Статті в журналах з теми "Thiocarbonyl Group"
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Kirby, Christopher W., Michael D. Lumsden, and Roderick E. Wasylishen. "A solid-state 13C NMR and theoretical investigation of carbonyl and thiocarbonyl carbon chemical shift tensors." Canadian Journal of Chemistry 73, no. 4 (April 1, 1995): 604–13. http://dx.doi.org/10.1139/v95-078.
Повний текст джерелаMOLINA, M. T., M. YANEZ, O. MO, R. NOTARIO, and J. L. M. ABBOUD. "ChemInform Abstract: The Thiocarbonyl Group." ChemInform 29, no. 13 (June 23, 2010): no. http://dx.doi.org/10.1002/chin.199813281.
Повний текст джерелаFernandez, José Manuel García, and Carmen Ortiz Mellet. "The Thiocarbonyl Group in Carbohydrate Chemistry." Sulfur reports 19, no. 1 (September 1996): 61–159. http://dx.doi.org/10.1080/01961779608047905.
Повний текст джерелаCorsaro, Antonino, and Venerando Pistarà. "Conversion of the thiocarbonyl group into the carbonyl group." Tetrahedron 54, no. 50 (December 1998): 15027–62. http://dx.doi.org/10.1016/s0040-4020(98)00880-1.
Повний текст джерелаCrich, David, and Leticia Quintero. "Radical chemistry associated with the thiocarbonyl group." Chemical Reviews 89, no. 7 (November 1989): 1413–32. http://dx.doi.org/10.1021/cr00097a001.
Повний текст джерелаKook Sohn, Chang, Eun Kyung Ma, Chang Kon Kim, Hai Whang Lee, and Ikchoon Lee. "Theoretical studies on thiocarbonyl group transfer reactions." New Journal of Chemistry 25, no. 6 (2001): 859–63. http://dx.doi.org/10.1039/b010202o.
Повний текст джерелаHuang, Chun-Hao, Pei-Jhen Wu, Kun-You Chung, Yi-An Chen, Elise Y. Li, and Pi-Tai Chou. "Room-temperature phosphorescence from small organic systems containing a thiocarbonyl moiety." Physical Chemistry Chemical Physics 19, no. 13 (2017): 8896–901. http://dx.doi.org/10.1039/c7cp00074j.
Повний текст джерелаAbram, Ulrich, and Bernd Lorenz. "Thiocarbonyl Complexes of Rhenium. Part I." Zeitschrift für Naturforschung B 48, no. 6 (June 1, 1993): 771–77. http://dx.doi.org/10.1515/znb-1993-0611.
Повний текст джерелаBarton, Derek H. R., Peter I. Dalko, and Stephan D. Géro. "Radical cation reactions associated with the thiocarbonyl group." Tetrahedron Letters 33, no. 14 (March 1992): 1883–86. http://dx.doi.org/10.1016/s0040-4039(00)74167-0.
Повний текст джерелаGARCIA FERNANDEZ, J. M., and C. ORTIZ MELLET. "ChemInform Abstract: The Thiocarbonyl Group in Carbohydrate Chemistry." ChemInform 28, no. 28 (August 3, 2010): no. http://dx.doi.org/10.1002/chin.199728234.
Повний текст джерелаGouran, Ali Asghar, and 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, no. 3 (September 2017): 282–88. http://dx.doi.org/10.3184/146867817x14954764850315.
Повний текст джерелаCorsaro, Antonio, and Venerando Pistara. "ChemInform Abstract: Conversion of the Thiocarbonyl Group into the Carbonyl Group." ChemInform 30, no. 17 (June 16, 2010): no. http://dx.doi.org/10.1002/chin.199917302.
Повний текст джерелаZhang, Zhong, Qian-shu Li, Yaoming Xie, R. Bruce King, and 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, no. 5 (March 2, 2009): 1974–88. http://dx.doi.org/10.1021/ic8016276.
Повний текст джерелаReepmeyer, John C., and 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, no. 5 (September 1, 2009): 1336–42. http://dx.doi.org/10.1093/jaoac/92.5.1336.
