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Search for "organic carbonates" in Full Text gives 6 result(s) in Beilstein Journal of Organic Chemistry.

Valorisation of plastic waste via metal-catalysed depolymerisation

  • Francesca Liguori,
  • Carmen Moreno-Marrodán and
  • Pierluigi Barbaro

Beilstein J. Org. Chem. 2021, 17, 589–621, doi:10.3762/bjoc.17.53

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Published 02 Mar 2021

Direct electrochemical generation of organic carbonates by dehydrogenative coupling

  • Tile Gieshoff,
  • Vinh Trieu,
  • Jan Heijl and
  • Siegfried R. Waldvogel

Beilstein J. Org. Chem. 2018, 14, 1578–1582, doi:10.3762/bjoc.14.135

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  • Leverkusen, Germany Covestro NV, Haven 507 - Scheldelaan 420, 2040 Antwerpen, Belgium 10.3762/bjoc.14.135 Abstract Organic carbonates are an important source for polycarbonate synthesis. However, their synthesis generally requires phosgene, sophisticated catalysts, harsh reaction conditions, or other highly
  • ; dehydrogenative coupling; electrochemistry; organic carbonates; Introduction Polycarbonates are high-performance polymeric materials with versatile applications in various fields with economic impact, e.g., construction, food, and pharmaceutical industry [1]. For their technical large-scale production, organic
  • method for the generation of organic carbonates using inexpensive starting materials without the necessity of catalysts. Generally, alcohols serve as starting materials for the DPC and DMC synthesis. However, efficiency increases if non-functionalized aromatic compounds serve as feedstock. Boron-doped
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Published 27 Jun 2018

Hyper-reticulated calixarene polymers: a new example of entirely synthetic nanosponge materials

  • Alberto Spinella,
  • Marco Russo,
  • Antonella Di Vincenzo,
  • Delia Chillura Martino and
  • Paolo Lo Meo

Beilstein J. Org. Chem. 2018, 14, 1498–1507, doi:10.3762/bjoc.14.127

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  • electrophiles such as epichlorohydrin [6], organic carbonates [7][8][9] or bis-isocyanates [10], in variable ratios depending on the required degree of reticulation. The process, of course, exploits the nucleophilic reactivity of the hydroxy groups of the macrocycle oligosaccharide unit. In general, CyNSs
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Published 20 Jun 2018

Isosorbide and dimethyl carbonate: a green match

  • Fabio Aricò and
  • Pietro Tundo

Beilstein J. Org. Chem. 2016, 12, 2256–2266, doi:10.3762/bjoc.12.218

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  • presence of the nitrogen bicyclic base DBU. It has been, in fact, reported that organic carbonates are activated by DBU via formation of an N-alkoxycarbonyl DBU derivative [67][68][69][70][71]. However, in this case study, DBU most probably promotes the formation of the methoxycarbonyl reaction
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Published 26 Oct 2016

Ionic liquids as transesterification catalysts: applications for the synthesis of linear and cyclic organic carbonates

  • Maurizio Selva,
  • Alvise Perosa,
  • Sandro Guidi and
  • Lisa Cattelan

Beilstein J. Org. Chem. 2016, 12, 1911–1924, doi:10.3762/bjoc.12.181

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  • /nucleophilic) activation of reactants. Keywords: ionic liquids; transesterification; organocatalysts; organic carbonates; Review Introduction Transesterification catalysts The transesterification is one of the classical organic reactions that has found numerous applications in laboratory practice as well as
  • homogeneous catalytic systems for transesterification reactions. Remarkable examples are those of triethylamine (TEA) and Fe–Zn double-metal cyanide complexes [20][21]. Among other applications, these compounds successfully catalyzed the reaction of DMC and other organic carbonates with polyols (e.g
  • transesterification reaction for the synthesis of organic carbonates Organic carbonates (OCs) are promising candidates as green replacements of conventional noxious solvents and fuel additives as well as for the development of innovative intermediates in the pharma, lubricant and polymer industries [55][56]. Before
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Published 26 Aug 2016

Surprisingly facile CO2 insertion into cobalt alkoxide bonds: A theoretical investigation

  • Willem K. Offermans,
  • Claudia Bizzarri,
  • Walter Leitner and
  • Thomas E. Müller

Beilstein J. Org. Chem. 2015, 11, 1340–1351, doi:10.3762/bjoc.11.144

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  • ]. Even so, industrial processes using CO2 as chemical feedstock are limited to the production of few large scale chemicals such as urea, methanol, salicylic acid as well as inorganic and organic carbonates [5]. Since CO2 is captured in huge amounts from the flue gases of fossil fuel combustion, it would
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Published 31 Jul 2015
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