Статті в журналах з теми "Synthesis of thioamide"
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Dong, Zhi-Bing, Meng-Tian Zeng, Min Wang, Han-Ying Peng, and Yu Cheng. "Copper-Catalyzed Synthesis of Aryl Thioamides from Aryl Aldehydes and Tetramethylthiuram Disulfide." Synthesis 50, no. 03 (October 12, 2017): 644–50. http://dx.doi.org/10.1055/s-0036-1590936.
Повний текст джерелаSauvé, Gilles, Vanga S. Rao, Gilles Lajoie, and Bernard Belleau. "Backbone-modified oligopeptidic bioregulators. The synthesis and configuration of thioamide, amidoxime, cyanoamidine, and amidrazone analogs of the chemotactic peptide N-formyl-methionyl-leucyl-phenylalanine (f-Met-Leu-Phe-OR)." Canadian Journal of Chemistry 63, no. 11 (November 1, 1985): 3089–101. http://dx.doi.org/10.1139/v85-511.
Повний текст джерелаFong, Mei, Wit K. Janowski, Rolf H. Prager, and Max R. Taylor. "A Convenient Synthesis of 2-Substituted Thiazole-5-carboxylates." Australian Journal of Chemistry 57, no. 6 (2004): 599. http://dx.doi.org/10.1071/ch03252.
Повний текст джерелаSzantai-Kis, D., Christopher Walters, Taylor Barrett, Eileen Hoang, and E. Petersson. "Thieme Chemistry Journals Awardees – Where Are They Now? Improved Fmoc Deprotection Methods for the Synthesis of Thioamide-Containing Peptides and Proteins." Synlett 28, no. 14 (May 19, 2017): 1789–94. http://dx.doi.org/10.1055/s-0036-1589027.
Повний текст джерелаZhang, Qiang, Laurent Soulère, and Yves Queneau. "Towards More Practical Methods for the Chemical Synthesis of Thioamides Using Sulfuration Agents: A Decade Update." Molecules 28, no. 8 (April 17, 2023): 3527. http://dx.doi.org/10.3390/molecules28083527.
Повний текст джерелаPham Xuan Thao. "Study on the synthesis of thioamides from aldehyde N-tert-butylsulfinyl amide and sulfur in aqueous media." Journal of Military Science and Technology, no. 76 (December 12, 2021): 54–60. http://dx.doi.org/10.54939/1859-1043.j.mst.76.2021.54-60.
Повний текст джерелаHammam, A. S., and B. E. Bayoumy. "Reaction of thioamides with 2,3-dichloro-1,4-naphthoquinone. A novel synthesis of naphtho[2,3-d]thiazole-4,9-diones." Collection of Czechoslovak Chemical Communications 50, no. 1 (1985): 71–79. http://dx.doi.org/10.1135/cccc19850071.
Повний текст джерелаSharma, Shubham, Dharmender Singh, Sunit Kumar, Vaishali, Rahul Jamra, Naveen Banyal, Deepika, Chandi C. Malakar, and Virender Singh. "An efficient metal-free and catalyst-free C–S/C–O bond-formation strategy: synthesis of pyrazole-conjugated thioamides and amides." Beilstein Journal of Organic Chemistry 19 (March 2, 2023): 231–44. http://dx.doi.org/10.3762/bjoc.19.22.
Повний текст джерелаYeo, Chien, and Edward Tiekink. "O-Methyl m-Tolylcarbamothioate." Molbank 2018, no. 3 (September 15, 2018): M1020. http://dx.doi.org/10.3390/m1020.
Повний текст джерелаCakmak, M., I. I. Ozturk, C. N. Banti, M. Manoli, E. Moushi, A. J. Tasiopoulos, A. M. Grześkiewicz, M. Kubicki, and S. K. Hadjikakou. "Bismuth(III) bromide-thioamide complexes: synthesis, characterization and cytotoxic properties." Main Group Metal Chemistry 41, no. 5-6 (November 27, 2018): 143–54. http://dx.doi.org/10.1515/mgmc-2018-0035.
Повний текст джерелаKumagai, Naoya, Masakatsu Shibasaki, Yuya Ota, and Zhao Li. "Catalytic Asymmetric Synthesis of syn Aldols with Methyl Ketone Functionality and anti Aldols with a Thioamide Group." Synlett 30, no. 05 (February 13, 2019): 620–24. http://dx.doi.org/10.1055/s-0037-1610690.
Повний текст джерелаValdez-Rojas, José Ernesto, Hulme Ríos-Guerra, Alma Leticia Ramírez-Sánchez, Guadalupe García-González, Cecilio Álvarez-Toledano, José Guadalupe López-Cortés, Rubén A. Toscano та José Guillermo Penieres-Carrillo. "A study of the Willgerodt–Kindler reaction to obtain thioamides and α-ketothioamides under solvent-less conditions". Canadian Journal of Chemistry 90, № 7 (липень 2012): 567–73. http://dx.doi.org/10.1139/v2012-030.
