Artículos de revistas sobre el tema "Aromatic Carbamates"
Crea una cita precisa en los estilos APA, MLA, Chicago, Harvard y otros
Consulte los 50 mejores artículos de revistas para su investigación sobre el tema "Aromatic Carbamates".
Junto a cada fuente en la lista de referencias hay un botón "Agregar a la bibliografía". Pulsa este botón, y generaremos automáticamente la referencia bibliográfica para la obra elegida en el estilo de cita que necesites: APA, MLA, Harvard, Vancouver, Chicago, etc.
También puede descargar el texto completo de la publicación académica en formato pdf y leer en línea su resumen siempre que esté disponible en los metadatos.
Explore artículos de revistas sobre una amplia variedad de disciplinas y organice su bibliografía correctamente.
Tietze, Lutz F., Heiko J. Schuster, J. Marian von Hof, Sonja M. Hampel, Juan F. Colunga y Michael John. "Atropisomerism of Aromatic Carbamates". Chemistry – A European Journal 16, n.º 42 (30 de septiembre de 2010): 12678–82. http://dx.doi.org/10.1002/chem.201001047.
Texto completoVincendon, Marc. "Scleroglucan derivatives: Aromatic carbamates". Journal of Polymer Science Part A: Polymer Chemistry 37, n.º 16 (15 de agosto de 1999): 3187–92. http://dx.doi.org/10.1002/(sici)1099-0518(19990815)37:16<3187::aid-pola16>3.0.co;2-j.
Texto completoWilshire, JFK. "The Phthalimidomethyl Rearrangement". Australian Journal of Chemistry 43, n.º 11 (1990): 1817. http://dx.doi.org/10.1071/ch9901817.
Texto completoRojas-Buzo, Sergio, Pilar García-García y Avelino Corma. "Zr-MOF-808@MCM-41 catalyzed phosgene-free synthesis of polyurethane precursors". Catalysis Science & Technology 9, n.º 1 (2019): 146–56. http://dx.doi.org/10.1039/c8cy02235f.
Texto completoYamagami, C., T. Sai y N. Takao. "13C N.M.R. Spectra of ortho-Substituted Phenyl N,N-Dimethyl-Carbamates and N-Methyl Carbamates". Australian Journal of Chemistry 40, n.º 12 (1987): 2005. http://dx.doi.org/10.1071/ch9872005.
Texto completoMayer, Szabolcs, Dominika Mária Herr, Nóra Nagy, Viktória Donkó-Tóth, Péter Keglevich, Márton Weber, Miklós Dékány y László Hazai. "Synthesis and In Vitro Anticancer Evaluation of Chrysin Containing Hybrids and Other Chrysin Derivatives". Periodica Polytechnica Chemical Engineering 67, n.º 2 (23 de mayo de 2023): 316–36. http://dx.doi.org/10.3311/ppch.21919.
Texto completoVELIKORODOV, A. V., T. N. MAKSIMOVA y V. B. MOCHALIN. "ChemInform Abstract: Reaction of Dichlorocarbene with Aromatic Carbamates." ChemInform 25, n.º 38 (19 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199438131.
Texto completoKim, Hee-Kwon y Tien Tan Bui. "Lanthanum(III) Trifluoromethanesulfonate Catalyzed Direct Synthesis of Ureas from N-Benzyloxycarbonyl-, N-Allyloxycarbonyl-, and N-2,2,2-Trichloroethoxycarbonyl-Protected Amines". Synlett 31, n.º 10 (6 de marzo de 2020): 997–1002. http://dx.doi.org/10.1055/s-0040-1707991.
Texto completoDu, Xiu-Jiang, Qiang Bian, Hong-Xue Wang, Shu-Jing Yu, Jun-Jie Kou, Zhi-Peng Wang, Zheng-Ming Li y Wei-Guang Zhao. "Design, synthesis, and fungicidal activity of novel carboxylic acid amides represented by N-benzhydryl valinamode carbamates". Org. Biomol. Chem. 12, n.º 29 (2014): 5427–34. http://dx.doi.org/10.1039/c4ob00744a.
