite recent progress in novel and targeted therapies, multiple myeloma (MM) remains a therapeutically challenging incurable disease. The regulation of important cellular processes and its link to cancer presented Src as an attractive target for MM. Src is a non-receptor protein tyrosine kinase which regulates multiple fundamental cellular processes including cell growth, migration, survival and differentiation. Activated Src in cancer lead to studies with Src as a target for anti-cancer drugs, and numerous Src inhibitors have become available to test the importance of
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17

USON, R., and J. FORNIES. "ChemInform Abstract: Organopalladium and Platinum Compounds with Pentahalophenyl Ligands." ChemInform 19, no. 50 (1988). http://dx.doi.org/10.1002/chin.198850331.

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18

Negishi, Ei-ichi. "Organopalladium Compounds Containing Pd(0) and Pd(II). General Discussion of the Methods of Synthesis and in situ Generation of Organopalladium Compounds." ChemInform 34, no. 31 (2003). http://dx.doi.org/10.1002/chin.200331263.

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19

LAROCK, R. C. "ChemInform Abstract: New Applications of Organopalladium Compounds in Organic Synthesis." ChemInform 21, no. 40 (1990). http://dx.doi.org/10.1002/chin.199040359.

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20

FOURNET, G., G. BALME, and J. GORE. "ChemInform Abstract: Intramolecular Nucleophilic Attack of Organopalladium Compounds in the Carbopalladation of Alkylidenecyclopropanes." ChemInform 19, no. 10 (1988). http://dx.doi.org/10.1002/chin.198810098.

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21

Choueiry, Daniele. "Stoichiometric Synthesis and Some Notable Properties of Organopalladium Compounds of Pd(0) and Pd(II)." ChemInform 34, no. 31 (2003). http://dx.doi.org/10.1002/chin.200331262.

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22

LAROCK, R. C., K. TAKAGI, J. P. BURKHART, and S. S. HERSHBERGER. "ChemInform Abstract: Synthesis of Polycyclic Ketones via Carbonylative Cyclization of Organopalladium Compounds Derived from Norbornene and Norbornadiene." Chemischer Informationsdienst 17, no. 48 (1986). http://dx.doi.org/10.1002/chin.198648148.

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23

LAROCK, R. C., та S. VARAPRATH. "ChemInform Abstract: MERCURY IN ORGANIC CHEMISTRY. 30. SYNTHESIS OF (Π-ALLYL)PALLADIUM COMPOUNDS VIA ORGANOPALLADIUM ADDITIONS TO ALKENYL- AND METHYLENECYCLOPROPANES AND ALKENYL- AND METHYLENECYCLOBUTANES". Chemischer Informationsdienst 16, № 8 (1985). http://dx.doi.org/10.1002/chin.198508296.

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