Relevant bibliographies by topics / Aminolyse de lactone

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters

Academic literature on the topic 'Aminolyse de lactone'

Author: Grafiati
Published: 4 June 2021
Last updated: 7 February 2022

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Journal articles on the topic "Aminolyse de lactone"

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Pongracz, 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 (2021): 157–66. http://dx.doi.org/10.1007/s10719-020-09971-7.

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AbstractSialic acids occur ubiquitously throughout vertebrate glycomes and often endcap glycans in either α2,3- or α2,6-linkage with diverse biological roles. Linkage-specific sialic acid characterization is increasingly performed by mass spectrometry, aided by differential sialic acid derivatization to discriminate between linkage isomers. Typically, during the first step of such derivatization reactions, in the presence of a carboxyl group activator and a catalyst, α2,3-linked sialic acids condense with the subterminal monosaccharides to form lactones, while α2,6-linked sialic acids form ami
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Mercado-Marin, Eduardo V., Pratik Rajesh Chheda, Andrea Faulkner, and Diane Carrera. "Magnesium ethoxide mediated lactone aminolysis with aminoheterocycles." Tetrahedron Letters 61, no. 9 (2020): 151552. http://dx.doi.org/10.1016/j.tetlet.2019.151552.

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Jeznach, Oliwia, Dorota Kolbuk, and Paweł Sajkiewicz. "Aminolysis of Various Aliphatic Polyesters in a Form of Nanofibers and Films." Polymers 11, no. 10 (2019): 1669. http://dx.doi.org/10.3390/polym11101669.

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Surface functionalization of polymer scaffolds is a method used to improve interactions of materials with cells. A frequently used method for polyesters is aminolysis reaction, which introduces free amine groups on the surface. In this study, nanofibrous scaffolds and films of three different polyesters–polycaprolactone (PCL), poly(lactide-co-caprolactone) (PLCL), and poly(l-lactide) (PLLA) were subjected to this type of surface modification under the same conditions. Efficiency of aminolysis was evaluated on the basis of ninhydrin tests and ATR–FTIR spectroscopy. Also, impact of this treatmen
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Bakry, Ahmed, Mohamed S. A. Darwish, and Ahmed M. A. El Naggar. "Assembling of hydrophilic and cytocompatible three-dimensional scaffolds based on aminolyzed poly(l-lactide) single crystals." New Journal of Chemistry 42, no. 20 (2018): 16930–39. http://dx.doi.org/10.1039/c8nj03205j.

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Matsumoto, Kiyoshi, Shiro Hashimoto, Takane Uchida, Tadashi Okamoto, and Shinichi Otani. "High-Pressure Aminolysis of Lactones to Hydroxy Amides." Bulletin of the Chemical Society of Japan 62, no. 10 (1989): 3138–42. http://dx.doi.org/10.1246/bcsj.62.3138.

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Bertucci, Michael A., Stephen J. Lee, and Michel R. Gagné. "Thiourea-catalyzed aminolysis of N-acyl homoserine lactones." Chemical Communications 49, no. 20 (2013): 2055. http://dx.doi.org/10.1039/c3cc00268c.

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Foley, Megan A., and Timothy F. Jamison. "Amide Bond Formation via Reversible, Carboxylic Acid-Promoted Lactone Aminolysis." Organic Process Research & Development 14, no. 5 (2010): 1177–81. http://dx.doi.org/10.1021/op1001269.

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Liu, Wenming, David D. Xu, Oljan Repič, and Thomas J. Blacklock. "A mild method for ring-opening aminolysis of lactones." Tetrahedron Letters 42, no. 13 (2001): 2439–41. http://dx.doi.org/10.1016/s0040-4039(01)00196-4.

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Blay, Gonzalo, Luz Cardona, Begoña García, Cristina L. García, and José R. Pedro. "A non-catalyzed ring-opening aminolysis reaction of sesquiterpene lactones." Tetrahedron Letters 35, no. 6 (1994): 931–34. http://dx.doi.org/10.1016/s0040-4039(00)76003-5.

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Hoagland, Peter D., Helmut Pessen, and George G. Mcdonald. "The Formation of Intermediate Lactones During Aminolysis of Diethyl Xylarate." Journal of Carbohydrate Chemistry 6, no. 3 (1987): 495–99. http://dx.doi.org/10.1080/07328308708057936.

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Dissertations / Theses on the topic "Aminolyse de lactone"

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Durel, Vianney. "Développements méthodologiques de la cyclisation d’aza-Prins et aminolyse de lactone pour la synthèse de nouvelles structures peptidomimétiques- pipéridines." Thesis, Rennes 1, 2016. http://www.theses.fr/2016REN1S100/document.

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Les tétrahydropyranes et les pipéridines sont des motifs que l'on retrouve dans de nombreuses molécules naturelles bioactives. L'intérêt pour ces familles de composés ne cesse de croître. En effet le noyau pipéridine est le troisième motif cyclique le plus retrouvé dans les molécules thérapeutiques après les noyaux phényle et pyridine alors que le tétrahydropyrane prend lui la 6ème place. Il apparaît donc opportun de développer des voies d'accès simples et efficaces afin d'obtenir de façon stéréosélective (diastéréo et/ou énantiosélective) ces motifs structuraux. Les travaux de recherche prése
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AL, TARAKJI YOUSSR. "Synthese des modeles de metabolites de medicaments de la serie du glutethimide et etude de reactions d'alcoolyse-aminolyse se produisant au cours du metabolisme (doctorat : pharmacochimie)." Paris 11, 1999. http://www.theses.fr/1999PA114837.

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Book chapters on the topic "Aminolyse de lactone"

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Ziegler, T. "Aminolysis of Acylboranes." In Three Carbon-Heteroatom Bonds: Esters and Lactones; Peroxy Acids and R(CO)OX Compounds; R(CO)X, X=S, Se, Te. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-021-00022.

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Ziegler, T. "By Aminolysis with Amines or Metal Amides." In Three Carbon-Heteroatom Bonds: Esters and Lactones; Peroxy Acids and R(CO)OX Compounds; R(CO)X, X=S, Se, Te. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-021-00036.

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Li, W.-R. "Aluminum Trichloride Promoted Aminolysis of Cyclic Imides." In Three Carbon-Heteroatom Bonds: Esters and Lactones; Peroxy Acids and R(CO)OX Compounds; R(CO)X, X=S, Se, Te. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-021-00158.

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You might also be interested in the extended bibliographies on the topic 'Aminolyse de lactone' for particular source types:
Journal articles
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