Статті в журналах з теми "Aromatic Carbamates"
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Tietze, Lutz F., Heiko J. Schuster, J. Marian von Hof, Sonja M. Hampel, Juan F. Colunga, and Michael John. "Atropisomerism of Aromatic Carbamates." Chemistry – A European Journal 16, no. 42 (September 30, 2010): 12678–82. http://dx.doi.org/10.1002/chem.201001047.
Повний текст джерелаVincendon, Marc. "Scleroglucan derivatives: Aromatic carbamates." Journal of Polymer Science Part A: Polymer Chemistry 37, no. 16 (August 15, 1999): 3187–92. http://dx.doi.org/10.1002/(sici)1099-0518(19990815)37:16<3187::aid-pola16>3.0.co;2-j.
Повний текст джерелаWilshire, JFK. "The Phthalimidomethyl Rearrangement." Australian Journal of Chemistry 43, no. 11 (1990): 1817. http://dx.doi.org/10.1071/ch9901817.
Повний текст джерелаRojas-Buzo, Sergio, Pilar García-García, and Avelino Corma. "Zr-MOF-808@MCM-41 catalyzed phosgene-free synthesis of polyurethane precursors." Catalysis Science & Technology 9, no. 1 (2019): 146–56. http://dx.doi.org/10.1039/c8cy02235f.
Повний текст джерелаYamagami, C., T. Sai, and N. Takao. "13C N.M.R. Spectra of ortho-Substituted Phenyl N,N-Dimethyl-Carbamates and N-Methyl Carbamates." Australian Journal of Chemistry 40, no. 12 (1987): 2005. http://dx.doi.org/10.1071/ch9872005.
Повний текст джерелаMayer, Szabolcs, Dominika Mária Herr, Nóra Nagy, Viktória Donkó-Tóth, Péter Keglevich, Márton Weber, Miklós Dékány, and László Hazai. "Synthesis and In Vitro Anticancer Evaluation of Chrysin Containing Hybrids and Other Chrysin Derivatives." Periodica Polytechnica Chemical Engineering 67, no. 2 (May 23, 2023): 316–36. http://dx.doi.org/10.3311/ppch.21919.
Повний текст джерелаVELIKORODOV, A. V., T. N. MAKSIMOVA, and V. B. MOCHALIN. "ChemInform Abstract: Reaction of Dichlorocarbene with Aromatic Carbamates." ChemInform 25, no. 38 (August 19, 2010): no. http://dx.doi.org/10.1002/chin.199438131.
Повний текст джерелаKim, Hee-Kwon, and 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, no. 10 (March 6, 2020): 997–1002. http://dx.doi.org/10.1055/s-0040-1707991.
Повний текст джерелаDu, Xiu-Jiang, Qiang Bian, Hong-Xue Wang, Shu-Jing Yu, Jun-Jie Kou, Zhi-Peng Wang, Zheng-Ming Li, and Wei-Guang Zhao. "Design, synthesis, and fungicidal activity of novel carboxylic acid amides represented by N-benzhydryl valinamode carbamates." Org. Biomol. Chem. 12, no. 29 (2014): 5427–34. http://dx.doi.org/10.1039/c4ob00744a.
Повний текст джерелаLi, Qinghe, Peixue Wang, Shimin Liu, Yuqing Fei, and Youquan Deng. "Catalytic degradation of polyurea: synthesis of N-substituted carbamates with CuO–ZnO as the catalyst." Green Chemistry 18, no. 22 (2016): 6091–98. http://dx.doi.org/10.1039/c6gc01884j.
Повний текст джерелаVenkatachalam, TK, P. Samuel, IV Kourinov, and FM Uckun. "Synthesis and Anti-HIV Activity of Carbamates of Antiviral Agent Stavudine." Antiviral Chemistry and Chemotherapy 13, no. 5 (October 2002): 289–97. http://dx.doi.org/10.1177/095632020201300504.
Повний текст джерелаBartolucci, Cecilia, Jure Stojan, Qian-sheng Yu, Nigel H. Greig, and Doriano Lamba. "Kinetics of Torpedo californica acetylcholinesterase inhibition by bisnorcymserine and crystal structure of the complex with its leaving group." Biochemical Journal 444, no. 2 (May 11, 2012): 269–77. http://dx.doi.org/10.1042/bj20111675.
