Results 231 to 240 of about 73,410 (278)
Enhancing the Chemical Reactivity of Graphene through Substrate Engineering
This review highlights methods to enhance the reactivity of graphene through substrate engineering, focusing on strain and charge doping. Strains induced by nanoparticles, metal crystal orientations, or stretchable polymers increase the reactivity of graphene.
Jia Tu, Mingdi Yan
wiley +1 more source
Versuche zur asymmetrischen Redox-Disproportionierung von meso-Peroxiden. Neue Chrom(III)-und Organokatalysatoren für die asymmetrische Hetero-Diels-Alder Reaktion [PDF]
Vogl, Nadine
core
Self‐nanostructuring of redox‐active organic small molecules through in situ electrochemical postcrosslinking enabled an aqueous‐processed, stable, fast‐rechargeable organic electrode even with a high active content ratio and mass loading. ABSTRACT Redox‐active organic materials (ROMs) for batteries are emerging as sustainable alternatives to inorganic
Kyunam Lee +16 more
wiley +1 more source
A scalable triazine‐based covalent functionalization strategy of black phosphorus nanosheets provides controlled P‐N surface chemistry with enhanced grafting density in the presence of a phase‐transfer catalyst. As a representative example, BP‐sulfated polymer conjugates exhibit strong in vitro antiviral activity against enveloped viruses and ...
Jasmin Er +18 more
wiley +1 more source
Advances in the Different Synthetic Routes of Fluorinated Hydrazines
This review highlights the various routes to the preparation of fluorinated hydrazines, thereby promoting the exploration of innovative methods for the synthesis of new N‐fluorinated hydrazines. Their synthesis mainly involves synthetic routes such as organometallic, organocatalytic, and photocatalytic.
Dimitra Kyrko, Benoît Crousse
wiley +1 more source
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2010
This chapter deals with enantioselective organocatalytic cycloaddition reactions. Several cinchona alkaloids have been recently demonstrated as efficient chiral organocatalysts for enantioselective Diels−Alder reactions. Thus, excellent results were obtained for the Diels−Alder reaction of 3-vinylindoles with maleimides catalysed by a ...
S. Araki, T. Hirashita
+4 more sources
This chapter deals with enantioselective organocatalytic cycloaddition reactions. Several cinchona alkaloids have been recently demonstrated as efficient chiral organocatalysts for enantioselective Diels−Alder reactions. Thus, excellent results were obtained for the Diels−Alder reaction of 3-vinylindoles with maleimides catalysed by a ...
S. Araki, T. Hirashita
+4 more sources
Microwave-assisted cycloaddition reactions
Chem. Soc. Rev., 2010Cycloaddition reactions belong to one of the most well-investigated and widely used reactions in synthetic organic chemistry for the construction of (hetero)cyclic compounds in a single-step operation. In this tutorial review, a select number of examples of some [3+2] cycloadditions, i.e. for 1,2,3-triazole formation, as well as of some [4+2] and [2+2]
Prasad, Appukkuttan +2 more
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Retro‐Cycloaddition Reaction of Pyrrolidinofullerenes.
ChemInform, 2005AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Nazario, Martín +5 more
openaire +2 more sources

