Статті в журналах з теми "Amidation reactions"
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Liu, Yunyun, and Baoli Zhao. "Step-Economical C–H Activation Reactions Directed by In Situ Amidation." Synthesis 52, no. 21 (May 18, 2020): 3211–18. http://dx.doi.org/10.1055/s-0040-1707124.
Повний текст джерелаGao, Yunling. "A new specific mechanism for thioacid/azide amidation: electronic and solvent effects." Open Chemistry 8, no. 2 (April 1, 2010): 308–19. http://dx.doi.org/10.2478/s11532-009-0139-3.
Повний текст джерелаZhao, Bei, Yang Xiao, Dan Yuan, Chengrong Lu, and Yingming Yao. "Synthesis and characterization of bridged bis(amidato) rare earth metal amides and their applications in C–N bond formation reactions." Dalton Transactions 45, no. 9 (2016): 3880–87. http://dx.doi.org/10.1039/c5dt04217h.
Повний текст джерелаSantos, A. Sofia, Artur M. S. Silva, and M. Manuel B. Marques. "Sustainable Amidation Reactions - Recent Advances." European Journal of Organic Chemistry 2020, no. 17 (April 28, 2020): 2501–16. http://dx.doi.org/10.1002/ejoc.202000106.
Повний текст джерелаKasprzak, Artur, Agnieszka Zuchowska, and Magdalena Poplawska. "Functionalization of graphene: does the organic chemistry matter?" Beilstein Journal of Organic Chemistry 14 (August 2, 2018): 2018–26. http://dx.doi.org/10.3762/bjoc.14.177.
Повний текст джерелаJi, Chong-Lei, Pei-Pei Xie, and Xin Hong. "Computational Study of Mechanism and Thermodynamics of Ni/IPr-Catalyzed Amidation of Esters." Molecules 23, no. 10 (October 18, 2018): 2681. http://dx.doi.org/10.3390/molecules23102681.
Повний текст джерелаPongracz, Tamas, Aswin Verhoeven, Manfred Wuhrer, and Noortje de Haan. "The structure and role of lactone intermediates in linkage-specific sialic acid derivatization reactions." Glycoconjugate Journal 38, no. 2 (January 18, 2021): 157–66. http://dx.doi.org/10.1007/s10719-020-09971-7.
Повний текст джерелаBuhaienko, Ihor, Maksym Kyrylenko, and Volodymyr Mylenkyi. "Mathematical modeling of the technological process and synthesis of the amidation control system." Proceedings of the NTUU “Igor Sikorsky KPI”. Series: Chemical engineering, ecology and resource saving, no. 1 (March 29, 2022): 55–61. http://dx.doi.org/10.20535/2617-9741.1.2022.254159.
Повний текст джерелаArkhipenko, Sergey, Marco T. Sabatini, Andrei S. Batsanov, Valerija Karaluka, Tom D. Sheppard, Henry S. Rzepa, and Andrew Whiting. "Mechanistic insights into boron-catalysed direct amidation reactions." Chemical Science 9, no. 4 (2018): 1058–72. http://dx.doi.org/10.1039/c7sc03595k.
Повний текст джерелаTortajada, Andreu, Marino Börjesson, and Ruben Martin. "Nickel-Catalyzed Reductive Carboxylation and Amidation Reactions." Accounts of Chemical Research 54, no. 20 (September 29, 2021): 3941–52. http://dx.doi.org/10.1021/acs.accounts.1c00480.
Повний текст джерелаKumar, Dhivya, Richard E. Mains та Betty A. Eipper. "60 YEARS OF POMC: From POMC and α-MSH to PAM, molecular oxygen, copper, and vitamin C". Journal of Molecular Endocrinology 56, № 4 (травень 2016): T63—T76. http://dx.doi.org/10.1530/jme-15-0266.
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 джерелаLiu, Yi, Puying Luo, Yang Fu, Tianxin Hao, Xuan Liu, Qiuping Ding, and Yiyuan Peng. "Recent advances in the tandem annulation of 1,3-enynes to functionalized pyridine and pyrrole derivatives." Beilstein Journal of Organic Chemistry 17 (September 22, 2021): 2462–76. http://dx.doi.org/10.3762/bjoc.17.163.