Повний текст джерелаVelikorodov, A. V., E. N. Kutlalieva, N. N. Stepkina, E. A. Shustova, and O. Yu Poddubny. "Amination, Acetamidation, and Amidation of Substituted Aromatic Carbamates in Polyphosphoric Acid." Russian Journal of Organic Chemistry 56, no. 9 (September 2020): 1570–75. http://dx.doi.org/10.1134/s1070428020090110.
Повний текст джерелаVelikorodov, A. V., V. A. Ionova, E. A. Melent’eva, N. N. Stepkina, and A. A. Starikova. "Synthesis of aromatic carbamates derivatives with a chromen-2-one fragment." Russian Journal of Organic Chemistry 50, no. 8 (August 2014): 1112–16. http://dx.doi.org/10.1134/s1070428014080077.
Повний текст джерелаZahedifar, Pegah, Lukasz Pazdur, Christophe M. L. Vande Velde, and Pieter Billen. "Multistage Chemical Recycling of Polyurethanes and Dicarbamates: A Glycolysis–Hydrolysis Demonstration." Sustainability 13, no. 6 (March 23, 2021): 3583. http://dx.doi.org/10.3390/su13063583.
Повний текст джерелаNishizawa, Akihiro, Tsuyoshi Takahira, Kosuke Yasui, Hayato Fujimoto, Tomohiro Iwai, Masaya Sawamura, Naoto Chatani, and Mamoru Tobisu. "Nickel-Catalyzed Decarboxylation of Aryl Carbamates for Converting Phenols into Aromatic Amines." Journal of the American Chemical Society 141, no. 18 (April 21, 2019): 7261–65. http://dx.doi.org/10.1021/jacs.9b02751.
Повний текст джерелаSancha, Shirley A. R., Nikoletta Szemerédi, Gabriella Spengler, and 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, no. 3 (January 20, 2023): 2061. http://dx.doi.org/10.3390/ijms24032061.
Повний текст джерелаTAFESH, A. M., and J. WEIGUNY. "ChemInform Abstract: Selective Catalytic Reduction of Aromatic Nitro Compounds into Aromatic Amines, Isocyanates, Carbamates, and Ureas Using CO." ChemInform 28, no. 3 (August 25, 2010): no. http://dx.doi.org/10.1002/chin.199703321.
Повний текст джерелаZaki, Remon Melad, Adel M. Kamal El-Dean, and Shaban M. Radwan. "SYNTHESIS AND REACTIONS OF SOME NEW MORPHOLINYLPYRROLYL TETRAHYDROTHIENO[2,3-c] ISOQUINOLINE." JOURNAL OF ADVANCES IN CHEMISTRY 10, no. 3 (July 31, 2014): 2512–23. http://dx.doi.org/10.24297/jac.v10i3.6659.
Повний текст джерелаSumita, Akinari, and Tomohiko Ohwada. "Friedel-Crafts-Type Acylation and Amidation Reactions in Strong Brønsted Acid: Taming Superelectrophiles." Molecules 27, no. 18 (September 14, 2022): 5984. http://dx.doi.org/10.3390/molecules27185984.
Повний текст джерелаKrátký, Martin, Šárka Štěpánková, Katarína Vorčáková, Markéta Švarcová, and Jarmila Vinšová. "Novel Cholinesterase Inhibitors Based on O-Aromatic N,N-Disubstituted Carbamates and Thiocarbamates." Molecules 21, no. 2 (February 11, 2016): 191. http://dx.doi.org/10.3390/molecules21020191.
Повний текст джерелаFurer, V. L. "The IR spectra, hydrogen bonding and conformations of aliphatic and aromatic epoxy carbamates." Journal of Molecular Structure 513, no. 1-3 (December 1999): 1–8. http://dx.doi.org/10.1016/s0022-2860(99)00106-4.
Повний текст джерелаGonda, Jozef, and Mariana Barnikol. "Simple and efficient synthesis of 4H-3,1-benzoxazines from 2-bromomethylphenyl isocyanate and amines." Collection of Czechoslovak Chemical Communications 55, no. 3 (1990): 752–60. http://dx.doi.org/10.1135/cccc19900752.
