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Carbohydr Polym Special Issue Invited contribution: Click chemistry for block polysaccharides with dihydrazide and dioxyamine linkers - A review.
Solberg, Amalie; Mo, Ingrid V; Omtvedt, Line Aa; Strand, Berit L; Aachmann, Finn L; Schatz, Christophe; Christensen, Bjørn E.
Afiliação
  • Solberg A; NOBIPOL, Department of Biotechnology and Food Science, NTNU Norwegian University of Science and Technology, Sem Sælands vei 6/8, NO-7491 Trondheim, Norway.
  • Mo IV; NOBIPOL, Department of Biotechnology and Food Science, NTNU Norwegian University of Science and Technology, Sem Sælands vei 6/8, NO-7491 Trondheim, Norway.
  • Omtvedt LA; NOBIPOL, Department of Biotechnology and Food Science, NTNU Norwegian University of Science and Technology, Sem Sælands vei 6/8, NO-7491 Trondheim, Norway.
  • Strand BL; NOBIPOL, Department of Biotechnology and Food Science, NTNU Norwegian University of Science and Technology, Sem Sælands vei 6/8, NO-7491 Trondheim, Norway.
  • Aachmann FL; NOBIPOL, Department of Biotechnology and Food Science, NTNU Norwegian University of Science and Technology, Sem Sælands vei 6/8, NO-7491 Trondheim, Norway.
  • Schatz C; LCPO, Université de Bordeaux, UMR 5629, ENSCBP, 16, Avenue Pey Berland, 33607 Pessac Cedex, France. Electronic address: schatz@enscbp.fr.
  • Christensen BE; NOBIPOL, Department of Biotechnology and Food Science, NTNU Norwegian University of Science and Technology, Sem Sælands vei 6/8, NO-7491 Trondheim, Norway. Electronic address: bjorn.e.christensen@ntnu.no.
Carbohydr Polym ; 278: 118840, 2022 Feb 15.
Article em En | MEDLINE | ID: mdl-34973722
Engineered block polysaccharides is a relatively new class of biomacromolecules consisting of chemical assembly of separate block structures at the chain termini. In contrast to conventional, laterally substituted polysaccharide derivatives, the block arrangement allows for much higher preservation of inherent chain properties such as biodegradability and stimuli-responsive self-assembly, while at the same time inducing new macromolecular properties. Abundant, carbon neutral, and even recalcitrant biomass is an excellent source of blocks, opening for numerous new uses of biomass for a wide range of novel biomaterials. Among a limited range of methodologies available for block conjugation, bifunctional linkers allowing for oxyamine and hydrazide 'click' reactions have recently proven useful additions to the repertoire. This article focuses the chemistry and kinetics of these reactions. It also presents some new data with the aim to provide useful protocols and methods for general use towards new block polysaccharides.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Polissacarídeos / Aminas / Hidrazonas Idioma: En Revista: Carbohydr Polym Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Noruega

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Polissacarídeos / Aminas / Hidrazonas Idioma: En Revista: Carbohydr Polym Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Noruega