Texto completoLi, Qinghe, Peixue Wang, Shimin Liu, Yuqing Fei y Youquan Deng. "Catalytic degradation of polyurea: synthesis of N-substituted carbamates with CuO–ZnO as the catalyst". Green Chemistry 18, n.º 22 (2016): 6091–98. http://dx.doi.org/10.1039/c6gc01884j.
Texto completoVenkatachalam, TK, P. Samuel, IV Kourinov y FM Uckun. "Synthesis and Anti-HIV Activity of Carbamates of Antiviral Agent Stavudine". Antiviral Chemistry and Chemotherapy 13, n.º 5 (octubre de 2002): 289–97. http://dx.doi.org/10.1177/095632020201300504.
Texto completoBartolucci, Cecilia, Jure Stojan, Qian-sheng Yu, Nigel H. Greig y Doriano Lamba. "Kinetics of Torpedo californica acetylcholinesterase inhibition by bisnorcymserine and crystal structure of the complex with its leaving group". Biochemical Journal 444, n.º 2 (11 de mayo de 2012): 269–77. http://dx.doi.org/10.1042/bj20111675.
Texto completoVelikorodov, A. V., E. N. Kutlalieva, N. N. Stepkina, E. A. Shustova y O. Yu Poddubny. "Amination, Acetamidation, and Amidation of Substituted Aromatic Carbamates in Polyphosphoric Acid". Russian Journal of Organic Chemistry 56, n.º 9 (septiembre de 2020): 1570–75. http://dx.doi.org/10.1134/s1070428020090110.
Texto completoVelikorodov, A. V., V. A. Ionova, E. A. Melent’eva, N. N. Stepkina y A. A. Starikova. "Synthesis of aromatic carbamates derivatives with a chromen-2-one fragment". Russian Journal of Organic Chemistry 50, n.º 8 (agosto de 2014): 1112–16. http://dx.doi.org/10.1134/s1070428014080077.
Texto completoZahedifar, Pegah, Lukasz Pazdur, Christophe M. L. Vande Velde y Pieter Billen. "Multistage Chemical Recycling of Polyurethanes and Dicarbamates: A Glycolysis–Hydrolysis Demonstration". Sustainability 13, n.º 6 (23 de marzo de 2021): 3583. http://dx.doi.org/10.3390/su13063583.
Texto completoNishizawa, Akihiro, Tsuyoshi Takahira, Kosuke Yasui, Hayato Fujimoto, Tomohiro Iwai, Masaya Sawamura, Naoto Chatani y Mamoru Tobisu. "Nickel-Catalyzed Decarboxylation of Aryl Carbamates for Converting Phenols into Aromatic Amines". Journal of the American Chemical Society 141, n.º 18 (21 de abril de 2019): 7261–65. http://dx.doi.org/10.1021/jacs.9b02751.
Texto completoSancha, Shirley A. R., Nikoletta Szemerédi, Gabriella Spengler y Maria-José U. Ferreira. "Lycorine Carbamate Derivatives for Reversing P-Glycoprotein-Mediated Multidrug Resistance in Human Colon Adenocarcinoma Cells". International Journal of Molecular Sciences 24, n.º 3 (20 de enero de 2023): 2061. http://dx.doi.org/10.3390/ijms24032061.
Texto completoTAFESH, A. M. y J. WEIGUNY. "ChemInform Abstract: Selective Catalytic Reduction of Aromatic Nitro Compounds into Aromatic Amines, Isocyanates, Carbamates, and Ureas Using CO". ChemInform 28, n.º 3 (25 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199703321.
Texto completoZaki, Remon Melad, Adel M. Kamal El-Dean y Shaban M. Radwan. "SYNTHESIS AND REACTIONS OF SOME NEW MORPHOLINYLPYRROLYL TETRAHYDROTHIENO[2,3-c] ISOQUINOLINE". JOURNAL OF ADVANCES IN CHEMISTRY 10, n.º 3 (31 de julio de 2014): 2512–23. http://dx.doi.org/10.24297/jac.v10i3.6659.
Texto completoSumita, Akinari y Tomohiko Ohwada. "Friedel-Crafts-Type Acylation and Amidation Reactions in Strong Brønsted Acid: Taming Superelectrophiles". Molecules 27, n.º 18 (14 de septiembre de 2022): 5984. http://dx.doi.org/10.3390/molecules27185984.
