Artículos de revistas sobre el tema "Thiocarbonyl Group"
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Kirby, Christopher W., Michael D. Lumsden y Roderick E. Wasylishen. "A solid-state 13C NMR and theoretical investigation of carbonyl and thiocarbonyl carbon chemical shift tensors". Canadian Journal of Chemistry 73, n.º 4 (1 de abril de 1995): 604–13. http://dx.doi.org/10.1139/v95-078.
Texto completoMOLINA, M. T., M. YANEZ, O. MO, R. NOTARIO y J. L. M. ABBOUD. "ChemInform Abstract: The Thiocarbonyl Group". ChemInform 29, n.º 13 (23 de junio de 2010): no. http://dx.doi.org/10.1002/chin.199813281.
Texto completoFernandez, José Manuel García y Carmen Ortiz Mellet. "The Thiocarbonyl Group in Carbohydrate Chemistry". Sulfur reports 19, n.º 1 (septiembre de 1996): 61–159. http://dx.doi.org/10.1080/01961779608047905.
Texto completoCorsaro, Antonino y Venerando Pistarà. "Conversion of the thiocarbonyl group into the carbonyl group". Tetrahedron 54, n.º 50 (diciembre de 1998): 15027–62. http://dx.doi.org/10.1016/s0040-4020(98)00880-1.
Texto completoCrich, David y Leticia Quintero. "Radical chemistry associated with the thiocarbonyl group". Chemical Reviews 89, n.º 7 (noviembre de 1989): 1413–32. http://dx.doi.org/10.1021/cr00097a001.
Texto completoKook Sohn, Chang, Eun Kyung Ma, Chang Kon Kim, Hai Whang Lee y Ikchoon Lee. "Theoretical studies on thiocarbonyl group transfer reactions". New Journal of Chemistry 25, n.º 6 (2001): 859–63. http://dx.doi.org/10.1039/b010202o.
Texto completoHuang, Chun-Hao, Pei-Jhen Wu, Kun-You Chung, Yi-An Chen, Elise Y. Li y Pi-Tai Chou. "Room-temperature phosphorescence from small organic systems containing a thiocarbonyl moiety". Physical Chemistry Chemical Physics 19, n.º 13 (2017): 8896–901. http://dx.doi.org/10.1039/c7cp00074j.
Texto completoAbram, Ulrich y Bernd Lorenz. "Thiocarbonyl Complexes of Rhenium. Part I." Zeitschrift für Naturforschung B 48, n.º 6 (1 de junio de 1993): 771–77. http://dx.doi.org/10.1515/znb-1993-0611.
Texto completoBarton, Derek H. R., Peter I. Dalko y Stephan D. Géro. "Radical cation reactions associated with the thiocarbonyl group". Tetrahedron Letters 33, n.º 14 (marzo de 1992): 1883–86. http://dx.doi.org/10.1016/s0040-4039(00)74167-0.
Texto completoGARCIA FERNANDEZ, J. M. y C. ORTIZ MELLET. "ChemInform Abstract: The Thiocarbonyl Group in Carbohydrate Chemistry". ChemInform 28, n.º 28 (3 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199728234.
Texto completoGouran, Ali Asghar y Sakineh Asghari. "On Searching for a Stepwise Channel for the Mechanism of a 1,3-Dipolar Cycloaddition between a Thiocarbonyl S-Oxide and C20 Fullerene using Born–Oppenheimer ab Initio QM/MM Molecular Dynamics". Progress in Reaction Kinetics and Mechanism 42, n.º 3 (septiembre de 2017): 282–88. http://dx.doi.org/10.3184/146867817x14954764850315.
Texto completoCorsaro, Antonio y Venerando Pistara. "ChemInform Abstract: Conversion of the Thiocarbonyl Group into the Carbonyl Group". ChemInform 30, n.º 17 (16 de junio de 2010): no. http://dx.doi.org/10.1002/chin.199917302.
