Literature DB >> 28445630

Murai Reaction on Furfural Derivatives Enabled by Removable N,N'-Bidentate Directing Groups.

Cristofer Pezzetta1, Luis F Veiros2, Julie Oble1, Giovanni Poli1.   

Abstract

Furfural and related compounds are industrially relevant building blocks obtained from lignocellulosic biomass. To enhance the added value of these renewable resources, a Ru-catalyzed hydrofurylation of alkenes, involving a directed C-H activation at C3 of the furan ring, was developed. A thorough experimental study revealed that a bidentate amino-imine directing group enabled the desired coupling. Removal of the directing group occurred during the purification step, directly releasing the C3-functionalized furfurals. Development of the reaction as well as optimization and scope of the method were described. A mechanism was proposed on the basis of DFT calculations.
© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  C−H activation; aldimines; alkenes; furfural; ruthenium

Year:  2017        PMID: 28445630     DOI: 10.1002/chem.201701850

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  2 in total

1.  Modular synthesis of 2-furyl carbinols from 3-benzyldimethylsilylfurfural platforms relying on oxygen-assisted C-Si bond functionalization.

Authors:  Sebastien Curpanen; Per Reichert; Gabriele Lupidi; Giovanni Poli; Julie Oble; Alejandro Perez-Luna
Journal:  Beilstein J Org Chem       Date:  2022-09-16       Impact factor: 2.544

Review 2.  The Increasing Value of Biomass: Moving From C6 Carbohydrates to Multifunctionalized Building Blocks via 5-(hydroxymethyl)furfural.

Authors:  Konstantin I Galkin; Valentine P Ananikov
Journal:  ChemistryOpen       Date:  2020-11-06       Impact factor: 2.630

  2 in total

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