Concept

Reagent

Publications associées (57)

Copper-Catalyzed Oxy-Alkynylation of Diazo Compounds with Hypervalent Iodine Reagents

Alkynes have found widespread applications in synthetic chemistry, biology, and materials sciences. In recent years, methods based on electrophilic alkynylation with hypervalent iodine reagents have made acetylene synthesis more flexible and efficient, but ...

American Chemical Society2016

Cyclic Hypervalent Iodine Reagents for Atom-Transfer Reactions: Beyond Trifluoromethylation

Jérôme Waser, Durga Prasada Rao Hari, Yifan Li, Maria Victoria Vita

Hypervalent iodine compounds are privileged reagents in organic synthesis because of their exceptional reactivity. Among these compounds, cyclic derivatives stand apart because of their enhanced stability. They have been widely used as oxidants, but their ...

Wiley-Blackwell2016

Accelerated methylene blue (MB) degradation by Fenton reagent exposed to UV or VUV/UV light in an innovative micro photo-reactor

César Pulgarin, Juan Kiwi, Mengkai Li

This study presents the accelerated discoloration/degradation of methylene blue (MB) in solution by Fenton reagent under exposure to ultraviolet (UV) or Vacuum-UV/UV (VUV/UV) light in an innovative micro photo-reactor. The MB degradation was kinetically fa ...

Elsevier2016

Alkynylation with Hypervalent Iodine Reagents

Jérôme Waser

Alkynes are among the most versatile functional groups in organic synthesis. They are also frequently used in chemical biology and materials science. Whereas alkynes are traditionally added as nucleophiles into organic molecules, hypervalent iodine reagent ...

Springer Verlag2015

Phase-resolved particle size distribution: New insight into material characterization

Christian Ludwig, Andrea Testino

Particle size distribution (PSD) is a relevant property of powdered solid matter since it directly influences the functionality of solid products such as pharmaceutics, cosmetics, abrasives, ceramics, metals, pigments, catalysts, and chemical reactants. Se ...

Elsevier2015

Reactions of Grignard Reagents with Nitrous Oxide

Rosario Scopelliti, Kay Severin, Euro Solari, Alexander Tskhovrebov

The chemical activation of nitrous oxide (N2O) can be achieved by organocalcium, organosodium, and organolithium compounds. Grignard reagents, on the other hand, are believed to be inert. We demonstrate that this generalization is not correct. Some aliphat ...

American Chemical Society2014

Structural cluster analysis of chemical reactions in solution

Fabio Pietrucci

We introduce a simple and general approach to the problem of clustering structures from atomic trajectories of chemical reactions in solution. By considering distance metrics which are invariant under permutation of identical atoms or molecules, we demonst ...

Amer Inst Physics2013

Inactivation by solar photo-Fenton in pet bottles of wild enteric bacteria of natural well water: Absence of re-growth after one week of subsequent storage

César Pulgarin, Juliette Ndounla

Iron photo-assisted inactivation of wild enteric bacteria (total coliforms/E. coil and Salmonella spp.) was carried out in water from the Sahelian wells having different pH (W1:4.9 and W2: 6.3) and a natural iron content of 0.07 mg/L We evaluate the effici ...

Elsevier2013

Protein tag-mediated conjugation of oligonucleotides to recombinant affinity binders for proximity ligation

Kai Johnsson

While antibodies currently play a dominant role as affinity reagents in biological research and for diagnostics, a broad range of recombinant proteins are emerging as promising alternative affinity reagents in detection assays and quantification. DNA-media ...

Elsevier2013

Oxidative Coupling Reactions of Grignard Reagents with Nitrous Oxide

Kay Severin, Gregor Kiefer, Loïc Nicolas Jeanbourquin

Catalysis with laughing gas: N2O in combination with transition-metal catalysts allow the oxidative homo- and cross-coupling of Grignard reagents. The reactions can be performed under mild conditions despite the inert character of N2O. ...

Wiley-Blackwell2013

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