Повний текст джерелаTafesh, Ahmed M., and 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, no. 6 (January 1996): 2035–52. http://dx.doi.org/10.1021/cr950083f.
Повний текст джерелаCenini, Sergio, Corrado Crotti, Maddalena Pizzotti, and Francesca Porta. "Ruthenium carbonyl catalyzed reductive carbonylation of aromatic nitro compounds. A selective route to carbamates." Journal of Organic Chemistry 53, no. 6 (March 1988): 1243–50. http://dx.doi.org/10.1021/jo00241a023.
Повний текст джерелаLapidus, A. L., S. D. Pirozhkov, A. R. Tumanova, A. V. Dolldze, and 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, no. 8 (August 1991): 1672–74. http://dx.doi.org/10.1007/bf01172272.
Повний текст джерелаVigne, B., A. Archelas, and R. Furstoss. "“Microbial transformations 18. Regiospecific para-hydroxylation of aromatic carbamates mediated by the fungus Beauveria sulfurescens”." Tetrahedron 47, no. 8 (January 1991): 1447–58. http://dx.doi.org/10.1016/s0040-4020(01)86421-8.
Повний текст джерелаLAPIDUS, A. L., S. D. PIROZHKOV, A. R. TUMANOVA, A. V. DOLIDZE, and A. M. YUKHIMENKO. "ChemInform Abstract: Synthesis of Carbamates by Carbonylation of Aromatic Nitro Compounds Under Pressure in Cyclohexanol." ChemInform 23, no. 25 (August 21, 2010): no. http://dx.doi.org/10.1002/chin.199225127.
Повний текст джерелаKim, Yoon-Jung, Dong Hoon Lee, Yong-Sung Choi, Jin-Hyun Jeong, and So Hee Kwon. "Benzo[b]tellurophenes as a Potential Histone H3 Lysine 9 Demethylase (KDM4) Inhibitor." International Journal of Molecular Sciences 20, no. 23 (November 25, 2019): 5908. http://dx.doi.org/10.3390/ijms20235908.
Повний текст джерелаSmith, Keith, Gamal El-Hiti, and Mohammed Alshammari. "Unravelling Factors Affecting Directed Lithiation of Acylaminoaromatics." Synthesis 50, no. 18 (March 27, 2018): 3634–52. http://dx.doi.org/10.1055/s-0036-1591954.
Повний текст джерелаARIEL, Naomi, Arie ORDENTLICH, Dov BARAK, Tamar BINO, Baruch VELAN, and 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, no. 1 (October 1, 1998): 95–102. http://dx.doi.org/10.1042/bj3350095.
Повний текст джерелаLi, Fang, Xi Wang, Hongqin Li, Shufang Wang, Wei Xue, and Yanji Wang. "The Induction Period and Novel Active Species in Zn(OAc)2 Catalyzed Synthesis of Aromatic Carbamates." Catalysis Letters 147, no. 6 (April 27, 2017): 1478–84. http://dx.doi.org/10.1007/s10562-017-2055-z.
Повний текст джерелаKurouchi, Hiroaki, Kyoko Kawamoto, Hiromichi Sugimoto, Satoshi Nakamura, Yuko Otani, and 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, no. 20 (October 10, 2012): 9313–28. http://dx.doi.org/10.1021/jo3020566.
Повний текст джерелаTobisu, Mamoru, Keisuke Nakamura, and 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, no. 15 (April 4, 2014): 5587–90. http://dx.doi.org/10.1021/ja501649a.
Повний текст джерелаVIGNE, B., A. ARCHELAS, and R. FURSTOSS. "ChemInform Abstract: Microbial Transformations. Part 18. Regiospecific para-Hydroxylation of Aromatic Carbamates Mediated by the Fungus Beauveria sulfurescens." ChemInform 22, no. 21 (August 23, 2010): no. http://dx.doi.org/10.1002/chin.199121112.
Повний текст джерелаWang, Binshen, Sijuan Yang, Lijun Min, Yanlong Gu, Yongya Zhang, Xiaopei Wu, Lifeng Zhang, Elnazeer H. M. Elageed, Shi Wu, and 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, no. 14-15 (August 19, 2014): 3125–34. http://dx.doi.org/10.1002/adsc.201400026.
