Artykuły w czasopismach na temat „Multinuclear organotin”
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Sprawdź 37 najlepszych artykułów w czasopismach naukowych na temat „Multinuclear organotin”.
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Cherryman, Julian C., i Robin K. Harris. "New Multinuclear Experiments on Solid Organotin Fluorides". Journal of Magnetic Resonance 128, nr 1 (wrzesień 1997): 21–29. http://dx.doi.org/10.1006/jmre.1997.1206.
Pełny tekst źródłaRashid, Faisal, Noor Uddin, Saqib Ali, Ali Haider, Syed Ahmad Tirmizi, Paula L. Diaconescu i Jamshed Iqbal. "New triorganotin(iv) compounds with aromatic carboxylate ligands: synthesis and evaluation of the pro-apoptotic mechanism". RSC Advances 11, nr 8 (2021): 4499–514. http://dx.doi.org/10.1039/d0ra06695h.
Pełny tekst źródłaMatela, Garima, i Robina Aman. "Organotin(IV) complexes of carboxylic acid derivatives". Open Chemistry 10, nr 1 (1.02.2012): 1–15. http://dx.doi.org/10.2478/s11532-011-0107-6.
Pełny tekst źródłaTagne Kuate, Alain C., Roger A. Lalancette i F. Jäkle. "Planar-chiral ferrocenylphosphine-borane complexes featuring agostic-type B–H⋯E (E = Hg, Sn) interactions". Dalton Transactions 46, nr 19 (2017): 6253–64. http://dx.doi.org/10.1039/c6dt04791b.
Pełny tekst źródłaSingh, Har Lal, i A. K. Varshney. "Synthetic, Structural, and Biochemical Studies of Organotin(IV) with Schiff Bases Having Nitrogen and Sulphur Donor Ligands". Bioinorganic Chemistry and Applications 2006 (2006): 1–7. http://dx.doi.org/10.1155/bca/2006/23245.
Pełny tekst źródłaShahid, Khadija, Saira Shahzadi i Saqib Ali. "Synthesis, coordination and biological aspects of organotin(IV) derivatives of 4-[(2,4-dinitrophenyl)amino)]-4-oxo-2-butenoic acid and 2-{[(2,4-dinitrophenyl)amino]carbonyl}benzoic acid". Journal of the Serbian Chemical Society 74, nr 2 (2009): 141–54. http://dx.doi.org/10.2298/jsc0902141s.
Pełny tekst źródłaSaid, Musa A., C. Hemavathi, S. Nagabrahmanandachari, K. C. Kumara Swamy, Damodara M. Poojary i A. Clearfield. "Syntheses and structures of new mono and multinuclear organotin phosphinates". Proceedings / Indian Academy of Sciences 108, nr 3 (czerwiec 1996): 298. http://dx.doi.org/10.1007/bf02870065.
Pełny tekst źródłaSabiha Khanam, Sabiha Khanam, Khadija Shahid Khadija Shahid, Muhammad Sirajuddin Muhammad Sirajuddin i Saqib Ali and Hameed Ullah Saqib Ali and Hameed Ullah. "Synthesis, Spectral Characterization and Biological Evaluation of Organotin(IV) Complexes of Aniline Derivatives of Naturally Occurring Betulinic Acid". Journal of the chemical society of pakistan 41, nr 4 (2019): 725. http://dx.doi.org/10.52568/000785/jcsp/41.04.2019.
Pełny tekst źródłaShariatinia, Zahra, Ebadullah Asadi, Vahid Tavasolinasab i Khodayar Gholivand. "Nanoparticles of novel organotin(IV) complexes bearing phosphoric triamide ligands". Beilstein Journal of Nanotechnology 4 (12.02.2013): 94–102. http://dx.doi.org/10.3762/bjnano.4.11.
Pełny tekst źródłaHussain, Shabbir, Saqib Ali, Saira Shahzadi, Muhammad Nawaz Tahir, Muhammad Shahid, Khurram Shahzad Munawar i Syed Mustansar Abbas. "Synthesis, spectroscopy, single crystal XRD and biological studies of multinuclear organotin dicarboxylates". Polyhedron 117 (październik 2016): 64–72. http://dx.doi.org/10.1016/j.poly.2016.05.045.