Texto completoZhang, Zhong, Qian-shu Li, Yaoming Xie, R. Bruce King y Henry F. Schaefer. "Iron Carbonyl Thiocarbonyls: Effect of Substituting a Thiocarbonyl Group for a Carbonyl Group in Mononuclear and Binuclear Iron Carbonyl Derivatives". Inorganic Chemistry 48, n.º 5 (2 de marzo de 2009): 1974–88. http://dx.doi.org/10.1021/ic8016276.
Texto completoReepmeyer, John C. y D. Andr d'Avignon. "Use of a Hydrolytic Procedure and Spectrometric Methods in the Structure Elucidation of a Thiocarbonyl Analogue of Sildenafil Detected as an Adulterant in an Over-the-Counter Herbal Aphrodisiac". Journal of AOAC INTERNATIONAL 92, n.º 5 (1 de septiembre de 2009): 1336–42. http://dx.doi.org/10.1093/jaoac/92.5.1336.
Texto completoNarasimhamurthy, N. y A. G. Samuelson. "Thiocarbonyl to carbonyl group transformation using CuCl and NaOH". Tetrahedron Letters 27, n.º 33 (enero de 1986): 3911–12. http://dx.doi.org/10.1016/s0040-4039(00)83914-3.
Texto completoBARTON, D. H. R., P. I. DALKO y S. D. GERO. "ChemInform Abstract: Radical Cation Reactions Associated with the Thiocarbonyl Group." ChemInform 23, n.º 41 (21 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199241068.
Texto completoTanaka, Y., K. Taguchi y H. Utsumi. "Toxicity assessment of 255 chemicals to pure cultured nitrifying bacteria using biosensor". Water Science and Technology 46, n.º 11-12 (1 de diciembre de 2002): 331–35. http://dx.doi.org/10.2166/wst.2002.0758.
Texto completoYetra, Santhivardhana Reddy, Zhigao Shen, Hui Wang y Lutz Ackermann. "Thiocarbonyl-enabled ferrocene C–H nitrogenation by cobalt(III) catalysis: thermal and mechanochemical". Beilstein Journal of Organic Chemistry 14 (25 de junio de 2018): 1546–53. http://dx.doi.org/10.3762/bjoc.14.131.
Texto completoBalyueva, Yuliya, Nina Sosnovskaya y Igor' Rozencveyg. "GLOSS-FORMING EFFECT OF TRICHLOROETHYL AMIDES WITH THIOAMIDE FUNCTIONS IN ELECTROCHEMICAL NICKEL PLATING TECHNOLOGY". Modern Technologies and Scientific and Technological Progress 2022, n.º 1 (16 de mayo de 2022): 11–12. http://dx.doi.org/10.36629/2686-9896-2022-1-11-12.
Texto completoQuiclet-Sire, Beatrice y Samir Z. Zard. "A Convenient, High Yielding Cleavage of the Thiocarbonyl Group in Xanthates". Bulletin of the Korean Chemical Society 31, n.º 3 (20 de marzo de 2010): 543–44. http://dx.doi.org/10.5012/bkcs.2010.31.03.543.
Texto completoPogorilyy, Viktor, Petr Ostroverkhov, Valeria Efimova, Ekaterina Plotnikova, Olga Bezborodova, Ekaterina Diachkova, Yuriy Vasil’ev, Andrei Pankratov y Mikhail Grin. "Thiocarbonyl Derivatives of Natural Chlorins: Synthesis Using Lawesson’s Reagent and a Study of Their Properties". Molecules 28, n.º 10 (20 de mayo de 2023): 4215. http://dx.doi.org/10.3390/molecules28104215.
Texto completoShurupov, Dmitriy, Yuliya Andreeva, Yuliya Balyueva, Nina Sosnovskaya y Igor' Rozencveyg. "PROSPECTS FOR THE USE OF TRICHLOROETHYL AMIDES WITH THIOAMIDE FUNCTIONS IN THE TECHNOLOGY OF BRILLIANT NICKEL PLATING". Modern Technologies and Scientific and Technological Progress 1, n.º 1 (17 de mayo de 2021): 101–2. http://dx.doi.org/10.36629/2686-9896-2021-1-1-101-102.
