Artículos de revistas sobre el tema "Amidation reactions"
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Liu, Yunyun y Baoli Zhao. "Step-Economical C–H Activation Reactions Directed by In Situ Amidation". Synthesis 52, n.º 21 (18 de mayo de 2020): 3211–18. http://dx.doi.org/10.1055/s-0040-1707124.
Texto completoGao, Yunling. "A new specific mechanism for thioacid/azide amidation: electronic and solvent effects". Open Chemistry 8, n.º 2 (1 de abril de 2010): 308–19. http://dx.doi.org/10.2478/s11532-009-0139-3.
Texto completoZhao, Bei, Yang Xiao, Dan Yuan, Chengrong Lu y 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, n.º 9 (2016): 3880–87. http://dx.doi.org/10.1039/c5dt04217h.
Texto completoSantos, A. Sofia, Artur M. S. Silva y M. Manuel B. Marques. "Sustainable Amidation Reactions - Recent Advances". European Journal of Organic Chemistry 2020, n.º 17 (28 de abril de 2020): 2501–16. http://dx.doi.org/10.1002/ejoc.202000106.
Texto completoKasprzak, Artur, Agnieszka Zuchowska y Magdalena Poplawska. "Functionalization of graphene: does the organic chemistry matter?" Beilstein Journal of Organic Chemistry 14 (2 de agosto de 2018): 2018–26. http://dx.doi.org/10.3762/bjoc.14.177.
Texto completoJi, Chong-Lei, Pei-Pei Xie y Xin Hong. "Computational Study of Mechanism and Thermodynamics of Ni/IPr-Catalyzed Amidation of Esters". Molecules 23, n.º 10 (18 de octubre de 2018): 2681. http://dx.doi.org/10.3390/molecules23102681.
Texto completoPongracz, Tamas, Aswin Verhoeven, Manfred Wuhrer y Noortje de Haan. "The structure and role of lactone intermediates in linkage-specific sialic acid derivatization reactions". Glycoconjugate Journal 38, n.º 2 (18 de enero de 2021): 157–66. http://dx.doi.org/10.1007/s10719-020-09971-7.
Texto completoBuhaienko, Ihor, Maksym Kyrylenko y 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, n.º 1 (29 de marzo de 2022): 55–61. http://dx.doi.org/10.20535/2617-9741.1.2022.254159.
Texto completoArkhipenko, Sergey, Marco T. Sabatini, Andrei S. Batsanov, Valerija Karaluka, Tom D. Sheppard, Henry S. Rzepa y Andrew Whiting. "Mechanistic insights into boron-catalysed direct amidation reactions". Chemical Science 9, n.º 4 (2018): 1058–72. http://dx.doi.org/10.1039/c7sc03595k.
Texto completoTortajada, Andreu, Marino Börjesson y Ruben Martin. "Nickel-Catalyzed Reductive Carboxylation and Amidation Reactions". Accounts of Chemical Research 54, n.º 20 (29 de septiembre de 2021): 3941–52. http://dx.doi.org/10.1021/acs.accounts.1c00480.
Texto completoKumar, Dhivya, Richard E. Mains y 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, n.º 4 (mayo de 2016): T63—T76. http://dx.doi.org/10.1530/jme-15-0266.
Texto completoSzostak, Michal y Guangchen Li. "Non-Classical Amide Bond Formation: Transamidation and Amidation of Activated Amides and Esters by Selective N–C/O–C Cleavage". Synthesis 52, n.º 18 (15 de mayo de 2020): 2579–99. http://dx.doi.org/10.1055/s-0040-1707101.
Texto completoLiu, Yi, Puying Luo, Yang Fu, Tianxin Hao, Xuan Liu, Qiuping Ding y Yiyuan Peng. "Recent advances in the tandem annulation of 1,3-enynes to functionalized pyridine and pyrrole derivatives". Beilstein Journal of Organic Chemistry 17 (22 de septiembre de 2021): 2462–76. http://dx.doi.org/10.3762/bjoc.17.163.