Texto completoKrátký, Martin, Šárka Štěpánková, Katarína Vorčáková, Markéta Švarcová y Jarmila Vinšová. "Novel Cholinesterase Inhibitors Based on O-Aromatic N,N-Disubstituted Carbamates and Thiocarbamates". Molecules 21, n.º 2 (11 de febrero de 2016): 191. http://dx.doi.org/10.3390/molecules21020191.
Texto completoFurer, V. L. "The IR spectra, hydrogen bonding and conformations of aliphatic and aromatic epoxy carbamates". Journal of Molecular Structure 513, n.º 1-3 (diciembre de 1999): 1–8. http://dx.doi.org/10.1016/s0022-2860(99)00106-4.
Texto completoGonda, Jozef y Mariana Barnikol. "Simple and efficient synthesis of 4H-3,1-benzoxazines from 2-bromomethylphenyl isocyanate and amines". Collection of Czechoslovak Chemical Communications 55, n.º 3 (1990): 752–60. http://dx.doi.org/10.1135/cccc19900752.
Texto completoTafesh, Ahmed M. y Jens Weiguny. "A Review of the Selective Catalytic Reduction of Aromatic Nitro Compounds into Aromatic Amines, Isocyanates, Carbamates, and Ureas Using CO†". Chemical Reviews 96, n.º 6 (enero de 1996): 2035–52. http://dx.doi.org/10.1021/cr950083f.
Texto completoCenini, Sergio, Corrado Crotti, Maddalena Pizzotti y Francesca Porta. "Ruthenium carbonyl catalyzed reductive carbonylation of aromatic nitro compounds. A selective route to carbamates". Journal of Organic Chemistry 53, n.º 6 (marzo de 1988): 1243–50. http://dx.doi.org/10.1021/jo00241a023.
Texto completoLapidus, A. L., S. D. Pirozhkov, A. R. Tumanova, A. V. Dolldze y A. M. Yukhimenko. "High-pressure synthesis of carbamates by the carbonylation of aromatic nitro compounds in cyclohexanol". Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 40, n.º 8 (agosto de 1991): 1672–74. http://dx.doi.org/10.1007/bf01172272.
Texto completoVigne, B., A. Archelas y R. Furstoss. "“Microbial transformations 18. Regiospecific para-hydroxylation of aromatic carbamates mediated by the fungus Beauveria sulfurescens”". Tetrahedron 47, n.º 8 (enero de 1991): 1447–58. http://dx.doi.org/10.1016/s0040-4020(01)86421-8.
Texto completoLAPIDUS, A. L., S. D. PIROZHKOV, A. R. TUMANOVA, A. V. DOLIDZE y A. M. YUKHIMENKO. "ChemInform Abstract: Synthesis of Carbamates by Carbonylation of Aromatic Nitro Compounds Under Pressure in Cyclohexanol." ChemInform 23, n.º 25 (21 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199225127.
Texto completoKim, Yoon-Jung, Dong Hoon Lee, Yong-Sung Choi, Jin-Hyun Jeong y So Hee Kwon. "Benzo[b]tellurophenes as a Potential Histone H3 Lysine 9 Demethylase (KDM4) Inhibitor". International Journal of Molecular Sciences 20, n.º 23 (25 de noviembre de 2019): 5908. http://dx.doi.org/10.3390/ijms20235908.
Texto completoSmith, Keith, Gamal El-Hiti y Mohammed Alshammari. "Unravelling Factors Affecting Directed Lithiation of Acylaminoaromatics". Synthesis 50, n.º 18 (27 de marzo de 2018): 3634–52. http://dx.doi.org/10.1055/s-0036-1591954.
Texto completoARIEL, Naomi, Arie ORDENTLICH, Dov BARAK, Tamar BINO, Baruch VELAN y Avigdor SHAFFERMAN. "The ‘aromatic patch’ of three proximal residues in the human acetylcholinesterase active centre allows for versatile interaction modes with inhibitors". Biochemical Journal 335, n.º 1 (1 de octubre de 1998): 95–102. http://dx.doi.org/10.1042/bj3350095.