Texto completoYamada, Shinji, Tomoko Misono y Seiji Tsuzuki. "Cation−π Interactions of a Thiocarbonyl Group and a Carbonyl Group with a Pyridinium Nucleus". Journal of the American Chemical Society 126, n.º 31 (agosto de 2004): 9862–72. http://dx.doi.org/10.1021/ja0490119.
Texto completoSereda, Oksana, Nicole Clemens, Tatjana Heckel y René Wilhelm. "Imidazolinium and amidinium salts as Lewis acid organocatalysts". Beilstein Journal of Organic Chemistry 8 (18 de octubre de 2012): 1798–803. http://dx.doi.org/10.3762/bjoc.8.205.
Texto completoNakayama, Juzo, Taku Kitahara, Yoshiaki Sugihara y Akihiko Ishii. "Ambident Reactivities of Carbenium Salts Possessing a Thiocarbonyl Group at theβ-Position". Chemistry Letters 28, n.º 2 (febrero de 1999): 187–88. http://dx.doi.org/10.1246/cl.1999.187.
Texto completoYamada, Shinji y Tomoko Misono. "Intra- and intermolecular interactions between a thiocarbonyl group and a pyridinium nucleus". Tetrahedron Letters 42, n.º 32 (agosto de 2001): 5497–500. http://dx.doi.org/10.1016/s0040-4039(01)01066-8.
Texto completoSugimoto, Toyonari, Yukishi Yamamoto y Zen-ichi Yoshida. "Synthesis and Electrical Conductive Property of New Tellurium Polymers Containing Thiocarbonyl Group". Chemistry Letters 19, n.º 11 (noviembre de 1990): 2111–14. http://dx.doi.org/10.1246/cl.1990.2111.
Texto completoPetz, Wolfgang y Frank Weller. "Thiocarbonylkomplexe des Eisens, VII [1] / Thiocarbonyl Complexes of Iron, VII [1]". Zeitschrift für Naturforschung B 46, n.º 8 (1 de agosto de 1991): 971–77. http://dx.doi.org/10.1515/znb-1991-0801.
Texto completoMohammadpoor-Baltork, Iraj, Majid M. M. Sadeghi y Karim Esmayilpour. "Convenient transformation of thiocarbonyl to carbonyl group using benzyltriphenylphosphonium and n-butyltriphenylphosphonium peroxodisulfates". Journal of Chemical Research 2003, n.º 6 (1 de junio de 2003): 348–50. http://dx.doi.org/10.3184/030823403103174074.
Texto completoQuiclet-Sire, Beatrice y Samir Z. Zard. "ChemInform Abstract: A Convenient, High Yielding Cleavage of the Thiocarbonyl Group in Xanthates." ChemInform 41, n.º 30 (1 de julio de 2010): no. http://dx.doi.org/10.1002/chin.201030036.
Texto completoKinemuchi, Haruki y Bungo Ochiai. "Synthesis of Hydrophilic Sulfur-Containing Adsorbents for Noble Metals Having Thiocarbonyl Group Based on a Methacrylate Bearing Dithiocarbonate Moieties". Advances in Materials Science and Engineering 2018 (2018): 1–8. http://dx.doi.org/10.1155/2018/3729580.
Texto completoKiran, Kuppalli R., Toreshettahally R. Swaroop, Kodipura P. Sukrutha, Jeegundipattana B. Shruthi, Seegehally M. Anil, Kanchugarakoppal S. Rangappa y Maralinganadoddi P. Sadashiva. "Acid-Catalyzed Condensation of o-Phenylenediammines and o-Aminophenols with α-Oxodithioesters: A Divergent and Regioselective Synthesis of 2-Methylthio-3-aryl/Heteroarylquinoxalines and 2-Acylbenzoxazoles". Synthesis 51, n.º 22 (23 de septiembre de 2019): 4205–14. http://dx.doi.org/10.1055/s-0039-1690616.
