100569-46-8Relevant articles and documents
Synthesis and evaluation of D-gluconamides as green mineral scales
Reis, Marcelo I.P.,Gon?alves, Aline D.,Da Silva, Fernando De C.,Jord?o, Alessandro K.,Alves, Ricardo J.,De Andrade, Saulo Fernandes,Resende, Jackson A.L.C.,Rocha, Anderson A.,Ferreira, Vitor F.
, p. 6 - 12 (2012)
A series of 13 d-gluconamides were synthesized in moderate to good yields and evaluated as green scale inhibitors. The crystal structures of two compounds were determined by X-ray crystallography. The compounds 6c and 6d showed a reasonable inhibition of BaSO4 precipitation from aqueous solution (47% and 51%, respectively) that indicated the potential for these derivatives of δ-gluconolactone.
Synthesis of crosslinked nanostructured saccharidic vinyl copolymers and their functionalization
Bertini, Vincenzo,Pocci, Marco,Alfei, Silvana,Idini, Barbara,Lucchesini, Francesco
, p. 11672 - 11680 (2008/03/13)
Saccharidic monomers and a macromonomer were synthesized and copolymerized in the presence of divinylbenzene (DVB) as crosslinker in conditions of separation of phases to give hydrophilic nanostructured sugar-based vinyl copolymers. Appropriate model molecules such as N-benzyl-d-gluconamide for the saccharidic copolymers and 4-(4-chlorobutoxy)benzaldehyde and (E)-4-(4-chloro-2-butenyloxy)benzaldehyde for electrophilic reagents prefiguring possible copper amine oxidase inhibitors allowed identification of conditions for useful monofunctionalizations mainly at the position 2 of the saccharidic units. The examined samples of the nanostructured copolymers from one of the monomers proved to be stable enough to tolerate the functionalization reactions without loss of morphology.