Pełny tekst źródłaDa Silva Santos, Ane Francielly, i José Roberto Da Silveira Maia. "ANTIMICROBIAL EFFECT OF ORGANOTIN COMPOUNDS DERIVED FROM PHENOLIC SCHIFF BASES". Journal of Engineering and Exact Sciences 5, nr 5 (20.12.2019): 0452–59. http://dx.doi.org/10.18540/jcecvl5iss5pp0452-0459.
Pełny tekst źródłaChagas, Rafael César Russo, José Roberto da Silveira Maia i Vany P. Ferraz. "Synthesis and characterisation of organotin(IV) derivatives of ambidentate ligands containing nitrogen and sulphur donor atoms". Main Group Metal Chemistry 34, nr 5-6 (1.12.2011): 131–37. http://dx.doi.org/10.1515/mgmc-2012-0904.
Pełny tekst źródłaYusof, Enis Nadia Md, Muhammad A. M. Latif, Mohamed I. M. Tahir, Jennette A. Sakoff, Michela I. Simone, Alister J. Page, Abhi Veerakumarasivam, Edward R. T. Tiekink i Thahira B. S. A. Ravoof. "o-Vanillin Derived Schiff Bases and Their Organotin(IV) Compounds: Synthesis, Structural Characterisation, In-Silico Studies and Cytotoxicity". International Journal of Molecular Sciences 20, nr 4 (15.02.2019): 854. http://dx.doi.org/10.3390/ijms20040854.
Pełny tekst źródłaDiallo, Waly, Libasse Diop, Cheikh Abdoul Khadir Diop, Hélène Cattey i Laurent Plasseraud. "Synthesis, spectroscopic study, and crystal structure of a new organotin(IV) selenate derivative". Main Group Metal Chemistry 41, nr 5-6 (27.11.2018): 183–88. http://dx.doi.org/10.1515/mgmc-2018-0029.
Pełny tekst źródłaIftikhar, Syed, Syeda Gilani, Babar Taj, Ahmad Raheel, U. Ud-Din-Imtiaz, Syed Termizi, Mundher Al-Shakban i Hapipah Ali. "Design, synthesis and biological evaluation of organotin(IV) complexes of flumequine and cetirizine". Journal of the Serbian Chemical Society 83, nr 4 (2018): 425–37. http://dx.doi.org/10.2298/jsc161203070i.
Pełny tekst źródłaHowell, GN, MJ Oconnor, AM Bond, HA Hudson, PJ Hanna i S. Strother. "Methylmercury Generation in Seawater by Transmethylation Reactions of Organolead and Organotin Compounds With Inorganic Mercury as Monitored by Multinuclear Magnetic-Resonance and Electrochemical Techniques". Australian Journal of Chemistry 39, nr 8 (1986): 1167. http://dx.doi.org/10.1071/ch9861167.
Pełny tekst źródłaSingh, Har Lal, i J. B. Singh. "Synthesis and Characterization of New Lead(II) and Organotin(IV) Complexes of Schiff Bases Derived from Histidine and Methionine". International Journal of Inorganic Chemistry 2012 (8.02.2012): 1–7. http://dx.doi.org/10.1155/2012/568797.
Pełny tekst źródłaDanish, Muhammad, Saqib Ali, Muhammad Mazhar, Amin Badshah, M. Iqbal Choudhary, Helmut G. Alt i Gerald Kehr. "Mössbauer, multinuclear magnetic resonance and mass spectrometric studies of organotin carboxylates of m-methyltrans-cinnamic acid". Polyhedron 14, nr 20-21 (wrzesień 1995): 3115–23. http://dx.doi.org/10.1016/0277-5387(95)00080-c.