Повний текст джерелаWan, Jie-Ping, and Yanfeng Jing. "Recent advances in copper-catalyzed C–H bond amidation." Beilstein Journal of Organic Chemistry 11 (November 17, 2015): 2209–22. http://dx.doi.org/10.3762/bjoc.11.240.
Повний текст джерелаVishe, Mahesh, Radim Hrdina, Amalia I. Poblador-Bahamonde, Céline Besnard, Laure Guénée, Thomas Bürgi та Jérôme Lacour. "Remote stereoselective deconjugation of α,β-unsaturated esters by simple amidation reactions". Chemical Science 6, № 8 (2015): 4923–28. http://dx.doi.org/10.1039/c5sc01118c.
Повний текст джерелаWang, Xiao. "Challenges and outlook for catalytic direct amidation reactions." Nature Catalysis 2, no. 2 (February 2019): 98–102. http://dx.doi.org/10.1038/s41929-018-0215-1.
Повний текст джерелаRoscales, Silvia, and Aurelio G. Csáky. "How to make C–N bonds using boronic acids and their derivatives without transition metals." Chemical Society Reviews 49, no. 15 (2020): 5159–77. http://dx.doi.org/10.1039/c9cs00735k.
Повний текст джерелаSteven, Alan. "Micelle-Mediated Chemistry in Water for the Synthesis of Drug Candidates." Synthesis 51, no. 13 (May 21, 2019): 2632–47. http://dx.doi.org/10.1055/s-0037-1610714.
Повний текст джерелаZiyaei Halimehjani, Azim, Petr Beier, Maryam Khalili Foumeshi, Ali Alaei та Blanka Klepetářová. "Tandem Alkylation/Michael Addition Reaction of Dithiocarbamic Acids with Alkyl γ-Bromocrotonates: Access to Functionalized 1,3-Thiazolidine-2-thiones". Synthesis 53, № 13 (25 січня 2021): 2219–28. http://dx.doi.org/10.1055/a-1372-1619.
Повний текст джерелаKadari, Lingaswamy, William Erb, Thierry Roisnel, Palakodety Radha Krishna, and Florence Mongin. "Iodoferrocene as a partner in N-arylation of amides." New Journal of Chemistry 44, no. 37 (2020): 15928–41. http://dx.doi.org/10.1039/d0nj03470c.
Повний текст джерелаMa, Nan, Zheyuan Liu, Jianhui Huang, and Yanfeng Dang. "Mechanistic studies of Cp*Ir(iii)/Cp*Rh(iii)-catalyzed branch-selective allylic C–H amidation: why is Cp*Ir(iii) superior to Cp*Rh(iii)?" Organic & Biomolecular Chemistry 19, no. 17 (2021): 3850–58. http://dx.doi.org/10.1039/d1ob00446h.
Повний текст джерелаLin, Chia-Hsin, Bor-Cherng Hong, and Gene-Hsiang Lee. "Asymmetric synthesis of functionalized pyrrolizidines by an organocatalytic and pot-economy strategy." RSC Advances 6, no. 10 (2016): 8243–47. http://dx.doi.org/10.1039/c5ra25103f.
Повний текст джерелаRocco, Daniele, Isabella Chiarotto, Leonardo Mattiello, Fabiana Pandolfi, Daniela Zane, and Marta Feroci. "Electrochemical synthesis and amidation of benzoin: benzamides from benzaldehydes." Pure and Applied Chemistry 91, no. 10 (October 25, 2019): 1709–15. http://dx.doi.org/10.1515/pac-2018-1118.
Повний текст джерелаXia, Ji-Bao, Yan-Lin Li, and Zheng-Yang Gu. "Transition-Metal-Catalyzed Intermolecular C–H Carbonylation toward Amides." Synlett 32, no. 01 (August 17, 2020): 07–13. http://dx.doi.org/10.1055/s-0040-1706416.
Повний текст джерелаMkhonazi, Blessing D., Malibongwe Shandu, Ronewa Tshinavhe, Sandile B. Simelane, and Paseka T. Moshapo. "Solvent-Free Iron(III) Chloride-Catalyzed Direct Amidation of Esters." Molecules 25, no. 5 (February 26, 2020): 1040. http://dx.doi.org/10.3390/molecules25051040.