Повний текст джерелаTobisu, Mamoru, Keisuke Nakamura, and Naoto Chatani. "ChemInform Abstract: Nickel-Catalyzed Reductive and Borylative Cleavage of Aromatic Carbon-Nitrogen Bonds in N-Aryl Amides and Carbamates." ChemInform 45, no. 42 (October 2, 2014): no. http://dx.doi.org/10.1002/chin.201442203.
Повний текст джерелаSchnell, Sabine, Doris Schiedek, Rolf Schneider, Lennart Balk, Pekka J. Vuorinen, Heta Karvinen, and Thomas Lang. "Biological indications of contaminant exposure in Atlantic cod (Gadus morhua) in the Baltic Sea." Canadian Journal of Fisheries and Aquatic Sciences 65, no. 6 (June 2008): 1122–34. http://dx.doi.org/10.1139/f08-042.
Повний текст джерелаYoshimura, Akira, Matthew W. Luedtke та 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, № 4 (9 лютого 2012): 2087–91. http://dx.doi.org/10.1021/jo300007c.
Повний текст джерелаWang, Binshen, Sijuan Yang, Lijun Min, Yanlong Gu, Yongya Zhang, Xiaopei Wu, Lifeng Zhang, Elnazeer H. M. Elageed, Shi Wu, and 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, no. 12 (March 2015): no. http://dx.doi.org/10.1002/chin.201512254.
Повний текст джерелаMishra, Vivek, Jin Ku Cho, Seung-Han Shin, Young-Woong Suh, Hoon Sik Kim, and 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 (October 2014): 82–90. http://dx.doi.org/10.1016/j.apcata.2014.09.013.
Повний текст джерелаAresta, Michele, Angela Dibenedetto, and 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, no. 20 (1995): 3359. http://dx.doi.org/10.1039/dt9950003359.
Повний текст джерелаKinarivala, Nihar, Ronak Patel, Rose-Mary Boustany, Abraham Al-Ahmad, and 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, no. 23 (November 22, 2017): 9739–56. http://dx.doi.org/10.1021/acs.jmedchem.7b01199.
Повний текст джерелаYoshimura, Akira, Matthew W. Luedtke та 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, № 23 (10 травня 2012): no. http://dx.doi.org/10.1002/chin.201223090.
Повний текст джерелаSingh, 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, no. 1 (August 1, 2018): 37–51. http://dx.doi.org/10.1007/s11224-018-1171-8.
Повний текст джерелаARESTA, M., A. DIBENEDETTO, and 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, no. 7 (August 12, 2010): no. http://dx.doi.org/10.1002/chin.199607210.
Повний текст джерелаMochizuki, Amane, Masahiro Yoshioka, Michie Sakamoto, Takahiro Fukuoka, and Mitsuru Ueda. "One-Pot Synthesis of Aromatic Polycarbodiimide by in Situ Activation of Diamine." High Performance Polymers 10, no. 1 (March 1998): 51–59. http://dx.doi.org/10.1088/0954-0083/10/1/007.
Повний текст джерелаBlencowe, Christopher A., David W. Thornthwaite, Wayne Hayes, and Andrew T. Russell. "Self-immolative base-mediated conjugate release from triazolylmethylcarbamates." Organic & Biomolecular Chemistry 13, no. 32 (2015): 8703–7. http://dx.doi.org/10.1039/c5ob00984g.
Повний текст джерелаLee, Kyu Hyung, Sun Joo Kim, Hee Sun Park, Byung Wook Lim, Byeongno Lee, Young Jun Park, Wonwoo Nam, and Nam Hwi Hur. "Stable carbamate pathway towards organic–inorganic hybrid perovskites and aromatic imines." RSC Advances 10, no. 62 (2020): 38055–62. http://dx.doi.org/10.1039/d0ra07814j.
Повний текст джерелаManikandan, Rajendran, and Masilamani Jeganmohan. "Recent advances in the ruthenium-catalyzed hydroarylation of alkynes with aromatics: synthesis of trisubstituted alkenes." Organic & Biomolecular Chemistry 13, no. 42 (2015): 10420–36. http://dx.doi.org/10.1039/c5ob01472g.
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