Повний текст джерелаRanskiy, Anatoliy, and Natalia Didenko. "Direct Synthesis of Cuprum(II) Complex Compounds Based on Thioamide Ligands." Chemistry & Chemical Technology 8, no. 4 (December 5, 2014): 371–78. http://dx.doi.org/10.23939/chcht08.04.371.
Повний текст джерелаWang, Yanxin J., D. Miklos Szantai-Kis, and E. James Petersson. "Semi-synthesis of thioamide containing proteins." Organic & Biomolecular Chemistry 13, no. 18 (2015): 5074–81. http://dx.doi.org/10.1039/c5ob00224a.
Повний текст джерелаMirjafary, Zohreh, Leila Ahmadi, Masomeh Moradi, and Hamid Saeidian. "A copper(ii)–thioamide combination as a robust heterogeneous catalytic system for green synthesis of 1,4-disubstituted-1,2,3-triazoles under click conditions." RSC Advances 5, no. 95 (2015): 78038–46. http://dx.doi.org/10.1039/c5ra16581d.
Повний текст джерелаYamazaki, Takao, and Hiroki Takahata. "Synthesis of Heterocycles Using Thioamide Groups." HETEROCYCLES 27, no. 8 (1988): 1953. http://dx.doi.org/10.3987/rev-88-387.
Повний текст джерелаTAKAHATA, Hiroki, and Takao YAMAZAKI. "Synthesis of heterocycles using thioamide groups." Journal of Synthetic Organic Chemistry, Japan 45, no. 7 (1987): 682–90. http://dx.doi.org/10.5059/yukigoseikyokaishi.45.682.
Повний текст джерелаVankar, Jigarkumar K., Ankush Gupta, Jaydeepbhai P. Jadav, Shankara H. Nanjegowda, and Guddeangadi N. Gururaja. "The thioamidation of gem-dibromoalkenes in an aqueous medium." Organic & Biomolecular Chemistry 19, no. 11 (2021): 2473–80. http://dx.doi.org/10.1039/d0ob02319a.
Повний текст джерелаDe Zotti, Marta, Barbara Biondi, Cristina Peggion, Matteo De Poli, Haleh Fathi, Simona Oancea, Claudio Toniolo, and Fernando Formaggio. "Partial thioamide scan on the lipopeptaibiotic trichogin GA IV. Effects on folding and bioactivity." Beilstein Journal of Organic Chemistry 8 (July 24, 2012): 1161–71. http://dx.doi.org/10.3762/bjoc.8.129.
Повний текст джерелаLiu, Yinbo, Xiaofeng Mo, Irfan Majeed, Mei Zhang, Hui Wang, and Zhuo Zeng. "An efficient and straightforward approach for accessing thionoesters via palladium-catalyzed C–N cleavage of thioamides." Organic & Biomolecular Chemistry 20, no. 7 (2022): 1532–37. http://dx.doi.org/10.1039/d1ob02349g.
Повний текст джерелаWang, Xi-Cun, Zheng-Jun Quan, Bin Xu, and Xue Zhong. "An Aluminum(III)-Catalyzed Thioamide–Aldehyde–Styrene Condensation: Direct Synthesis of Allylic Thioamide Derivatives." Synlett 27, no. 15 (June 27, 2016): 2237–40. http://dx.doi.org/10.1055/s-0035-1562507.
Повний текст джерелаSzostak, Michal, and Jeffrey Aubé. "Synthesis and rearrangement of a bridged thioamide." Chemical Communications, no. 46 (2009): 7122. http://dx.doi.org/10.1039/b917508c.
Повний текст джерелаDixon, Sally, and Richard J. Whitby. "Efficient synthesis of thioamide terminated molecular wires." Tetrahedron Letters 47, no. 46 (November 2006): 8147–50. http://dx.doi.org/10.1016/j.tetlet.2006.09.032.
Повний текст джерелаShabani, Sadegh, and Craig A. Hutton. "Depsipeptide synthesis using a late-stage Ag(i)-promoted macrolactonisation of peptide thioamides." Chemical Communications 57, no. 16 (2021): 2081–84. http://dx.doi.org/10.1039/d0cc07747j.
Повний текст джерелаBeyzaei, Hamid, Reza Aryan, and Zahra Keshtegar. "Synthesis of New Imidazolidine and Tetrahydropyrimidine Derivatives." Advances in Chemistry 2014 (July 14, 2014): 1–4. http://dx.doi.org/10.1155/2014/834641.