Повний текст джерелаPaggiola, Giulia, Nolwenn Derrien, Jonathan D. Moseley, Anthony Green, Sabine L. Flitsch, James H. Clark, Con Robert McElroy, and Andrew J. Hunt. "Application of bio-based solvents for biocatalysed synthesis of amides with Pseudomonas stutzeri lipase (PSL)." Pure and Applied Chemistry 92, no. 4 (April 28, 2020): 579–86. http://dx.doi.org/10.1515/pac-2019-0808.
Повний текст джерелаBelousov, Artem S., Anton L. Esipovich, Evgeny A. Kanakov, and Ksenia V. Otopkova. "Recent advances in sustainable production and catalytic transformations of fatty acid methyl esters." Sustainable Energy & Fuels 5, no. 18 (2021): 4512–45. http://dx.doi.org/10.1039/d1se00830g.
Повний текст джерелаKurouchi, Hiroaki. "Diprotonative stabilization of ring-opened carbocationic intermediates: conversion of tetrahydroisoquinoline to triarylmethanes." Chemical Communications 56, no. 59 (2020): 8313–16. http://dx.doi.org/10.1039/d0cc01969k.
Повний текст джерелаMahato, Sachinta, Sougata Santra, Grigory V. Zyryanov, and Adinath Majee. "Metal-Free Amidation Reactions of Terminal Alkynes with Benzenesulfonamide." Journal of Organic Chemistry 84, no. 6 (February 26, 2019): 3176–83. http://dx.doi.org/10.1021/acs.joc.8b03065.
Повний текст джерелаLiu, Bingxian, Bin Li, and Baiquan Wang. "Ru(ii)-catalyzed amidation reactions of 8-methylquinolines with azides via C(sp3)–H activation." Chemical Communications 51, no. 91 (2015): 16334–37. http://dx.doi.org/10.1039/c5cc06230f.
Повний текст джерелаWang, Chao, Lingling Huang, Min Lu, Bei Zhao, Yaorong Wang, Yong Zhang, Qi Shen, and Yingming Yao. "Anionic phenoxy-amido rare-earth complexes as efficient catalysts for amidation of aldehydes with amines." RSC Adv. 5, no. 115 (2015): 94768–75. http://dx.doi.org/10.1039/c5ra20285j.
Повний текст джерелаLi, C., C. D. Oldham та S. W. May. "NN-dimethyl-1,4-phenylenediamine as an alternative reductant for peptidylglycine α-amidating mono-oxygenase catalysis". Biochemical Journal 300, № 1 (15 травня 1994): 31–36. http://dx.doi.org/10.1042/bj3000031.
Повний текст джерелаKasahara, Takahito, and Marco A. Ciufolini. "Further studies toward himandrine via sequential oxidative amidation – intramolecular Diels–Alder reactions." Canadian Journal of Chemistry 91, no. 1 (January 2013): 82–90. http://dx.doi.org/10.1139/cjc-2012-0340.
Повний текст джерелаBera, Shyamal Kanti, Rosalin Bhanja, and Prasenjit Mal. "DDQ in mechanochemical C–N coupling reactions." Beilstein Journal of Organic Chemistry 18 (June 1, 2022): 639–46. http://dx.doi.org/10.3762/bjoc.18.64.
Повний текст джерелаMOORE, Allison B., and Sheldon W. MAY. "Kinetic and inhibition studies on substrate channelling in the bifunctional enzyme catalysing C-terminal amidation." Biochemical Journal 341, no. 1 (June 24, 1999): 33–40. http://dx.doi.org/10.1042/bj3410033.
Повний текст джерелаChen, Mei-Lan, Jian-Qing Min, Sheng-Dong Pan, and Mi-Cong Jin. "Surface core–shell magnetic polymer modified graphene oxide-based material for 2,4,6-trichlorophenol removal." RSC Advances 4, no. 108 (2014): 63494–501. http://dx.doi.org/10.1039/c4ra14150d.
Повний текст джерелаWang, Danfeng, Hai Huang, and Xiaolin Zhu. "Development of anthrazoline photocatalysts for promoting amination and amidation reactions." Chemical Communications 58, no. 21 (2022): 3529–32. http://dx.doi.org/10.1039/d1cc07315j.
Повний текст джерелаHernández, José G., Karen J. Ardila-Fierro, Dajana Barišić, and Hervé Geneste. "Multi-faceted reactivity of N-fluorobenzenesulfonimide (NFSI) under mechanochemical conditions: fluorination, fluorodemethylation, sulfonylation, and amidation reactions." Beilstein Journal of Organic Chemistry 18 (February 7, 2022): 182–89. http://dx.doi.org/10.3762/bjoc.18.20.