Повний текст джерелаNarasimhamurthy, N., and A. G. Samuelson. "Thiocarbonyl to carbonyl group transformation using CuCl and NaOH." Tetrahedron Letters 27, no. 33 (January 1986): 3911–12. http://dx.doi.org/10.1016/s0040-4039(00)83914-3.
Повний текст джерелаBARTON, D. H. R., P. I. DALKO, and S. D. GERO. "ChemInform Abstract: Radical Cation Reactions Associated with the Thiocarbonyl Group." ChemInform 23, no. 41 (August 21, 2010): no. http://dx.doi.org/10.1002/chin.199241068.
Повний текст джерелаTanaka, Y., K. Taguchi, and H. Utsumi. "Toxicity assessment of 255 chemicals to pure cultured nitrifying bacteria using biosensor." Water Science and Technology 46, no. 11-12 (December 1, 2002): 331–35. http://dx.doi.org/10.2166/wst.2002.0758.
Повний текст джерелаYetra, Santhivardhana Reddy, Zhigao Shen, Hui Wang, and Lutz Ackermann. "Thiocarbonyl-enabled ferrocene C–H nitrogenation by cobalt(III) catalysis: thermal and mechanochemical." Beilstein Journal of Organic Chemistry 14 (June 25, 2018): 1546–53. http://dx.doi.org/10.3762/bjoc.14.131.
Повний текст джерелаBalyueva, Yuliya, Nina Sosnovskaya, and Igor' Rozencveyg. "GLOSS-FORMING EFFECT OF TRICHLOROETHYL AMIDES WITH THIOAMIDE FUNCTIONS IN ELECTROCHEMICAL NICKEL PLATING TECHNOLOGY." Modern Technologies and Scientific and Technological Progress 2022, no. 1 (May 16, 2022): 11–12. http://dx.doi.org/10.36629/2686-9896-2022-1-11-12.
Повний текст джерелаQuiclet-Sire, Beatrice, and Samir Z. Zard. "A Convenient, High Yielding Cleavage of the Thiocarbonyl Group in Xanthates." Bulletin of the Korean Chemical Society 31, no. 3 (March 20, 2010): 543–44. http://dx.doi.org/10.5012/bkcs.2010.31.03.543.
Повний текст джерелаPogorilyy, Viktor, Petr Ostroverkhov, Valeria Efimova, Ekaterina Plotnikova, Olga Bezborodova, Ekaterina Diachkova, Yuriy Vasil’ev, Andrei Pankratov, and Mikhail Grin. "Thiocarbonyl Derivatives of Natural Chlorins: Synthesis Using Lawesson’s Reagent and a Study of Their Properties." Molecules 28, no. 10 (May 20, 2023): 4215. http://dx.doi.org/10.3390/molecules28104215.
Повний текст джерелаShurupov, Dmitriy, Yuliya Andreeva, Yuliya Balyueva, Nina Sosnovskaya, and 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, no. 1 (May 17, 2021): 101–2. http://dx.doi.org/10.36629/2686-9896-2021-1-1-101-102.
Повний текст джерелаYamada, Shinji, Tomoko Misono та Seiji Tsuzuki. "Cation−π Interactions of a Thiocarbonyl Group and a Carbonyl Group with a Pyridinium Nucleus". Journal of the American Chemical Society 126, № 31 (серпень 2004): 9862–72. http://dx.doi.org/10.1021/ja0490119.
Повний текст джерелаSereda, Oksana, Nicole Clemens, Tatjana Heckel, and René Wilhelm. "Imidazolinium and amidinium salts as Lewis acid organocatalysts." Beilstein Journal of Organic Chemistry 8 (October 18, 2012): 1798–803. http://dx.doi.org/10.3762/bjoc.8.205.
Повний текст джерелаNakayama, Juzo, Taku Kitahara, Yoshiaki Sugihara та Akihiko Ishii. "Ambident Reactivities of Carbenium Salts Possessing a Thiocarbonyl Group at theβ-Position". Chemistry Letters 28, № 2 (лютий 1999): 187–88. http://dx.doi.org/10.1246/cl.1999.187.