Повний текст джерелаMaini, Rumit, Hiroyuki Kimura, Ryo Takatsuji, Takayuki Katoh, Yuki Goto, and Hiroaki Suga. "Ribosomal Formation of Thioamide Bonds in Polypeptide Synthesis." Journal of the American Chemical Society 141, no. 51 (December 9, 2019): 20004–8. http://dx.doi.org/10.1021/jacs.9b11097.
Повний текст джерелаPoupaert, Jacques H., Sandro Duarte, Evelina Colacino, Patrick Depreux, Christopher R. McCurdy, and Didier L. Lambert. "WILLGERODT-KINDLER'S MICROWAVE-ENHANCED SYNTHESIS OF THIOAMIDE DERIVATIVES." Phosphorus, Sulfur, and Silicon and the Related Elements 179, no. 10 (October 1, 2004): 1959–73. http://dx.doi.org/10.1080/10426500490466995.
Повний текст джерелаBrain, Christopher T., Allan Hallett, and Soo Y. Ko. "Thioamide Synthesis: Thioacyl-N-phthalimides as Thioacylating Agents." Journal of Organic Chemistry 62, no. 12 (June 1997): 3808–9. http://dx.doi.org/10.1021/jo970528v.
Повний текст джерелаWang, Yanxin J., D. Miklos Szantai-Kis, and E. James Petersson. "ChemInform Abstract: Semi-Synthesis of Thioamide Containing Proteins." ChemInform 46, no. 27 (June 18, 2015): no. http://dx.doi.org/10.1002/chin.201527307.
Повний текст джерелаJang, Youngchan, and Richard A. Bartsch. "Synthesis of dibenzocrown ethers with pendant thioamide groups." Journal of Heterocyclic Chemistry 32, no. 5 (September 1995): 1441–44. http://dx.doi.org/10.1002/jhet.5570320505.
Повний текст джерелаSchwehm, Carolin, William Lewis, Alexander J. Blake, Barrie Kellam, and Michael J. Stocks. "Preparation and structural analysis of (±)-cis-ethyl 2-sulfanylidenedecahydro-1,6-naphthyridine-6-carboxylate and (±)-trans-ethyl 2-oxooctahydro-1H-pyrrolo[3,2-c]pyridine-5-carboxylate." Acta Crystallographica Section C Structural Chemistry 70, no. 12 (November 19, 2014): 1161–68. http://dx.doi.org/10.1107/s205322961402436x.
Повний текст джерелаKumar, Ramasamy Raj, Rengan Ramesh, and Jan Grzegorz Małecki. "Versatile coordination ability of thioamide ligand in Ru(ii) complexes: synthesis, computational studies, in vitro anticancer activity and apoptosis induction." New Journal of Chemistry 41, no. 17 (2017): 9130–41. http://dx.doi.org/10.1039/c7nj01828b.
Повний текст джерелаSzesni, Normen, Matthias Drexler, Bernhard Weibert, and Helmut Fischer. "Ethynylthioamide Complexes: Synthesis, Reactivity and an Unusual Coupling Reaction with Diethylaminopropyne." Zeitschrift für Naturforschung B 62, no. 3 (March 1, 2007): 346–56. http://dx.doi.org/10.1515/znb-2007-0307.
Повний текст джерелаLhoták, Pavel, and Antonín Kurfürst. "Synthesis of Luminophores Based on Thiazole Derivatives of PBD." Collection of Czechoslovak Chemical Communications 58, no. 8 (1993): 1898–904. http://dx.doi.org/10.1135/cccc19931898.
Повний текст джерелаFerla, Salvatore, Carmine Varricchio, William Knight, Pui Kei Ho, Fabiana Saporito, Beatrice Tropea, Giulio Fagan, et al. "Structure–Activity Relationship Studies on Novel Antiviral Agents for Norovirus Infections." Microorganisms 9, no. 9 (August 24, 2021): 1795. http://dx.doi.org/10.3390/microorganisms9091795.
Повний текст джерелаSośnicki, Jacek, Tadeusz Jagodziński, and Miroslawa Królikowska. "Thioamide derivatives of cannabinoids. A study of the influence of the thioamide function on regiochemistry in the synthesis of thioamide cannabinoids from 2,4-dihydroxybenzothioamides." Journal of Heterocyclic Chemistry 36, no. 4 (July 1999): 1033–41. http://dx.doi.org/10.1002/jhet.5570360434.
Повний текст джерелаWang, Lu, and Phanstiel. "Synthesis ofN-(Hydroxy)amide- andN-(Hydroxy)thioamide-Containing Peptides." Journal of Organic Chemistry 65, no. 5 (March 2000): 1442–47. http://dx.doi.org/10.1021/jo991589r.