Texto completoMasuda, Ryōichi, Masaru Hojo, Tadaaki Ichi, Shigetoshi Sasano, Tatsuya Kobayashi y Chihiro Kuroda. "An alternative efficient method for transformation of thiocarbonyl to carbonyl group using trifluoroacetic anhydride". Tetrahedron Letters 32, n.º 9 (febrero de 1991): 1195–98. http://dx.doi.org/10.1016/s0040-4039(00)92042-2.
Texto completoBarnabas, Mary V., Krishnan Venkateswaran y David C. Walker. "Comparison of muonium and positronium with hydrogen atoms in their reactions towards solutes containing amide and peptide linkages in water and micelle solutions". Canadian Journal of Chemistry 67, n.º 1 (1 de enero de 1989): 120–26. http://dx.doi.org/10.1139/v89-020.
Texto completoSeidelmann, Oliver, Lothar Beyer y Rainer Richter. "N,N-Disubstituierte Nʹ-Ferrocenoylthioharnstoffe als zweizähnige Komplexliganden für Übergangsmetallionen. Kristallstruktur von Bis-(N,N-diethyl-Nʹ-ferrocenoylthioureato)nickel(II) / N,N-Disubstituted Nʹ-Ferrocenoyl Thioureas as Bidentate Ligands for Transition Metal Ions. Crystal Structure of Bis-(N,N-diethyl-Nʹ-ferrocenoylthioureato)nickel(II)". Zeitschrift für Naturforschung B 50, n.º 11 (1 de noviembre de 1995): 1679–84. http://dx.doi.org/10.1515/znb-1995-1115.
Texto completoBabashkina, Maria G. y Damir A. Safin. "Zn(II), Co(II) and Ni(II) complexes of a phosphorylthiourea derivative of 4-[(EtO)2P(O)CH2]-C6H4-NHC(S)NHP(O)(OiPr)2". Collection of Czechoslovak Chemical Communications 75, n.º 5 (2010): 507–15. http://dx.doi.org/10.1135/cccc2009074.
Texto completoSelvakumar, N., Mohammed A. Raheem, Manoj Kumar Khera, Trideep V. Rajale, Magadi Sitaram Kumar, Sreenivas Kandepu, Jagattaran Das, R. Rajagopalan, Javed Iqbal y Sanjay Trehan. "Influence of ethylene-Oxy spacer group on the activity of linezolid: Synthesis of potent antibacterials possessing a thiocarbonyl group". Bioorganic & Medicinal Chemistry Letters 13, n.º 23 (diciembre de 2003): 4169–72. http://dx.doi.org/10.1016/j.bmcl.2003.08.068.
Texto completoElhady, Omar M., Erian S. Mansour, M. M. Elwassimy, Sameh A. Zawam y Ali M. Drar. "Synthesis and characterization of some new tebufenozide analogues and study their toxicological effect against Spodoptera littoralis (Boisd.)". Current Chemistry Letters 11, n.º 1 (2022): 63–68. http://dx.doi.org/10.5267/j.ccl.2021.9.005.
Texto completoNakayama, Juzo, Taku Kitahara, Yoshiaki Sugihara y Akihiko Ishii. "ChemInform Abstract: Ambident Reactivities of Carbenium Salts Possessing a Thiocarbonyl Group at the β-Position." ChemInform 30, n.º 27 (15 de junio de 2010): no. http://dx.doi.org/10.1002/chin.199927147.
Texto completoCaracelli, Ignez, Paulo R. Olivato, Henrique J. Traesel, Jéssica Valença, Daniel N. S. Rodrigues y Edward R. T. Tiekink. "Crystal structure of 2-methoxy-2-[(4-methoxyphenyl)sulfanyl]-1-phenylethanone". Acta Crystallographica Section E Crystallographic Communications 71, n.º 9 (15 de agosto de 2015): o657—o658. http://dx.doi.org/10.1107/s2056989015014565.