Повний текст джерелаYoshino, Tatsuhiko, and Shigeki Matsunaga. "Cp*CoIII-Catalyzed C–H Functionalization and Asymmetric Reactions Using External Chiral Sources." Synlett 30, no. 12 (May 7, 2019): 1384–400. http://dx.doi.org/10.1055/s-0037-1611814.
Повний текст джерелаMartin, Stephen F., Michael P. Dwyer, and Christopher L. Lynch. "Application of AlMe3-mediated amidation reactions to solution phase peptide synthesis." Tetrahedron Letters 39, no. 12 (March 1998): 1517–20. http://dx.doi.org/10.1016/s0040-4039(98)00071-9.
Повний текст джерелаGaniek, Maximilian A., Matthias R. Becker, Guillaume Berionni, Hendrik Zipse, and Paul Knochel. "Barbier Continuous Flow Preparation and Reactions of Carbamoyllithiums for Nucleophilic Amidation." Chemistry – A European Journal 23, no. 43 (July 17, 2017): 10280–84. http://dx.doi.org/10.1002/chem.201702593.
Повний текст джерелаLamani, Manjunath, and Kandikere Ramaiah Prabhu. "NIS-Catalyzed Reactions: Amidation of Acetophenones and Oxidative Amination of Propiophenones." Chemistry - A European Journal 18, no. 46 (October 5, 2012): 14638–42. http://dx.doi.org/10.1002/chem.201202703.
Повний текст джерелаCho, Inha, Zhi-Jun Jia, and Frances H. Arnold. "Site-selective enzymatic C‒H amidation for synthesis of diverse lactams." Science 364, no. 6440 (May 9, 2019): 575–78. http://dx.doi.org/10.1126/science.aaw9068.
Повний текст джерелаVázquez, Ester, and Maurizio Prato. "Functionalization of carbon nanotubes for applications in materials science and nanomedicine." Pure and Applied Chemistry 82, no. 4 (March 13, 2010): 853–61. http://dx.doi.org/10.1351/pac-con-09-10-40.
Повний текст джерелаGoodreid, Jordan D., Petar A. Duspara, Caroline Bosch, and Robert A. Batey. "Amidation Reactions from the Direct Coupling of Metal Carboxylate Salts with Amines." Journal of Organic Chemistry 79, no. 3 (January 13, 2014): 943–54. http://dx.doi.org/10.1021/jo402374c.
Повний текст джерелаChou, Wen-Chih, Ming-Chen Chou, Yann-Yu Lu, and Shyh-Fong Chen. "HMDS-promotedin situ amidation reactions of car☐ylic acids and amines." Tetrahedron Letters 40, no. 17 (April 1999): 3419–22. http://dx.doi.org/10.1016/s0040-4039(99)00505-5.
Повний текст джерелаBarfoot, Christopher, Gerald Brooks, Pamela Brown, Steven Dabbs, David T. Davies, Ilaria Giordano, Alan Hennessy, et al. "Flexible palladium-catalysed amidation reactions for the synthesis of complex aryl amides." Tetrahedron Letters 51, no. 20 (May 2010): 2685–89. http://dx.doi.org/10.1016/j.tetlet.2010.03.051.
Повний текст джерелаTrumbo, David L. "Polymers based on methyl acrylamidoglycolate methyl ether (MAGME): Michael addition-amidation reactions." Polymer Bulletin 31, no. 5 (November 1993): 523–29. http://dx.doi.org/10.1007/bf00297887.
Повний текст джерелаNguyen, Thanh V., and Demelza J. M. Lyons. "A novel aromatic carbocation-based coupling reagent for esterification and amidation reactions." Chemical Communications 51, no. 15 (2015): 3131–34. http://dx.doi.org/10.1039/c4cc09539a.
Повний текст джерелаRajabi, Fatemeh, Mojdeh Raessi, Rick A. D. Arancon, Mohammad Reza Saidi, and Rafael Luque. "Supported cobalt oxide nanoparticles as efficient catalyst in esterification and amidation reactions." Catalysis Communications 59 (January 2015): 122–26. http://dx.doi.org/10.1016/j.catcom.2014.09.044.
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