Повний текст джерелаGao, Xiang, Jiao Liu, Xin Zuo, Xinyue Feng, and Ying Gao. "Recent Advances in Synthesis of Benzothiazole Compounds Related to Green Chemistry." Molecules 25, no. 7 (April 5, 2020): 1675. http://dx.doi.org/10.3390/molecules25071675.
Повний текст джерелаSosnicki, Jacek, Tadeusz Jagodzinski, and Miroslawa Krolikowska. "ChemInform Abstract: Thioamide Derivatives of Cannabinoids. A Study of the Influence of the Thioamide Function on Regiochemistry in the Synthesis of Thioamide Cannabinoids from 2,4-Dihydroxybenzothioamides." ChemInform 31, no. 5 (June 11, 2010): no. http://dx.doi.org/10.1002/chin.200005198.
Повний текст джерелаDoležal, Martin, Jiří Hartl, Antonín Lyčka, Vladimír Buchta, and Želmíra Odlerová. "Synthesis and Antituberculotic Properties of Some Substituted Pyrazinecarbothioamides." Collection of Czechoslovak Chemical Communications 61, no. 7 (1996): 1102–8. http://dx.doi.org/10.1135/cccc19961102.
Повний текст джерелаYeo, Chien, and Edward Tiekink. "N-(4-Bromophenyl)methoxycarbothioamide." Molbank 2018, no. 3 (August 17, 2018): M1012. http://dx.doi.org/10.3390/m1012.
Повний текст джерелаEL-Hashash, M. A., Yaser Abdel-moemen El-badry, and J. M. Morsy. "4-(3,4-Dichlorophenyl)-6-(Furan-2-yl)Pyrimidine-2-Thiol as Building Block in Heterocyclic Synthesis." JOURNAL OF ADVANCES IN CHEMISTRY 5, no. 2 (September 17, 2009): 669–77. http://dx.doi.org/10.24297/jac.v5i2.2656.
Повний текст джерелаYang, Jiyoung, Brandon J. Johnson, Allan A. Letourneau, Christopher M. Vogels, Andreas Decken, Felix J. Baerlocher, and Stephen A. Westcott. "Synthesis, Characterisation, and Antifungal Activities of Novel Benzodiazaborines." Australian Journal of Chemistry 68, no. 3 (2015): 366. http://dx.doi.org/10.1071/ch14534.
Повний текст джерелаWei, Jianpeng, Yiming Li, and Xuefeng Jiang. "Aqueous Compatible Protocol to Both Alkyl and Aryl Thioamide Synthesis." Organic Letters 18, no. 2 (January 6, 2016): 340–43. http://dx.doi.org/10.1021/acs.orglett.5b03541.
Повний текст джерелаJANG, Y., and R. A. BARTSCH. "ChemInform Abstract: Synthesis of Dibenzocrown Ethers with Pendant Thioamide Groups." ChemInform 27, no. 13 (August 12, 2010): no. http://dx.doi.org/10.1002/chin.199613185.
Повний текст джерелаBRAIN, C. T., A. HALLETT, and S. Y. KO. "ChemInform Abstract: Thioamide Synthesis: Thioacyl-N-phthalimides as Thioacylating Agents." ChemInform 28, no. 43 (August 3, 2010): no. http://dx.doi.org/10.1002/chin.199743216.
Повний текст джерелаManzor, Kim, and Fintan Kelleher. "Synthesis of orthogonally protected thioamide dipeptides for use in solid-phase peptide synthesis." Tetrahedron Letters 57, no. 47 (November 2016): 5237–39. http://dx.doi.org/10.1016/j.tetlet.2016.10.036.
Повний текст джерелаBasyouni, Wahid Mohamed, and Khairy Abdel-Hamid Mohsen El-Bayouki. "Synthesis of Novel 1,3-thiazole-, 1,2,4-triazole- thione and Triazepine Derivatives." Journal of Chemical Research 2005, no. 6 (June 2005): 356–60. http://dx.doi.org/10.3184/0308234054506730.
Повний текст джерелаMichel, Andre G., Chakib Ameziane-Hassani, Gaston Boulay, and Gilles Lajoie. "Étude structurale de la liaison thioamide: Synthèse et conformation de dérivés de la thioalanine et de la thioglycine." Canadian Journal of Chemistry 67, no. 8 (August 1, 1989): 1312–18. http://dx.doi.org/10.1139/v89-202.
Повний текст джерелаSlouka, Jan, and Vojtěch Bekárek. "Synthesis and cyclization of some N-oxides of 2-pyridylhydrazones of mesoxalic acid derivatives." Collection of Czechoslovak Chemical Communications 53, no. 3 (1988): 626–32. http://dx.doi.org/10.1135/cccc19880626.
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