Texto completoWan, Jie-Ping y Yanfeng Jing. "Recent advances in copper-catalyzed C–H bond amidation". Beilstein Journal of Organic Chemistry 11 (17 de noviembre de 2015): 2209–22. http://dx.doi.org/10.3762/bjoc.11.240.
Texto completoVishe, Mahesh, Radim Hrdina, Amalia I. Poblador-Bahamonde, Céline Besnard, Laure Guénée, Thomas Bürgi y Jérôme Lacour. "Remote stereoselective deconjugation of α,β-unsaturated esters by simple amidation reactions". Chemical Science 6, n.º 8 (2015): 4923–28. http://dx.doi.org/10.1039/c5sc01118c.
Texto completoWang, Xiao. "Challenges and outlook for catalytic direct amidation reactions". Nature Catalysis 2, n.º 2 (febrero de 2019): 98–102. http://dx.doi.org/10.1038/s41929-018-0215-1.
Texto completoRoscales, Silvia y Aurelio G. Csáky. "How to make C–N bonds using boronic acids and their derivatives without transition metals". Chemical Society Reviews 49, n.º 15 (2020): 5159–77. http://dx.doi.org/10.1039/c9cs00735k.
Texto completoSteven, Alan. "Micelle-Mediated Chemistry in Water for the Synthesis of Drug Candidates". Synthesis 51, n.º 13 (21 de mayo de 2019): 2632–47. http://dx.doi.org/10.1055/s-0037-1610714.
Texto completoZiyaei Halimehjani, Azim, Petr Beier, Maryam Khalili Foumeshi, Ali Alaei y Blanka Klepetářová. "Tandem Alkylation/Michael Addition Reaction of Dithiocarbamic Acids with Alkyl γ-Bromocrotonates: Access to Functionalized 1,3-Thiazolidine-2-thiones". Synthesis 53, n.º 13 (25 de enero de 2021): 2219–28. http://dx.doi.org/10.1055/a-1372-1619.
Texto completoKadari, Lingaswamy, William Erb, Thierry Roisnel, Palakodety Radha Krishna y Florence Mongin. "Iodoferrocene as a partner in N-arylation of amides". New Journal of Chemistry 44, n.º 37 (2020): 15928–41. http://dx.doi.org/10.1039/d0nj03470c.
Texto completoMa, Nan, Zheyuan Liu, Jianhui Huang y 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, n.º 17 (2021): 3850–58. http://dx.doi.org/10.1039/d1ob00446h.
Texto completoLin, Chia-Hsin, Bor-Cherng Hong y Gene-Hsiang Lee. "Asymmetric synthesis of functionalized pyrrolizidines by an organocatalytic and pot-economy strategy". RSC Advances 6, n.º 10 (2016): 8243–47. http://dx.doi.org/10.1039/c5ra25103f.
Texto completoRocco, Daniele, Isabella Chiarotto, Leonardo Mattiello, Fabiana Pandolfi, Daniela Zane y Marta Feroci. "Electrochemical synthesis and amidation of benzoin: benzamides from benzaldehydes". Pure and Applied Chemistry 91, n.º 10 (25 de octubre de 2019): 1709–15. http://dx.doi.org/10.1515/pac-2018-1118.
Texto completoXia, Ji-Bao, Yan-Lin Li y Zheng-Yang Gu. "Transition-Metal-Catalyzed Intermolecular C–H Carbonylation toward Amides". Synlett 32, n.º 01 (17 de agosto de 2020): 07–13. http://dx.doi.org/10.1055/s-0040-1706416.
Texto completoMkhonazi, Blessing D., Malibongwe Shandu, Ronewa Tshinavhe, Sandile B. Simelane y Paseka T. Moshapo. "Solvent-Free Iron(III) Chloride-Catalyzed Direct Amidation of Esters". Molecules 25, n.º 5 (26 de febrero de 2020): 1040. http://dx.doi.org/10.3390/molecules25051040.
Texto completoPaggiola, Giulia, Nolwenn Derrien, Jonathan D. Moseley, Anthony Green, Sabine L. Flitsch, James H. Clark, Con Robert McElroy y Andrew J. Hunt. "Application of bio-based solvents for biocatalysed synthesis of amides with Pseudomonas stutzeri lipase (PSL)". Pure and Applied Chemistry 92, n.º 4 (28 de abril de 2020): 579–86. http://dx.doi.org/10.1515/pac-2019-0808.
