Literature DB >> 27809503

Biobased Amines: From Synthesis to Polymers; Present and Future.

Vincent Froidevaux1, Claire Negrell1, Sylvain Caillol1, Jean-Pierre Pascault2,3, Bernard Boutevin1.   

Abstract

Amines are key intermediates in the chemical industry due to their nucleophilic characteristic which confers a high reactivity to them. Thus, they are key monomers for the synthesis of polyamides, polyureas, polyepoxydes, which are all of growing interest in automotive, aerospace, building, or health applications. Despite a growing interest for biobased monomers and polymers, and particularly polyamides, it should be noticed that very few natural amines are available. Actually, there is only chitosan and poly(lysine). In this review we present both fundamental and applied research on the synthesis of biobased primary and secondary amines with current available biobased resources. Their use is described as a building block for material chemistry. Hence, we first recall some background on the synthesis of amines, including the reactivity of amines. Second we focus on the synthesis of biobased amines from all sorts of biomass, from carbohydrate, terpenes, or oleochemical sources. Third, because they need optimization and technological developments, we discuss some examples of their use for the creation of biobased polymers. We conclude with the future of the synthesis of biobased amines and their use in different applications.

Entities:  

Year:  2016        PMID: 27809503     DOI: 10.1021/acs.chemrev.6b00486

Source DB:  PubMed          Journal:  Chem Rev        ISSN: 0009-2665            Impact factor:   60.622


  29 in total

1.  Rearrangement of Benzylic Trichloroacetimidates to Benzylic Trichloroacetamides.

Authors:  Arijit A Adhikari; Tamie Suzuki; Reesheda T Gilbert; Matthew R Linaburg; John D Chisholm
Journal:  J Org Chem       Date:  2017-03-27       Impact factor: 4.354

2.  A General N-alkylation Platform via Copper Metallaphotoredox and Silyl Radical Activation of Alkyl Halides.

Authors:  Nathan W Dow; Albert Cabré; David W C MacMillan
Journal:  Chem       Date:  2021-06-16       Impact factor: 25.832

3.  Efficient and scalable synthesis of 1,5-diamino-2-hydroxy-pentane from L-lysine via cascade catalysis using engineered Escherichia coli.

Authors:  Yangyang Li; Alei Zhang; Shewei Hu; Kequan Chen; Pingkai Ouyang
Journal:  Microb Cell Fact       Date:  2022-07-16       Impact factor: 6.352

Review 4.  Physical and Chemical Factors Influencing the Printability of Hydrogel-based Extrusion Bioinks.

Authors:  Sang Cheon Lee; Gregory Gillispie; Peter Prim; Sang Jin Lee
Journal:  Chem Rev       Date:  2020-08-20       Impact factor: 60.622

5.  Synthesis of a tyrosinase inhibitor by consecutive ethenolysis and cross-metathesis of crude cashew nutshell liquid.

Authors:  Jacqueline Pollini; Valentina Bragoni; Lukas J Gooßen
Journal:  Beilstein J Org Chem       Date:  2018-10-31       Impact factor: 2.883

6.  Facile Chemical Access to Biologically Active Norcantharidin Derivatives from Biomass.

Authors:  Konstantin I Galkin; Fedor A Kucherov; Oleg N Markov; Ksenia S Egorova; Alexandra V Posvyatenko; Valentine P Ananikov
Journal:  Molecules       Date:  2017-12-12       Impact factor: 4.411

7.  Solvent-Free Method for the Copolymerization of Labile Sugar-Derived Building Blocks into Polyamides.

Authors:  Aleksandra A Wróblewska; Sander Stevens; Wessel Garsten; Stefaan M A De Wildeman; Katrien V Bernaerts
Journal:  ACS Sustain Chem Eng       Date:  2018-09-07       Impact factor: 8.198

8.  Phosphite mediated asymmetric N to C migration for the synthesis of chiral heterocycles from primary amines.

Authors:  Soniya Rani; Soumya Ranjan Dash; Asish Bera; Md Nirshad Alam; Kumar Vanka; Pradip Maity
Journal:  Chem Sci       Date:  2021-05-28       Impact factor: 9.825

9.  Enzymatic Polymerization of Dimethyl 2,5-Furandicarboxylate and Heteroatom Diamines.

Authors:  Dina Maniar; Katharina F Hohmann; Yi Jiang; Albert J J Woortman; Jur van Dijken; Katja Loos
Journal:  ACS Omega       Date:  2018-06-28

10.  Simple ruthenium-catalyzed reductive amination enables the synthesis of a broad range of primary amines.

Authors:  Thirusangumurugan Senthamarai; Kathiravan Murugesan; Jacob Schneidewind; Narayana V Kalevaru; Wolfgang Baumann; Helfried Neumann; Paul C J Kamer; Matthias Beller; Rajenahally V Jagadeesh
Journal:  Nat Commun       Date:  2018-10-08       Impact factor: 14.919

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