Relevant bibliographies by topics / Isohexide

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  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic 'Isohexide'

Author: Grafiati
Published: 6 September 2023
Last updated: 31 July 2025

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Journal articles on the topic "Isohexide"

1

Wroblewska, Aleksandra, Arkadiusz Zych, Shanmugam Thiyagarajan, et al. "Towards sugar-derived polyamides as environmentally friendly materials." Polymer Chemistry 6, no. 22 (2015): 4133–43. http://dx.doi.org/10.1039/c5py00521c.

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As part of our ongoing study investigating isohexide-based polyamides, we have synthesized isosorbide(bis(propan-1-amine)) (DAPIS) and studied its reactivity in the polymerization towards fully biobased polyamides.
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Marubayashi, Hironori, Takaaki Ushio, and Shuichi Nojima. "Crystallization of polyesters composed of isohexides and aliphatic dicarboxylic acids: Effects of isohexide stereoisomerism and dicarboxylic acid chain length." Polymer Degradation and Stability 146 (December 2017): 174–83. http://dx.doi.org/10.1016/j.polymdegradstab.2017.10.005.

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3

Ji, Xiaodong, Zikun Wang, Jingling Yan, and Zhen Wang. "Partially bio-based polyimides from isohexide-derived diamines." Polymer 74 (September 2015): 38–45. http://dx.doi.org/10.1016/j.polymer.2015.07.051.

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4

Wu, Jing, Pieter Eduard, Shanmugam Thiyagarajan, et al. "Isohexide Derivatives from Renewable Resources as Chiral Building Blocks." ChemSusChem 4, no. 5 (2011): 599–603. http://dx.doi.org/10.1002/cssc.201100076.

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5

Wu, Jing, Shanmugam Thiyagarajan, Célia Fonseca Guerra, et al. "Isohexide Dinitriles: A Versatile Family of Renewable Platform Chemicals." ChemSusChem 10, no. 16 (2017): 3202–11. http://dx.doi.org/10.1002/cssc.201700617.

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Rajput, Bhausaheb S., Kalpakasseril Girija Lekshmy, Shamal K. Menon, and Samir H. Chikkali. "Synthesis of isohexide-di(ether-ene)s and ADMET polymerization." Green Materials 5, no. 2 (2017): 63–73. http://dx.doi.org/10.1680/jgrma.16.00017.

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7

Wu, Jing, Jiefei Qi, Yiming Lin, et al. "Lipase-Catalyzed Fully Aliphatic Copolyesters Based on Renewable Isohexide Isomers." ACS Sustainable Chemistry & Engineering 9, no. 4 (2021): 1599–612. http://dx.doi.org/10.1021/acssuschemeng.0c06733.

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8

Wu, Jing, Pieter Eduard, Lidia Jasinska-Walc, et al. "Fully Isohexide-Based Polyesters: Synthesis, Characterization, and Structure–Properties Relations." Macromolecules 46, no. 2 (2012): 384–94. http://dx.doi.org/10.1021/ma302209f.

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9

Gormong, Ethan A., Theresa M. Reineke, and Thomas R. Hoye. "Synthesis of Isohexide Diyne Polymers and Hydrogenation to Their Saturated Polyethers." ACS Macro Letters 10, no. 8 (2021): 1068–72. http://dx.doi.org/10.1021/acsmacrolett.1c00422.

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10

Ji, Xiaodong, Zikun Wang, Zhen Wang, and Jingling Yan. "Bio-Based Poly(Ether Imide)s from Isohexide-Derived Isomeric Dianhydrides." Polymers 9, no. 11 (2017): 569. http://dx.doi.org/10.3390/polym9110569.

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Dissertations / Theses on the topic "Isohexide"

1

Rajput, B. S. "Isohexide and plant oil based renewable and degradable polymers." Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 2019. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/5859.

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Rajput, Bhausaheb. "Isohexide and plant oil based renewable and degradable polymers." Thesis(PhD), CSIR - National Chemical Laboratory, Pune, 2019. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/5829.

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The thesis titled “Isohexide and Plant Oil Based Renewable and Degradable Polymers” is divided into six chapters. Chapter-1 deals with the detailed literature survey on the use of sugar based isohexides (isomannide 1a, isosorbide 1b and isoidide 1c) and plant oil based diols for the synthesis of various renewable and degradable polymers.1 Chapter-2 describes the synthesis of sugar based isohexide-diacetals and their polymerization to corresponding degradable polyacetals. Chapter-3 deals with the synthesis of renewable copolyacetals from sugar based isohexide-diacetals and plant oil based long
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3

Janvier, Marine. "Les isohexides comme nouvelle plateforme biosourcée pour l’organocatalyse." Thesis, Lyon 1, 2015. http://www.theses.fr/2015LYO10223/document.

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L'isosorbide est un dianhydrohexitol chiral obtenu énantiomériquement pur par double déshydratation du sorbitol, un des produits majoritaires de l'industrie amidonnière résultant de l'hydrogénation du glucose. L'intérêt croissant pour l'isosorbide ces deux dernières décennies s'explique notamment grâce à sa production industrielle par des entreprises comme Roquette (20 000 tonnes par an). Cette disponibilité a permis la valorisation de l isosorbide dans divers domaines : polymères (polyéthylène isosorbide téréphtalate), tensioactifs, solvants (diméthyl isosorbide) et pharmaceutique (isosorbide
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Engel, Rebecca [Verfasser], Regina [Akademischer Betreuer] Palkovits, and Carsten [Akademischer Betreuer] Bolm. "Heterogeneously catalysed amination and isomerisation of isohexides / Rebecca Veronika Engel ; Regina Palkovits, Carsten Bolm." Aachen : Universitätsbibliothek der RWTH Aachen, 2016. http://d-nb.info/1130590240/34.

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Engel, Rebecca Veronika Verfasser], Regina [Akademischer Betreuer] [Palkovits, and Carsten [Akademischer Betreuer] Bolm. "Heterogeneously catalysed amination and isomerisation of isohexides / Rebecca Veronika Engel ; Regina Palkovits, Carsten Bolm." Aachen : Universitätsbibliothek der RWTH Aachen, 2016. http://d-nb.info/1130590240/34.

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6

Kadraoui, Mohammed. "Design et utilisations de complexes organométalliques intercalés dans la bentonite pour des réactions d’insertion ou de complexes organométalliques chiraux pour des réactions de cyclopropanation asymétrique." Thesis, Le Mans, 2015. http://www.theses.fr/2015LEMA1026.

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Cette thèse est constituée de deux parties indépendantes. La première consiste à former de nouveaux systèmes catalytiques hétérogènes par intercalation d’éthylacétonate de cuivre et de fer dans une argile : la bentonite. Pour cela, celle-ci est purifiée avant d’inclure les deux complexes. Une étude de l’activité de ces deux matériaux a été réalisée avec le diazoacétate d’éthyle afin de former le fumarate et le maléate d’éthyle. Des réactions d’insertion de carbènes ont ensuite été étudiées avec des amines et des alcools en vue de former respectivement des a-oxa et a-aza acétates d’éthyles avec
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