Texto completoBelousov, Artem S., Anton L. Esipovich, Evgeny A. Kanakov y Ksenia V. Otopkova. "Recent advances in sustainable production and catalytic transformations of fatty acid methyl esters". Sustainable Energy & Fuels 5, n.º 18 (2021): 4512–45. http://dx.doi.org/10.1039/d1se00830g.
Texto completoKurouchi, Hiroaki. "Diprotonative stabilization of ring-opened carbocationic intermediates: conversion of tetrahydroisoquinoline to triarylmethanes". Chemical Communications 56, n.º 59 (2020): 8313–16. http://dx.doi.org/10.1039/d0cc01969k.
Texto completoMahato, Sachinta, Sougata Santra, Grigory V. Zyryanov y Adinath Majee. "Metal-Free Amidation Reactions of Terminal Alkynes with Benzenesulfonamide". Journal of Organic Chemistry 84, n.º 6 (26 de febrero de 2019): 3176–83. http://dx.doi.org/10.1021/acs.joc.8b03065.
Texto completoLiu, Bingxian, Bin Li y Baiquan Wang. "Ru(ii)-catalyzed amidation reactions of 8-methylquinolines with azides via C(sp3)–H activation". Chemical Communications 51, n.º 91 (2015): 16334–37. http://dx.doi.org/10.1039/c5cc06230f.
Texto completoWang, Chao, Lingling Huang, Min Lu, Bei Zhao, Yaorong Wang, Yong Zhang, Qi Shen y Yingming Yao. "Anionic phenoxy-amido rare-earth complexes as efficient catalysts for amidation of aldehydes with amines". RSC Adv. 5, n.º 115 (2015): 94768–75. http://dx.doi.org/10.1039/c5ra20285j.
Texto completoLi, C., C. D. Oldham y S. W. May. "NN-dimethyl-1,4-phenylenediamine as an alternative reductant for peptidylglycine α-amidating mono-oxygenase catalysis". Biochemical Journal 300, n.º 1 (15 de mayo de 1994): 31–36. http://dx.doi.org/10.1042/bj3000031.
Texto completoKasahara, Takahito y Marco A. Ciufolini. "Further studies toward himandrine via sequential oxidative amidation – intramolecular Diels–Alder reactions". Canadian Journal of Chemistry 91, n.º 1 (enero de 2013): 82–90. http://dx.doi.org/10.1139/cjc-2012-0340.
Texto completoBera, Shyamal Kanti, Rosalin Bhanja y Prasenjit Mal. "DDQ in mechanochemical C–N coupling reactions". Beilstein Journal of Organic Chemistry 18 (1 de junio de 2022): 639–46. http://dx.doi.org/10.3762/bjoc.18.64.
Texto completoMOORE, Allison B. y Sheldon W. MAY. "Kinetic and inhibition studies on substrate channelling in the bifunctional enzyme catalysing C-terminal amidation". Biochemical Journal 341, n.º 1 (24 de junio de 1999): 33–40. http://dx.doi.org/10.1042/bj3410033.
Texto completoChen, Mei-Lan, Jian-Qing Min, Sheng-Dong Pan y Mi-Cong Jin. "Surface core–shell magnetic polymer modified graphene oxide-based material for 2,4,6-trichlorophenol removal". RSC Advances 4, n.º 108 (2014): 63494–501. http://dx.doi.org/10.1039/c4ra14150d.
Texto completoWang, Danfeng, Hai Huang y Xiaolin Zhu. "Development of anthrazoline photocatalysts for promoting amination and amidation reactions". Chemical Communications 58, n.º 21 (2022): 3529–32. http://dx.doi.org/10.1039/d1cc07315j.
