Статті в журналах з теми "Catalyzed Transamidation"
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Laclef, Sylvain, Maria Kolympadi Marković, and Dean Marković. "Amide Synthesis by Transamidation of Primary Carboxamides." Synthesis 52, no. 21 (June 4, 2020): 3231–42. http://dx.doi.org/10.1055/s-0040-1707133.
Повний текст джерелаChandrasekaran, Srinivasan, and Rajagopal Ramkumar. "Catalyst-Free, Metal-Free, and Chemoselective Transamidation of Activated Secondary Amides." Synthesis 51, no. 04 (October 18, 2018): 921–32. http://dx.doi.org/10.1055/s-0037-1610664.
Повний текст джерелаSzostak, Michal, and Guangchen Li. "Non-Classical Amide Bond Formation: Transamidation and Amidation of Activated Amides and Esters by Selective N–C/O–C Cleavage." Synthesis 52, no. 18 (May 15, 2020): 2579–99. http://dx.doi.org/10.1055/s-0040-1707101.
Повний текст джерелаRachel, N. M., and J. N. Pelletier. "One-pot peptide and protein conjugation: a combination of enzymatic transamidation and click chemistry." Chemical Communications 52, no. 12 (2016): 2541–44. http://dx.doi.org/10.1039/c5cc09163b.
Повний текст джерелаSharma, Manu, Harikrishnan K, Umesh Kumar Gaur, and Ashok K. Ganguli. "Synthesis of mesoporous SiO2–CeO2 hybrid nanostructures with high catalytic activity for transamidation reaction." RSC Advances 13, no. 19 (2023): 13134–41. http://dx.doi.org/10.1039/d3ra01552a.
Повний текст джерелаDander, Jacob E., Emma L. Baker, and Neil K. Garg. "Nickel-catalyzed transamidation of aliphatic amide derivatives." Chemical Science 8, no. 9 (2017): 6433–38. http://dx.doi.org/10.1039/c7sc01980g.
Повний текст джерелаYang, Dahyeon, Taeil Shin, Hyunwoo Kim, and Sunwoo Lee. "Nickel/briphos-catalyzed transamidation of unactivated tertiary amides." Organic & Biomolecular Chemistry 18, no. 31 (2020): 6053–57. http://dx.doi.org/10.1039/d0ob01271h.
Повний текст джерелаOjeda-Porras, Andrea, and Diego Gamba-Sánchez. "Transamidation of thioacetamide catalyzed by SbCl3." Tetrahedron Letters 56, no. 29 (July 2015): 4308–11. http://dx.doi.org/10.1016/j.tetlet.2015.05.067.
Повний текст джерелаYedage, Subhash L., Denvert S. D'silva, and Bhalchandra M. Bhanage. "MnO2 catalyzed formylation of amines and transamidation of amides under solvent-free conditions." RSC Advances 5, no. 98 (2015): 80441–49. http://dx.doi.org/10.1039/c5ra13094h.
Повний текст джерелаArefi, Marzban, and Akbar Heydari. "Transamidation of primary carboxamides, phthalimide, urea and thiourea with amines using Fe(OH)3@Fe3O4 magnetic nanoparticles as an efficient recyclable catalyst." RSC Advances 6, no. 29 (2016): 24684–89. http://dx.doi.org/10.1039/c5ra27680b.
Повний текст джерелаYang, Xin, Linlin Fan, and Ying Xue. "Mechanistic insights into l-proline-catalyzed transamidation of carboxamide with benzylamine from density functional theory calculations." RSC Adv. 4, no. 57 (2014): 30108–17. http://dx.doi.org/10.1039/c4ra04105d.
Повний текст джерелаGuo, Weijie, Jingjun Huang, Hongxiang Wu, Tingting Liu, Zhongfeng Luo, Junsheng Jian, and Zhuo Zeng. "One-pot transition-metal free transamidation to sterically hindered amides." Organic Chemistry Frontiers 5, no. 20 (2018): 2950–54. http://dx.doi.org/10.1039/c8qo00591e.
Повний текст джерелаFeng, Fang-Fang, Xuan-Yu Liu, Chi Wai Cheung, and Jun-An Ma. "Tungsten-Catalyzed Transamidation of Tertiary Alkyl Amides." ACS Catalysis 11, no. 12 (June 2, 2021): 7070–79. http://dx.doi.org/10.1021/acscatal.1c01840.
Повний текст джерелаYang, Yang, Jian Liu, Fadhil S. Kamounah, Gianluca Ciancaleoni, and Ji-Woong Lee. "A CO2-Catalyzed Transamidation Reaction." Journal of Organic Chemistry 86, no. 23 (November 1, 2021): 16867–81. http://dx.doi.org/10.1021/acs.joc.1c02077.