Pełny tekst źródłaNath, Mala, Hitendra Singh, George Eng i Xueqing Song. "Interaction of 5′-Guanosine Monophosphate with Organotin(IV) Moieties: Synthesis, Structural Characterization, and Anti-Inflammatory Activity". ISRN Organic Chemistry 2012 (9.12.2012): 1–9. http://dx.doi.org/10.5402/2012/873035.
Pełny tekst źródłaPantelic, Nebojsa, Martina Lerbs, Katharina Wolf, Ludger Wessjohann i Goran Kaludjerovic. "In vitro anticancer evaluation of novel triphenyltin(IV) compounds with some N-acetyl-S-naphthoquinonylcysteine derivatives". Journal of the Serbian Chemical Society 84, nr 10 (2019): 1119–27. http://dx.doi.org/10.2298/jsc190322032p.
Pełny tekst źródłaGarcía y García, Patricia, María del Carmen Pérez-Redondo, Perla Román-Bravo, Miguel-Angel Reyes-González, Irma Linzaga-Elizalde, Marcela López-Cardoso, Patricia Martínez-Salas, Gabriela Vargas-Pineda, Ave María Cotero-Villegas i Raymundo Cea-Olivares. "Synthesis, multinuclear (1H, 13C, 31P, 119Sn) NMR and structure of new optically active organotin(IV). O,O'-di-(−)-menthyldithiophosphates". Main Group Chemistry 11, nr 2 (2012): 165–74. http://dx.doi.org/10.3233/mgc-2012-0070.
Pełny tekst źródłaWillem, Rudolph, Monique Biesemans, Pascale Jaumier i Bernard Jousseaume. "Comparative assessment of weak intramolecular coordinations at tin in functionalized mono-organotin trichlorides and mono-organotrialkynyltins by multinuclear solution NMR". Journal of Organometallic Chemistry 572, nr 2 (styczeń 1999): 233–38. http://dx.doi.org/10.1016/s0022-328x(98)00944-9.
Pełny tekst źródłaParveen, Bushra, Iftikhar Bukhari, Saira Shahzadi, Saqib Ali, Shabbir Hussain, Kulsoom Ali i Muhammad Shahid. "Synthesis and spectroscopic characterization of mononuclear/binuclear organotin(IV) complexes with 1H-1,2,4-triazole-3-thiol: Comparative studies of their antibacterial/antifungal potencies". Journal of the Serbian Chemical Society 80, nr 6 (2015): 755–66. http://dx.doi.org/10.2298/jsc140711010p.
Pełny tekst źródłaDebnath, Pratima, Paresh Debnath, Manojit Roy, Lesław Sieroń, Waldemar Maniukiewicz, Tamanna Aktar, Debasish Maiti, Alexander S. Novikov i Tarun Kumar Misra. "Novel Organotin(IV) Complexes of 2-[4-Hydroxy-3-((2-hydroxyethylimino)methyl)phenylazo]benzoic Acid: Synthesis, Structure, Noncovalent Interactions and In Vitro Antibacterial Activity". Crystals 12, nr 11 (7.11.2022): 1582. http://dx.doi.org/10.3390/cryst12111582.
Pełny tekst źródłaSadiq-ur-Rehman, Saqib Ali i Saira Shahzadi. "Organotin(IV) esters of (E)-3-furanyl-2-phenyl-2-propenoic acid: Synthesis, investigation of the coordination modes by IR, multinuclear NMR (1H,13C,119Sn) and In Vitro biological studies". Heteroatom Chemistry 19, nr 6 (wrzesień 2008): 612–20. http://dx.doi.org/10.1002/hc.20488.
Pełny tekst źródłaEndo, Kohei, Mika Ogawa i Takanori Shibata. "Multinuclear Catalyst for Copper-Catalyzed Asymmetric Conjugate Addition of Organozinc Reagents". Angewandte Chemie International Edition 49, nr 13 (23.02.2010): 2410–13. http://dx.doi.org/10.1002/anie.200906839.
Pełny tekst źródłaEndo, Kohei, Mika Ogawa i Takanori Shibata. "Multinuclear Catalyst for Copper-Catalyzed Asymmetric Conjugate Addition of Organozinc Reagents". Angewandte Chemie 122, nr 13 (23.02.2010): 2460–63. http://dx.doi.org/10.1002/ange.200906839.