Texto completoHernández, José G., Karen J. Ardila-Fierro, Dajana Barišić y Hervé Geneste. "Multi-faceted reactivity of N-fluorobenzenesulfonimide (NFSI) under mechanochemical conditions: fluorination, fluorodemethylation, sulfonylation, and amidation reactions". Beilstein Journal of Organic Chemistry 18 (7 de febrero de 2022): 182–89. http://dx.doi.org/10.3762/bjoc.18.20.
Texto completoYoshino, Tatsuhiko y Shigeki Matsunaga. "Cp*CoIII-Catalyzed C–H Functionalization and Asymmetric Reactions Using External Chiral Sources". Synlett 30, n.º 12 (7 de mayo de 2019): 1384–400. http://dx.doi.org/10.1055/s-0037-1611814.
Texto completoMartin, Stephen F., Michael P. Dwyer y Christopher L. Lynch. "Application of AlMe3-mediated amidation reactions to solution phase peptide synthesis". Tetrahedron Letters 39, n.º 12 (marzo de 1998): 1517–20. http://dx.doi.org/10.1016/s0040-4039(98)00071-9.
Texto completoGaniek, Maximilian A., Matthias R. Becker, Guillaume Berionni, Hendrik Zipse y Paul Knochel. "Barbier Continuous Flow Preparation and Reactions of Carbamoyllithiums for Nucleophilic Amidation". Chemistry – A European Journal 23, n.º 43 (17 de julio de 2017): 10280–84. http://dx.doi.org/10.1002/chem.201702593.
Texto completoLamani, Manjunath y Kandikere Ramaiah Prabhu. "NIS-Catalyzed Reactions: Amidation of Acetophenones and Oxidative Amination of Propiophenones". Chemistry - A European Journal 18, n.º 46 (5 de octubre de 2012): 14638–42. http://dx.doi.org/10.1002/chem.201202703.
Texto completoCho, Inha, Zhi-Jun Jia y Frances H. Arnold. "Site-selective enzymatic C‒H amidation for synthesis of diverse lactams". Science 364, n.º 6440 (9 de mayo de 2019): 575–78. http://dx.doi.org/10.1126/science.aaw9068.
Texto completoVázquez, Ester y Maurizio Prato. "Functionalization of carbon nanotubes for applications in materials science and nanomedicine". Pure and Applied Chemistry 82, n.º 4 (13 de marzo de 2010): 853–61. http://dx.doi.org/10.1351/pac-con-09-10-40.
Texto completoGoodreid, Jordan D., Petar A. Duspara, Caroline Bosch y Robert A. Batey. "Amidation Reactions from the Direct Coupling of Metal Carboxylate Salts with Amines". Journal of Organic Chemistry 79, n.º 3 (13 de enero de 2014): 943–54. http://dx.doi.org/10.1021/jo402374c.
Texto completoChou, Wen-Chih, Ming-Chen Chou, Yann-Yu Lu y Shyh-Fong Chen. "HMDS-promotedin situ amidation reactions of car☐ylic acids and amines". Tetrahedron Letters 40, n.º 17 (abril de 1999): 3419–22. http://dx.doi.org/10.1016/s0040-4039(99)00505-5.
Texto completoBarfoot, 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, n.º 20 (mayo de 2010): 2685–89. http://dx.doi.org/10.1016/j.tetlet.2010.03.051.
Texto completoTrumbo, David L. "Polymers based on methyl acrylamidoglycolate methyl ether (MAGME): Michael addition-amidation reactions". Polymer Bulletin 31, n.º 5 (noviembre de 1993): 523–29. http://dx.doi.org/10.1007/bf00297887.
Texto completoNguyen, Thanh V. y Demelza J. M. Lyons. "A novel aromatic carbocation-based coupling reagent for esterification and amidation reactions". Chemical Communications 51, n.º 15 (2015): 3131–34. http://dx.doi.org/10.1039/c4cc09539a.
Texto completoRajabi, Fatemeh, Mojdeh Raessi, Rick A. D. Arancon, Mohammad Reza Saidi y Rafael Luque. "Supported cobalt oxide nanoparticles as efficient catalyst in esterification and amidation reactions". Catalysis Communications 59 (enero de 2015): 122–26. http://dx.doi.org/10.1016/j.catcom.2014.09.044.
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