Повний текст джерелаVanjari, Rajeshwer, Bharat Kumar Allam, and Krishna Nand Singh. "Hypervalent iodine catalyzed transamidation of carboxamides with amines." RSC Adv. 3, no. 6 (2013): 1691–94. http://dx.doi.org/10.1039/c2ra22459c.
Повний текст джерелаSkoczinski, Pia, Mónica K. Espinoza Cangahuala, Dina Maniar, and Katja Loos. "Lipase-Catalyzed Transamidation of Urethane-Bond-Containing Ester." ACS Omega 5, no. 3 (December 23, 2019): 1488–95. http://dx.doi.org/10.1021/acsomega.9b03203.
Повний текст джерелаOjeda-Porras, Andrea, and Diego Gamba-Sanchez. "ChemInform Abstract: Transamidation of Thioacetamide Catalyzed by SbCl3." ChemInform 46, no. 43 (October 2015): no. http://dx.doi.org/10.1002/chin.201543076.
Повний текст джерелаRao, Sadu Nageswara, Darapaneni Chandra Mohan та Subbarayappa Adimurthy. "H-β-zeolite catalyzed transamidation of carboxamides, phthalimide, formamides and thioamides with amines under neat conditions". RSC Advances 5, № 115 (2015): 95313–17. http://dx.doi.org/10.1039/c5ra16933j.
Повний текст джерелаLiu, Juyan, and Congying Zhao. "Lactic Acid-Catalyzed Transamidation Reactions of Carboxamides with Amines." Chinese Journal of Organic Chemistry 41, no. 6 (2021): 2310. http://dx.doi.org/10.6023/cjoc202010010.
Повний текст джерелаBecerra-Figueroa, Liliana, Andrea Ojeda-Porras, and Diego Gamba-Sánchez. "Transamidation of Carboxamides Catalyzed by Fe(III) and Water." Journal of Organic Chemistry 79, no. 10 (May 5, 2014): 4544–52. http://dx.doi.org/10.1021/jo500562w.
Повний текст джерелаCheung, Chi Wai, Marten Leendert Ploeger, and Xile Hu. "Nickel-Catalyzed Reductive Transamidation of Secondary Amides with Nitroarenes." ACS Catalysis 7, no. 10 (September 22, 2017): 7092–96. http://dx.doi.org/10.1021/acscatal.7b02859.
Повний текст джерелаHoerter, Justin M., Karin M. Otte, Samuel H. Gellman, and Shannon S. Stahl. "Mechanism of AlIII-Catalyzed Transamidation of Unactivated Secondary Carboxamides." Journal of the American Chemical Society 128, no. 15 (April 2006): 5177–83. http://dx.doi.org/10.1021/ja060331x.
Повний текст джерелаTian, Qingqiang, Zongjie Gan, Xuetong Wang, Dan Li, Wen Luo, Huajun Wang, Zeshu Dai, and Jianyong Yuan. "Imidazolium Chloride: An Efficient Catalyst for Transamidation of Primary Amines." Molecules 23, no. 9 (September 2, 2018): 2234. http://dx.doi.org/10.3390/molecules23092234.
Повний текст джерелаDing, Wen, Shaoyu Mai, and Qiuling Song. "Molecular-oxygen-promoted Cu-catalyzed oxidative direct amidation of nonactivated carboxylic acids with azoles." Beilstein Journal of Organic Chemistry 11 (November 11, 2015): 2158–65. http://dx.doi.org/10.3762/bjoc.11.233.
Повний текст джерелаAtkinson, Benjamin N., A. Rosie Chhatwal, Helen V. Lomax, James W. Walton, and Jonathan M. J. Williams. "Transamidation of primary amides with amines catalyzed by zirconocene dichloride." Chemical Communications 48, no. 95 (2012): 11626. http://dx.doi.org/10.1039/c2cc37427g.
Повний текст джерелаIordanidou, Domna, Michael G. Kallitsakis, Marina A. Tzani, Dimitris I. Ioannou, Tryfon Zarganes-Tzitzikas, Constantinos G. Neochoritis, Alexander Dömling, Michael A. Terzidis, and Ioannis N. Lykakis. "Supported Gold Nanoparticle-Catalyzed Selective Reduction of Multifunctional, Aromatic Nitro Precursors into Amines and Synthesis of 3,4-Dihydroquinoxalin-2-Ones." Molecules 27, no. 14 (July 8, 2022): 4395. http://dx.doi.org/10.3390/molecules27144395.
