Literature DB >> 22213713

Isosorbide as a renewable platform chemical for versatile applications--quo vadis?

Marcus Rose1, Regina Palkovits.   

Abstract

Isosorbide is a platform chemical of considerable importance for the future replacement of fossil resource-based products. Applications as monomers and building blocks for new polymers and functional materials, new organic solvents, for medical and pharmaceutical applications, and even as fuels or fuel additives are conceivable. The conversion of isosorbide to valuable derivatives by functionalization or substitution of the hydroxyl groups is difficult because of the different configurations of the 2- and 5-positions and the resulting different reactivity and steric hindrance of the two hydroxyl groups. Although a substantial amount of work has been published using exclusively the endo or exo derivatives isomannide and isoidide, respectively, as starting material, a considerable effort is still necessary to transfer and adapt these methods for the efficient conversion of isosorbide. This Minireview deals with all aspects of isosorbide chemistry, which includes its production by catalytic processes, special properties, and chemical transformations for its utilization in biogenic polymers and other applications of interest.
Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Year:  2011        PMID: 22213713     DOI: 10.1002/cssc.201100580

Source DB:  PubMed          Journal:  ChemSusChem        ISSN: 1864-5631            Impact factor:   8.928


  19 in total

1.  Chemoselective conversion of biologically sourced polyols into chiral synthons.

Authors:  Laura L Adduci; Trandon A Bender; Jennifer A Dabrowski; Michel R Gagné
Journal:  Nat Chem       Date:  2015-07       Impact factor: 24.427

2.  An Overview of Biorefinery Derived Platform Chemicals from a Cellulose and Hemicellulose Biorefinery.

Authors:  Sudhakar Takkellapati; Tao Li; Michael A Gonzalez
Journal:  Clean Technol Environ Policy       Date:  2018-09       Impact factor: 3.636

3.  Hydrophobically Modified Isosorbide Dimethacrylates as a Bisphenol-A (BPA)-Free Dental Filling Material.

Authors:  Bilal Marie; Raymond Clark; Tim Gillece; Seher Ozkan; Michael Jaffe; Nuggehalli M Ravindra
Journal:  Materials (Basel)       Date:  2021-04-22       Impact factor: 3.623

4.  Transition metal triflate catalyzed conversion of alcohols, ethers and esters to olefins.

Authors:  J Keskiväli; A Parviainen; K Lagerblom; T Repo
Journal:  RSC Adv       Date:  2018-04-23       Impact factor: 3.361

Review 5.  Isosorbide and dimethyl carbonate: a green match.

Authors:  Fabio Aricò; Pietro Tundo
Journal:  Beilstein J Org Chem       Date:  2016-10-26       Impact factor: 2.883

6.  Fluoride-promoted carbonylation polymerization: a facile step-growth technique to polycarbonates.

Authors:  J V Olsson; D Hult; S García-Gallego; M Malkoch
Journal:  Chem Sci       Date:  2017-05-04       Impact factor: 9.825

7.  New biosourced AA and AB monomers from 1,4:3,6-dianhydrohexitols, Isosorbide, Isomannide, and Isoidide.

Authors:  Asma Saadaoui; Raouf Medimagh; Sylvain Marque; Damien Prim; Saber Chatti; Herve Casabianca; Mongia Said Zina
Journal:  Des Monomers Polym       Date:  2016-10-23       Impact factor: 2.650

8.  Microwave-assisted synthesis of isosorbide-derived diols for the preparation of thermally stable thermoplastic polyurethane.

Authors:  Nejib Kasmi; Martina Roso; Nadia Hammami; Mustapha Majdoub; Carlo Boaretti; Paolo Sgarbossa; Chiara Vianello; Giuseppe Maschio; Michele Modesti; Alessandra Lorenzetti
Journal:  Des Monomers Polym       Date:  2017-11-13       Impact factor: 2.650

Review 9.  One-pot synthesis of isosorbide from cellulose or lignocellulosic biomass: a challenge?

Authors:  Isaline Bonnin; Raphaël Mereau; Thierry Tassaing; Karine De Oliveira Vigier
Journal:  Beilstein J Org Chem       Date:  2020-07-16       Impact factor: 2.883

10.  From D-sorbitol to five-membered bis(cyclo-carbonate) as a platform molecule for the synthesis of different original biobased chemicals and polymers.

Authors:  Pierre Furtwengler; Luc Avérous
Journal:  Sci Rep       Date:  2018-06-14       Impact factor: 4.379

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