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Katrin Fridriks

aminolysis of esters

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aminolysis of esters

https://doi.org/10.1038/s41467-019-13326-8, https://doi.org/10.1134/S1070363210050178, https://doi.org/10.1002/9780470166284.ch1, https://doi.org/10.1007/s11176-005-0052-1, https://doi.org/10.1002/jlac.198719870809, https://doi.org/10.1080/00397918608056346, https://doi.org/10.1016/0001-8686(84)80002-0, https://doi.org/10.1016/S0040-4020(01)91244-X, https://doi.org/10.1016/0021-9797(83)90089-9, https://doi.org/10.1016/S0040-4020(01)91865-4, https://doi.org/10.1016/0045-2068(78)90018-4, https://doi.org/10.1016/0040-4020(78)88412-9, https://doi.org/10.1016/0045-2068(75)90008-5, https://doi.org/10.1016/S0022-328X(00)88017-1, https://doi.org/10.1016/S0040-4039(01)98693-9. Reactivity of α-amino acids in the N-acylation with benzoic acid esters in aqueous dioxane. Improved immobilization of gelatin on a modified polyurethane urea. -PHENYLCARBAMATES WITH ANILINE. Theoretical study on the aminolysis of p-substituted phenyl acetates with dimeric ammonia in vacuo and acetonitrile. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Aminolysis of Allyl Esters with Bislithium Aryl Amides. Minah Shin, Min-Young Kim, Ik-Hwan Um. Role of Solvent on Nonenzymatic Peptide Bond Formation Mechanisms and Kinetic Isotope Effects. Evidence of Bifunctional Catalysis. Miroslav A. Rangelov, Georgi N. Vayssilov, Vihra M. Yomtova, Dimiter D. Petkov. Conversion of Ester into Alcohols: Reduction. Theoretical study on the aminolysis of ester catalyzed by TBD: Hydrogen bonding or covalent bonding of the catalyst?. DABCO (DABCO is 1,4-diazobicyclo[2.2.2]octane), referred to as DABAL–Me3.

Information. jo0263723si20021206_124531.pdf (56.04 kb), http://pubs.acs.org/page/copyright/permissions.html, https://doi.org/10.1021/acs.chemrev.8b00712, https://doi.org/10.1021/acs.biomac.8b00322, https://doi.org/10.1021/acs.inorgchem.5b01074, https://doi.org/10.1007/s00214-020-02688-8, https://doi.org/10.1016/j.molliq.2020.112579, https://doi.org/10.1016/j.carres.2019.107821, https://doi.org/10.1016/j.apcatb.2018.01.025, https://doi.org/10.1007/s00214-017-2124-9, https://doi.org/10.1007/s00214-017-2102-2, https://doi.org/10.1007/s00894-016-3084-z, https://doi.org/10.1016/j.comptc.2015.09.022, https://doi.org/10.1007/s00214-015-1634-6, https://doi.org/10.5012/bkcs.2014.35.8.2410, https://doi.org/10.5012/bkcs.2014.35.8.2443, https://doi.org/10.5012/bkcs.2014.35.7.2130, https://doi.org/10.5012/bkcs.2014.35.4.1128, https://doi.org/10.1016/j.comptc.2012.12.018, https://doi.org/10.1007/s11164-012-0517-x, https://doi.org/10.1016/j.molcata.2011.12.003, https://doi.org/10.1016/j.jmgm.2011.05.004, https://doi.org/10.1146/annurev-biochem-082108-165150, https://doi.org/10.1016/j.jmgm.2010.07.006, https://doi.org/10.1016/j.theochem.2009.12.012, https://doi.org/10.1016/j.theochem.2009.04.039, https://doi.org/10.1016/j.tet.2008.07.081, https://doi.org/10.5012/bkcs.2008.29.7.1335, https://doi.org/10.5012/bkcs.2008.29.4.772, https://doi.org/10.1016/j.chemphys.2008.01.036, https://doi.org/10.1080/17415990701490950, https://doi.org/10.1016/j.cplett.2006.06.015, https://doi.org/10.1016/S0166-1280(03)00310-5, https://doi.org/10.4018/978-1-4666-5125-8.ch004, https://doi.org/10.4018/978-1-60960-860-6.ch013. Kinetic Study on Aminolysis of Y-Substituted-Phenyl Picolinates: Effect of H-Bonding Interaction on Reactivity and Transition-State Structure. Stereoselective Synthesis of New Chiral N-Tertiary Tetrasubstituted β-Enamino Ester Piperidines through an Ammonia-Catalyzed Process.

In-depth study on aminolysis of poly(ɛ-caprolactone): Back to the fundamentals. Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Synthesis and Cyclization of Dialkylmalonuric Esters. Computational Study of the Aminolysis of Anhydrides: Effect of the Catalysis to the Reaction of Succinic Anhydride with Methylamine in Gas Phase and Nonpolar Solution. Han-Bing Rao, Yan-Ying Wang, Xian-Yin Zeng, Ying Xue, Ze-Rong Li. Pietro Tundo, F. Aricò, Anthony E. Rosamilia, S. Grego, L. Rossi. A New Polyhydrocarbon−Polyamine AB Block Copolymer. Good diastereoselectivity is observed in the reactions of l-valine or l-isoleucine derived aldehydes catalyzed by a (R)-1-(1-naphthyl)ethylamine derived guanidine. The syn-Oriented 2-OH Provides a Favorable Proton Transfer Geometry in 1,2-Diol Monoester Aminolysis:  Implications for the Ribosome Mechanism. Tetyana Petrova, Sergiy Okovytyy, Leonid Gorb and Jerzy Leszczynski. write an equation to describe the hydrolysis of an ester under acidic or basic conditions.

Takashi Ohshima, Yukiko Hayashi, Kazushi Agura, Yuka Fujii, Asako Yoshiyama, Kazushi Mashima. Mechanism.

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