Повний текст джерелаBuchspies, Jonathan, Md Mahbubur Rahman, and Michal Szostak. "Transamidation of Amides and Amidation of Esters by Selective N–C(O)/O–C(O) Cleavage Mediated by Air- and Moisture-Stable Half-Sandwich Nickel(II)–NHC Complexes." Molecules 26, no. 1 (January 2, 2021): 188. http://dx.doi.org/10.3390/molecules26010188.
Повний текст джерелаHoerter, Justin M., Karin M. Otte, Samuel H. Gellman, Qiang Cui, and Shannon S. Stahl. "Discovery and Mechanistic Study of AlIII-Catalyzed Transamidation of Tertiary Amides." Journal of the American Chemical Society 130, no. 2 (January 2008): 647–54. http://dx.doi.org/10.1021/ja0762994.
Повний текст джерелаGrover, Rajesh K., Amit P. Kesarwani, Gaurav K. Srivastava, Bijoy Kundu, and Raja Roy. "Base catalyzed intramolecular transamidation of 2-aminoquinazoline derivatives on solid phase." Tetrahedron 61, no. 21 (May 2005): 5011–18. http://dx.doi.org/10.1016/j.tet.2005.03.047.
Повний текст джерелаMa, Juan, Feng Zhang, Jingyu Zhang, and Hang Gong. "Cobalt(II)-Catalyzed N -Acylation of Amines through a Transamidation Reaction." European Journal of Organic Chemistry 2018, no. 35 (June 12, 2018): 4940–48. http://dx.doi.org/10.1002/ejoc.201800253.
Повний текст джерелаBecerra-Figueroa, Liliana, Andrea Ojeda-Porras, and Diego Gamba-Sanchez. "ChemInform Abstract: Transamidation of Carboxamides Catalyzed by Fe(III) and Water." ChemInform 45, no. 45 (October 23, 2014): no. http://dx.doi.org/10.1002/chin.201445062.
Повний текст джерелаYu, Subeen, Taeil Shin, Maosheng Zhang, Yuanzhi Xia, Hyunwoo Kim, and Sunwoo Lee. "Nickel/Briphos-Catalyzed Direct Transamidation of Unactivated Secondary Amides Using Trimethylsilyl Chloride." Organic Letters 20, no. 23 (November 16, 2018): 7563–66. http://dx.doi.org/10.1021/acs.orglett.8b03304.
Повний текст джерелаAtkinson, Benjamin N., A. Rosie Chhatwal, Helen V. Lomax, James W. Walton, and Jonathan M. J. Williams. "ChemInform Abstract: Transamidation of Primary Amides with Amines Catalyzed by Zirconocene Dichloride." ChemInform 44, no. 14 (March 20, 2013): no. http://dx.doi.org/10.1002/chin.201314083.
Повний текст джерелаAyub Ali, Md, S. M. A. Hakim Siddiki, Kenichi Kon, and Ken-ichi Shimizu. "Fe3+-exchanged clay catalyzed transamidation of amides with amines under solvent-free condition." Tetrahedron Letters 55, no. 7 (February 2014): 1316–19. http://dx.doi.org/10.1016/j.tetlet.2013.12.111.
Повний текст джерелаBhattacharya, Suchandra, Pranab Ghosh, and Basudeb Basu. "Graphene oxide (GO) catalyzed transamidation of aliphatic amides: An efficient metal-free procedure." Tetrahedron Letters 59, no. 10 (March 2018): 899–903. http://dx.doi.org/10.1016/j.tetlet.2018.01.060.
Повний текст джерелаWu, Ji-Wei, Ya-Dong Wu, Jian-Jun Dai, and Hua-Jian Xu. "Benzoic Acid-Catalyzed Transamidation Reactions of Carboxamides, Phthalimide, Ureas and Thioamide with Amines." Advanced Synthesis & Catalysis 356, no. 11-12 (June 20, 2014): 2429–36. http://dx.doi.org/10.1002/adsc.201400068.
Повний текст джерелаWagh, Ganesh D., Sagar P. Pathare, and Krishnacharya G. Akamanchi. "Sulfated-Tungstate-Catalyzed Synthesis of Ureas/Thioureas via Transamidation and Synthesis of Forchlorofenuron." ChemistrySelect 3, no. 25 (July 2, 2018): 7049–53. http://dx.doi.org/10.1002/slct.201800954.
Повний текст джерелаMali, Anil S., Krishna Indalkar, and Ganesh U. Chaturbhuj. "Solvent-free, Efficient Transamidation of Carboxamides with Amines Catalyzed by Recyclable Sulfated Polyborate Catalyst." Organic Preparations and Procedures International 53, no. 4 (July 4, 2021): 369–78. http://dx.doi.org/10.1080/00304948.2021.1908047.