Texto completoLi, Fang, Xi Wang, Hongqin Li, Shufang Wang, Wei Xue y Yanji Wang. "The Induction Period and Novel Active Species in Zn(OAc)2 Catalyzed Synthesis of Aromatic Carbamates". Catalysis Letters 147, n.º 6 (27 de abril de 2017): 1478–84. http://dx.doi.org/10.1007/s10562-017-2055-z.
Texto completoKurouchi, Hiroaki, Kyoko Kawamoto, Hiromichi Sugimoto, Satoshi Nakamura, Yuko Otani y Tomohiko Ohwada. "Activation of Electrophilicity of Stable Y-Delocalized Carbamate Cations in Intramolecular Aromatic Substitution Reaction: Evidence for Formation of Diprotonated Carbamates Leading to Generation of Isocyanates". Journal of Organic Chemistry 77, n.º 20 (10 de octubre de 2012): 9313–28. http://dx.doi.org/10.1021/jo3020566.
Texto completoTobisu, Mamoru, Keisuke Nakamura y Naoto Chatani. "Nickel-Catalyzed Reductive and Borylative Cleavage of Aromatic Carbon–Nitrogen Bonds in N-Aryl Amides and Carbamates". Journal of the American Chemical Society 136, n.º 15 (4 de abril de 2014): 5587–90. http://dx.doi.org/10.1021/ja501649a.
Texto completoVIGNE, B., A. ARCHELAS y R. FURSTOSS. "ChemInform Abstract: Microbial Transformations. Part 18. Regiospecific para-Hydroxylation of Aromatic Carbamates Mediated by the Fungus Beauveria sulfurescens." ChemInform 22, n.º 21 (23 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199121112.
Texto completoWang, Binshen, Sijuan Yang, Lijun Min, Yanlong Gu, Yongya Zhang, Xiaopei Wu, Lifeng Zhang, Elnazeer H. M. Elageed, Shi Wu y Guohua Gao. "Eco-Efficient Synthesis of Cyclic Carbamates/Dithiocarbonimidates from Cyclic Carbonates/Trithiocarbonate and Aromatic Amines Catalyzed by Ionic Liquid BmimOAc". Advanced Synthesis & Catalysis 356, n.º 14-15 (19 de agosto de 2014): 3125–34. http://dx.doi.org/10.1002/adsc.201400026.
Texto completoTobisu, Mamoru, Keisuke Nakamura y Naoto Chatani. "ChemInform Abstract: Nickel-Catalyzed Reductive and Borylative Cleavage of Aromatic Carbon-Nitrogen Bonds in N-Aryl Amides and Carbamates." ChemInform 45, n.º 42 (2 de octubre de 2014): no. http://dx.doi.org/10.1002/chin.201442203.
Texto completoSchnell, Sabine, Doris Schiedek, Rolf Schneider, Lennart Balk, Pekka J. Vuorinen, Heta Karvinen y Thomas Lang. "Biological indications of contaminant exposure in Atlantic cod (Gadus morhua) in the Baltic Sea". Canadian Journal of Fisheries and Aquatic Sciences 65, n.º 6 (junio de 2008): 1122–34. http://dx.doi.org/10.1139/f08-042.
Texto completoYoshimura, Akira, Matthew W. Luedtke y Viktor V. Zhdankin. "(Tosylimino)phenyl-λ3-iodane as a Reagent for the Synthesis of Methyl Carbamates via Hofmann Rearrangement of Aromatic and Aliphatic Carboxamides". Journal of Organic Chemistry 77, n.º 4 (9 de febrero de 2012): 2087–91. http://dx.doi.org/10.1021/jo300007c.
Texto completoWang, Binshen, Sijuan Yang, Lijun Min, Yanlong Gu, Yongya Zhang, Xiaopei Wu, Lifeng Zhang, Elnazeer H. M. Elageed, Shi Wu y Guohua Gao. "ChemInform Abstract: Eco-Efficient Synthesis of Cyclic Carbamates/Dithiocarbonimidates from Cyclic Carbonates/Trithiocarbonate and Aromatic Amines Catalyzed by Ionic Liquid BmimOAc." ChemInform 46, n.º 12 (marzo de 2015): no. http://dx.doi.org/10.1002/chin.201512254.