Повний текст джерелаYamada, Shinji, and Tomoko Misono. "Intra- and intermolecular interactions between a thiocarbonyl group and a pyridinium nucleus." Tetrahedron Letters 42, no. 32 (August 2001): 5497–500. http://dx.doi.org/10.1016/s0040-4039(01)01066-8.
Повний текст джерелаSugimoto, Toyonari, Yukishi Yamamoto, and Zen-ichi Yoshida. "Synthesis and Electrical Conductive Property of New Tellurium Polymers Containing Thiocarbonyl Group." Chemistry Letters 19, no. 11 (November 1990): 2111–14. http://dx.doi.org/10.1246/cl.1990.2111.
Повний текст джерелаPetz, Wolfgang, and Frank Weller. "Thiocarbonylkomplexe des Eisens, VII [1] / Thiocarbonyl Complexes of Iron, VII [1]." Zeitschrift für Naturforschung B 46, no. 8 (August 1, 1991): 971–77. http://dx.doi.org/10.1515/znb-1991-0801.
Повний текст джерелаMohammadpoor-Baltork, Iraj, Majid M. M. Sadeghi, and Karim Esmayilpour. "Convenient transformation of thiocarbonyl to carbonyl group using benzyltriphenylphosphonium and n-butyltriphenylphosphonium peroxodisulfates." Journal of Chemical Research 2003, no. 6 (June 1, 2003): 348–50. http://dx.doi.org/10.3184/030823403103174074.
Повний текст джерелаQuiclet-Sire, Beatrice, and Samir Z. Zard. "ChemInform Abstract: A Convenient, High Yielding Cleavage of the Thiocarbonyl Group in Xanthates." ChemInform 41, no. 30 (July 1, 2010): no. http://dx.doi.org/10.1002/chin.201030036.
Повний текст джерелаKinemuchi, Haruki, and 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.
Повний текст джерелаKiran, Kuppalli R., Toreshettahally R. Swaroop, Kodipura P. Sukrutha, Jeegundipattana B. Shruthi, Seegehally M. Anil, Kanchugarakoppal S. Rangappa та 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, № 22 (23 вересня 2019): 4205–14. http://dx.doi.org/10.1055/s-0039-1690616.
Повний текст джерелаMasuda, Ryōichi, Masaru Hojo, Tadaaki Ichi, Shigetoshi Sasano, Tatsuya Kobayashi, and Chihiro Kuroda. "An alternative efficient method for transformation of thiocarbonyl to carbonyl group using trifluoroacetic anhydride." Tetrahedron Letters 32, no. 9 (February 1991): 1195–98. http://dx.doi.org/10.1016/s0040-4039(00)92042-2.
Повний текст джерелаBarnabas, Mary V., Krishnan Venkateswaran, and 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, no. 1 (January 1, 1989): 120–26. http://dx.doi.org/10.1139/v89-020.
Повний текст джерелаSeidelmann, Oliver, Lothar Beyer та 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, № 11 (1 листопада 1995): 1679–84. http://dx.doi.org/10.1515/znb-1995-1115.
Повний текст джерелаBabashkina, Maria G., and 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, no. 5 (2010): 507–15. http://dx.doi.org/10.1135/cccc2009074.
Повний текст джерелаSelvakumar, N., Mohammed A. Raheem, Manoj Kumar Khera, Trideep V. Rajale, Magadi Sitaram Kumar, Sreenivas Kandepu, Jagattaran Das, R. Rajagopalan, Javed Iqbal, and 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, no. 23 (December 2003): 4169–72. http://dx.doi.org/10.1016/j.bmcl.2003.08.068.
Повний текст джерелаElhady, Omar M., Erian S. Mansour, M. M. Elwassimy, Sameh A. Zawam, and Ali M. Drar. "Synthesis and characterization of some new tebufenozide analogues and study their toxicological effect against Spodoptera littoralis (Boisd.)." Current Chemistry Letters 11, no. 1 (2022): 63–68. http://dx.doi.org/10.5267/j.ccl.2021.9.005.