Повний текст джерелаShi, Min, and Shi‐Cong Cui. "Transamidation Catalyzed by a Recoverable and Reusable PolyDMAP‐Based Hafnium Chloride and Montmorillonite KSF." Synthetic Communications 35, no. 22 (November 2005): 2847–58. http://dx.doi.org/10.1080/00397910500297180.
Повний текст джерелаÇalimsiz, Selçuk, and Mark A. Lipton. "Synthesis ofN-Fmoc-(2S,3S,4R)-3,4-dimethylglutamine: An Application of Lanthanide-Catalyzed Transamidation." Journal of Organic Chemistry 70, no. 16 (August 2005): 6218–21. http://dx.doi.org/10.1021/jo050518r.
Повний текст джерелаDai, Y., N. L. Dudek, T. B. Patel, and N. A. Muma. "Transglutaminase-Catalyzed Transamidation: A Novel Mechanism for Rac1 Activation by 5-Hydroxytryptamine2A Receptor Stimulation." Journal of Pharmacology and Experimental Therapeutics 326, no. 1 (April 9, 2008): 153–62. http://dx.doi.org/10.1124/jpet.107.135046.
Повний текст джерелаZhang, Min, Sebastian Imm, Sebastian Bähn, Lorenz Neubert, Helfried Neumann, and Matthias Beller. "Efficient Copper(II)-Catalyzed Transamidation of Non-Activated Primary Carboxamides and Ureas with Amines." Angewandte Chemie International Edition 51, no. 16 (March 7, 2012): 3905–9. http://dx.doi.org/10.1002/anie.201108599.
Повний текст джерелаMishra, Ankush, Sundaram Singh, and Vandana Srivastava. "Cerium Catalyzed Transamidation of Secondary Amides under Ultrasound Irradiation: A Breakthrough in Organic Synthesis." Asian Journal of Organic Chemistry 7, no. 8 (June 25, 2018): 1600–1604. http://dx.doi.org/10.1002/ajoc.201800258.
Повний текст джерелаZhang, Min, Sebastian Imm, Sebastian Bähn, Lorenz Neubert, Helfried Neumann, and Matthias Beller. "Efficient Copper(II)-Catalyzed Transamidation of Non-Activated Primary Carboxamides and Ureas with Amines." Angewandte Chemie 124, no. 16 (March 7, 2012): 3971–75. http://dx.doi.org/10.1002/ange.201108599.
Повний текст джерелаWu, Ji-Wei, Ya-Dong Wu, Jian-Jun Dai, and Hua-Jian Xu. "ChemInform Abstract: Benzoic Acid-Catalyzed Transamidation Reactions of Carboxamides, Phthalimide, Ureas and Thioamide with Amines." ChemInform 46, no. 7 (January 29, 2015): no. http://dx.doi.org/10.1002/chin.201507058.
Повний текст джерелаAyub Ali, Md, S. M. A. Hakim Siddiki, Kenichi Kon, and Ken-ichi Shimizu. "ChemInform Abstract: Fe3+-Exchanged Clay Catalyzed Transamidation of Amides with Amines under Solvent-Free Condition." ChemInform 45, no. 31 (July 17, 2014): no. http://dx.doi.org/10.1002/chin.201431086.
Повний текст джерелаWu, Weirong. "Theoretical Insight into the Mechanism of an Efficient ʟ-Proline-catalyzed Transamidation of Acetamide with Benzylamine". Bulletin of the Korean Chemical Society 35, № 9 (20 вересня 2014): 2673–78. http://dx.doi.org/10.5012/bkcs.2014.35.9.2673.
Повний текст джерелаZhang, Min, Sebastian Imm, Sebastian Baehn, Lorenz Neubert, Helfried Neumann, and Matthias Beller. "ChemInform Abstract: Efficient Copper(II)-Catalyzed Transamidation of Non-Activated Primary Carboxamides and Ureas with Amines." ChemInform 43, no. 36 (August 9, 2012): no. http://dx.doi.org/10.1002/chin.201236064.
Повний текст джерелаFu, Renzhong, Yang Yang, Zhikai Chen, Wenchen Lai, Yongfeng Ma, Quan Wang, and Rongxin Yuan. "Microwave-assisted heteropolyanion-based ionic liquids catalyzed transamidation of non-activated carboxamides with amines under solvent-free conditions." Tetrahedron 70, no. 50 (December 2014): 9492–99. http://dx.doi.org/10.1016/j.tet.2014.10.066.
Повний текст джерелаRao, Sadu Nageswara, Darapaneni Chandra Mohan та Subbarayappa Adimurthy. "ChemInform Abstract: H-β-Zeolite Catalyzed Transamidation of Carboxamides, Phthalimide, Formamides and Thioamides with Amines under Neat Conditions." ChemInform 47, № 12 (березень 2016): no. http://dx.doi.org/10.1002/chin.201612077.
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