Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Efficient catalyst reuse by simple dissolution in non-conventional media.

Carlos A M Afonso1, Luís C Branco, Nuno R Candeias

  • 1Departamento de Engenharia Química é Biológica, Instituto Superior Técnico, Complexo 1, Av. Rovisco Pais, 1049-001 Lisboa, Portugal. carlosafonso@ist.utl.pt

Chemical Communications (Cambridge, England)
|June 28, 2007
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Screening of Ionic Liquids and Deep Eutectic Solvents for Enhancing the Activity and Stability of Fungal Laccase: Empowering Kinetic Parameters and Long-Term Conservation.

ACS omega·2026
Same author

Extremotolerant fungi in resinous soils: a unique diversity of generalists and specialized hydrocarbon degraders.

BMC microbiology·2026
Same author

BASHY dyes as modular chromophores for multifaceted biorelevant applications: from imaging to photodynamic therapy.

Chemical communications (Cambridge, England)·2026
Same author

Electrochemical Oxidation of Abietic and Dehydroabietic Acids for Sustainable Access to C-7 and C-15 Oxygenated Abietanes.

ChemSusChem·2026
Same author

Binding pose analysis and scaffold optimization of petasis products for selective COX-2 inhibition.

European journal of medicinal chemistry·2026
Same author

Preclinical validation of tetrahydroquinoline derivatives as EGFR inhibitor inducing glioblastoma cell death.

European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences·2026
Same journal

An intrinsically stretchable nanowire-based sensing patch for wearable analysis of sweat chloride ion composition.

Chemical communications (Cambridge, England)·2026
Same journal

A sterically rigid-flexible balanced NHC-Pd precatalyst for room-temperature solvent-free C-N coupling of benzocyclic amines.

Chemical communications (Cambridge, England)·2026
Same journal

Portable fluorescent conjugated microporous polymer sensor coupled with a smartphone for on-site Fe<sup>3+</sup> detection in water.

Chemical communications (Cambridge, England)·2026
Same journal

Accelerated discovery of NO<sub>3</sub>RR single-atom catalysts <i>via</i> high-throughput DFT and machine learning.

Chemical communications (Cambridge, England)·2026
Same journal

Wafer-scale robust graphene electronics under industrial processing conditions.

Chemical communications (Cambridge, England)·2026
Same journal

Subnanoscale IrW oxide anodes: breaking immiscibility for high activity and durability in water electrolysis.

Chemical communications (Cambridge, England)·2026
See all related articles

Researchers developed sustainable synthetic organic chemistry methods. These include catalyst reuse via dissolution in water and ionic liquids, and asymmetric transformations using chiral ionic liquids.

Area of Science:

  • Synthetic organic chemistry
  • Green chemistry

Background:

  • Traditional synthetic methods often generate significant waste.
  • Catalyst recovery and reuse remain challenges in organic synthesis.
  • Developing environmentally benign chemical processes is crucial.

Purpose of the Study:

  • To describe advancements in sustainable synthetic organic chemistry.
  • To highlight methods for catalyst reuse.
  • To showcase asymmetric transformations using chiral ionic liquids.

Main Methods:

  • Catalyst dissolution in water for reuse.
  • Catalyst dissolution in ionic liquids for reuse.
  • Asymmetric synthesis employing readily available chiral ionic liquids.

Main Results:

Related Experiment Videos

  • Demonstrated successful catalyst reuse through simple dissolution techniques.
  • Achieved efficient asymmetric transformations using accessible chiral ionic liquids.
  • Presented attractive and sustainable synthetic strategies.

Conclusions:

  • Simple dissolution in water and ionic liquids enables effective catalyst reuse.
  • Chiral ionic liquids offer a viable route for asymmetric synthesis.
  • These approaches contribute to greener synthetic organic chemistry.