Pełny tekst źródłaEndo, Kohei, Mika Ogawa i Takanori Shibata. "ChemInform Abstract: Multinuclear Catalyst for Copper-Catalyzed Asymmetric Conjugate Addition of Organozinc Reagents." ChemInform 41, nr 32 (23.07.2010): no. http://dx.doi.org/10.1002/chin.201032086.
Pełny tekst źródłaEndo, Kohei, Daisuke Hamada, Sayuri Yakeishi, Mika Ogawa i Takanori Shibata. "Multinuclear Cu-Catalysts Based on SPINOL-PHOS in Asymmetric Conjugate Addition of Organozinc Reagents". Organic Letters 14, nr 9 (20.04.2012): 2342–45. http://dx.doi.org/10.1021/ol300748d.
Pełny tekst źródłaEndo, Kohei, Sayuri Yakeishi, Daisuke Hamada i Takanori Shibata. "Functionalized BINOL-mono-PHOS for Multinuclear Cu-Catalysts in Asymmetric Conjugate Addition of Organozinc Reagents". Chemistry Letters 42, nr 5 (5.05.2013): 547–49. http://dx.doi.org/10.1246/cl.130080.
Pełny tekst źródłaEndo, Kohei, Daisuke Hamada, Sayuri Yakeishi, Mika Ogawa i Takanori Shibata. "ChemInform Abstract: Multinuclear Cu-Catalysts Based on SPINOL-PHOS in Asymmetric Conjugate Addition of Organozinc Reagents." ChemInform 43, nr 34 (26.07.2012): no. http://dx.doi.org/10.1002/chin.201234062.
Pełny tekst źródłaEndo, Kohei, Takanori Shibata i Ryotaro Takayama. "BINAM-mono-PHOS as New Entry for Multinuclear Copper Catalysts in Asymmetric Conjugate Addition of Organozinc Reagents". Synlett 24, nr 09 (23.04.2013): 1155–59. http://dx.doi.org/10.1055/s-0033-1338439.
Pełny tekst źródłaEndo, Kohei, Sayuri Yakeishi, Daisuke Hamada i Takanori Shibata. "ChemInform Abstract: Functionalized BINOL-mono-PHOS for Multinuclear Cu-Catalysts in Asymmetric Conjugate Addition of Organozinc Reagents." ChemInform 45, nr 46 (30.10.2014): no. http://dx.doi.org/10.1002/chin.201446105.
Pełny tekst źródłaEndo, Kohei, Ryotaro Takayama i Takanori Shibata. "ChemInform Abstract: BINAM-mono-PHOS as New Entry for Multinuclear Copper Catalysts in Asymmetric Conjugate Addition of Organozinc Reagents." ChemInform 44, nr 39 (5.09.2013): no. http://dx.doi.org/10.1002/chin.201339070.
Pełny tekst źródłaRibot, François O., Delphine Minoux i Clément Sanchez. "An Organotin Oxo-Carboxylate Cluster Functionalized by Triethoxysilyl Groups". MRS Proceedings 628 (2000). http://dx.doi.org/10.1557/proc-628-cc2.2.
Pełny tekst źródłaJiang, Wujiu, Zhijian Zhang, Penghui Ni i Yuxing Tan. "Self-assembly synthesis of diorganotin complexes base on arylformylhydrazone possessing ONO donor set: anticancer activity and mechanism". Metallomics, 30.03.2022. http://dx.doi.org/10.1093/mtomcs/mfac021.
Pełny tekst źródłaKHOSA, MUHAMMAD KALEEM, MUHAMMAD MAZHAR, SAQIB ALI i SARIM DASTGIR. "Synthesis, characterisation, and structural elucidation by spectral investigation (FT-IR, multinuclear NMR, mass spectrometry) of biologically active organotin(IV) compounds containing germanium". Turkish Journal of Chemistry, 1.01.2010. http://dx.doi.org/10.3906/kim-0904-10.
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