Texto completoMishra, Vivek, Jin Ku Cho, Seung-Han Shin, Young-Woong Suh, Hoon Sik Kim y Yong Jin Kim. "Ruthenium-Na 2 CO 3 -catalyzed one-pot synthesis of ring-hydrogenated carbamates from aromatic amines and organic carbonates under H 2". Applied Catalysis A: General 487 (octubre de 2014): 82–90. http://dx.doi.org/10.1016/j.apcata.2014.09.013.
Texto completoAresta, Michele, Angela Dibenedetto y Eugenio Quaranta. "Reaction of alkali-metal tetraphenylborates with amines in the presence of CO2: a new easy way to aliphatic and aromatic alkali-metal carbamates". Journal of the Chemical Society, Dalton Transactions, n.º 20 (1995): 3359. http://dx.doi.org/10.1039/dt9950003359.
Texto completoKinarivala, Nihar, Ronak Patel, Rose-Mary Boustany, Abraham Al-Ahmad y Paul C. Trippier. "Discovery of Aromatic Carbamates that Confer Neuroprotective Activity by Enhancing Autophagy and Inducing the Anti-Apoptotic Protein B-Cell Lymphoma 2 (Bcl-2)". Journal of Medicinal Chemistry 60, n.º 23 (22 de noviembre de 2017): 9739–56. http://dx.doi.org/10.1021/acs.jmedchem.7b01199.
Texto completoYoshimura, Akira, Matthew W. Luedtke y Viktor V. Zhdankin. "ChemInform Abstract: (Tosylimino)phenyl-λ3-iodane as a Reagent for the Synthesis of Methyl Carbamates via Hofmann Rearrangement of Aromatic and Aliphatic Carboxamides." ChemInform 43, n.º 23 (10 de mayo de 2012): no. http://dx.doi.org/10.1002/chin.201223090.
Texto completoSingh, Harjinder. "The mechanistic study of reaction between N-benzoyl carbamates and aliphatic/aromatic amines for synthesis of substituted N-benzoyl urea derivatives: a DFT approach". Structural Chemistry 30, n.º 1 (1 de agosto de 2018): 37–51. http://dx.doi.org/10.1007/s11224-018-1171-8.
Texto completoARESTA, M., A. DIBENEDETTO y E. QUARANTA. "ChemInform Abstract: Reaction of Alkali-Metal Tetraphenylborates with Amines in the Presence of CO2: A New Easy Way to Aliphatic and Aromatic Alkali-Metal Carbamates." ChemInform 27, n.º 7 (12 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199607210.
Texto completoMochizuki, Amane, Masahiro Yoshioka, Michie Sakamoto, Takahiro Fukuoka y Mitsuru Ueda. "One-Pot Synthesis of Aromatic Polycarbodiimide by in Situ Activation of Diamine". High Performance Polymers 10, n.º 1 (marzo de 1998): 51–59. http://dx.doi.org/10.1088/0954-0083/10/1/007.
Texto completoBlencowe, Christopher A., David W. Thornthwaite, Wayne Hayes y Andrew T. Russell. "Self-immolative base-mediated conjugate release from triazolylmethylcarbamates". Organic & Biomolecular Chemistry 13, n.º 32 (2015): 8703–7. http://dx.doi.org/10.1039/c5ob00984g.
Texto completoLee, Kyu Hyung, Sun Joo Kim, Hee Sun Park, Byung Wook Lim, Byeongno Lee, Young Jun Park, Wonwoo Nam y Nam Hwi Hur. "Stable carbamate pathway towards organic–inorganic hybrid perovskites and aromatic imines". RSC Advances 10, n.º 62 (2020): 38055–62. http://dx.doi.org/10.1039/d0ra07814j.
Texto completoManikandan, Rajendran y Masilamani Jeganmohan. "Recent advances in the ruthenium-catalyzed hydroarylation of alkynes with aromatics: synthesis of trisubstituted alkenes". Organic & Biomolecular Chemistry 13, n.º 42 (2015): 10420–36. http://dx.doi.org/10.1039/c5ob01472g.
Texto completo