Texto completoKetcham, Roger, Ernst Schaumann y Gunadi Adiwidjaja. "The Reaction of Cyanothioformamide with Isocyanates − Formation of a Disulfide by Reduction of a Thiocarbonyl Group". European Journal of Organic Chemistry 2001, n.º 9 (mayo de 2001): 1695–99. http://dx.doi.org/10.1002/1099-0690(200105)2001:9<1695::aid-ejoc1695>3.0.co;2-0.
Texto completoBARLUENGA, J., E. RUBIO y M. TOMAS. "ChemInform Abstract: Functions Containing a Thiocarbonyl Group Bearing Two Heteroatoms Other than a Halogen or Chalcogen". ChemInform 27, n.º 35 (5 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199635271.
Texto completoMASUDA, R., M. HOJO, T. ICHI, S. SASANO, T. KOBAYASHI y C. KURODA. "ChemInform Abstract: An Alternative Efficient Method for Transformation of Thiocarbonyl to Carbonyl Group Using Trifluoroacetic Anhydride." ChemInform 22, n.º 52 (22 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199152111.
Texto completoJanssen, M. J. "Physical properties of organic thiones: Part IV. The basicity of the thiocarbonyl group in various thiones". Recueil des Travaux Chimiques des Pays-Bas 81, n.º 8 (2 de septiembre de 2010): 650–60. http://dx.doi.org/10.1002/recl.19620810803.
Texto completoEccles, Kevin, Robin Morrison, Abhijeet Sinha, Anita Maguire y Simon Lawrence. "Halogen Bonding with Sulfur Functional Groups". Acta Crystallographica Section A Foundations and Advances 70, a1 (5 de agosto de 2014): C651. http://dx.doi.org/10.1107/s2053273314093486.
Texto completoLópez-Pérez, Liliana, Hortensia Maldonado-Textle, Luis Ernesto Elizalde-Herrera, J. Guadalupe Telles-Padilla, Ramiro Guerrero-Santos, Scott Collins, Enrique Javier Jiménez-Regalado y Claude St Thomas. "Methylation of poly(acrylic acid), prepared using RAFT polymerization, with trimethylsilyldiazomethane: A metamorphosis of the thiocarbonyl group to a thiol-end group". Polymer 168 (abril de 2019): 116–25. http://dx.doi.org/10.1016/j.polymer.2019.02.025.
Texto completoLanterna, Anabel E., María F. Torresan, Rodrigo A. Iglesias, Eduardo A. Coronado y Alejandro M. Granados. "Remarkable effect of the dithiafulvene structures on their capacity as reducing agents: Influence of conjugated thiocarbonyl group". Applied Surface Science 465 (enero de 2019): 1061–65. http://dx.doi.org/10.1016/j.apsusc.2018.09.243.
Texto completoSakamoto, Masami, Hiroya Kawanishi, Takashi Mino y Tsutomu Fujita. "Asymmetric synthesis of β-lactams using chiral-memory effect on photochemical γ-hydrogen abstraction by thiocarbonyl group". Chemical Communications, n.º 18 (2008): 2132. http://dx.doi.org/10.1039/b801524d.
Texto completoMereshchenko, Andrey S., Alexey V. Ivanov, Viktor I. Baranovskii, Grzegorz Mloston, Ludmila L. Rodina y Valerij A. Nikolaev. "On the strong difference in reactivity of acyclic and cyclic diazodiketones with thioketones: experimental results and quantum-chemical interpretation". Beilstein Journal of Organic Chemistry 11 (20 de abril de 2015): 504–13. http://dx.doi.org/10.3762/bjoc.11.57.
Texto completoColeman, Robert S. y James M. Siedlecki. "Synthesis of a 4-thio-2'-deoxyuridine containing oligonucleotide. Development of the thiocarbonyl group as a linker element." Journal of the American Chemical Society 114, n.º 23 (noviembre de 1992): 9229–30. http://dx.doi.org/10.1021/ja00049a089.
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