Повний текст джерелаNakayama, Juzo, Taku Kitahara, Yoshiaki Sugihara та Akihiko Ishii. "ChemInform Abstract: Ambident Reactivities of Carbenium Salts Possessing a Thiocarbonyl Group at the β-Position." ChemInform 30, № 27 (15 червня 2010): no. http://dx.doi.org/10.1002/chin.199927147.
Повний текст джерелаCaracelli, Ignez, Paulo R. Olivato, Henrique J. Traesel, Jéssica Valença, Daniel N. S. Rodrigues, and Edward R. T. Tiekink. "Crystal structure of 2-methoxy-2-[(4-methoxyphenyl)sulfanyl]-1-phenylethanone." Acta Crystallographica Section E Crystallographic Communications 71, no. 9 (August 15, 2015): o657—o658. http://dx.doi.org/10.1107/s2056989015014565.
Повний текст джерелаKetcham, Roger, Ernst Schaumann, and Gunadi Adiwidjaja. "The Reaction of Cyanothioformamide with Isocyanates − Formation of a Disulfide by Reduction of a Thiocarbonyl Group." European Journal of Organic Chemistry 2001, no. 9 (May 2001): 1695–99. http://dx.doi.org/10.1002/1099-0690(200105)2001:9<1695::aid-ejoc1695>3.0.co;2-0.
Повний текст джерелаBARLUENGA, J., E. RUBIO, and M. TOMAS. "ChemInform Abstract: Functions Containing a Thiocarbonyl Group Bearing Two Heteroatoms Other than a Halogen or Chalcogen." ChemInform 27, no. 35 (August 5, 2010): no. http://dx.doi.org/10.1002/chin.199635271.
Повний текст джерелаMASUDA, R., M. HOJO, T. ICHI, S. SASANO, T. KOBAYASHI, and C. KURODA. "ChemInform Abstract: An Alternative Efficient Method for Transformation of Thiocarbonyl to Carbonyl Group Using Trifluoroacetic Anhydride." ChemInform 22, no. 52 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199152111.
Повний текст джерелаJanssen, 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, no. 8 (September 2, 2010): 650–60. http://dx.doi.org/10.1002/recl.19620810803.
Повний текст джерелаEccles, Kevin, Robin Morrison, Abhijeet Sinha, Anita Maguire, and Simon Lawrence. "Halogen Bonding with Sulfur Functional Groups." Acta Crystallographica Section A Foundations and Advances 70, a1 (August 5, 2014): C651. http://dx.doi.org/10.1107/s2053273314093486.
Повний текст джерелаLópez-Pérez, Liliana, Hortensia Maldonado-Textle, Luis Ernesto Elizalde-Herrera, J. Guadalupe Telles-Padilla, Ramiro Guerrero-Santos, Scott Collins, Enrique Javier Jiménez-Regalado, and 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 (April 2019): 116–25. http://dx.doi.org/10.1016/j.polymer.2019.02.025.
Повний текст джерелаLanterna, Anabel E., María F. Torresan, Rodrigo A. Iglesias, Eduardo A. Coronado, and Alejandro M. Granados. "Remarkable effect of the dithiafulvene structures on their capacity as reducing agents: Influence of conjugated thiocarbonyl group." Applied Surface Science 465 (January 2019): 1061–65. http://dx.doi.org/10.1016/j.apsusc.2018.09.243.
Повний текст джерелаSakamoto, Masami, Hiroya Kawanishi, Takashi Mino та Tsutomu Fujita. "Asymmetric synthesis of β-lactams using chiral-memory effect on photochemical γ-hydrogen abstraction by thiocarbonyl group". Chemical Communications, № 18 (2008): 2132. http://dx.doi.org/10.1039/b801524d.
Повний текст джерелаMereshchenko, Andrey S., Alexey V. Ivanov, Viktor I. Baranovskii, Grzegorz Mloston, Ludmila L. Rodina, and 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 (April 20, 2015): 504–13. http://dx.doi.org/10.3762/bjoc.11.57.
Повний текст джерелаColeman, Robert S., and 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, no. 23 (November 1992): 9229–30. http://dx.doi.org/10.1021/ja00049a089.
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