Concept

Phosphorus tribromide

Related publications (11)

Developing the Catalytic Applications of 1,3,2-Diazaphospholenes

The development of new catalytic methods for organic synthesis is a critical endeavour in order to obviate the economic and ecological drawbacks of stoichiometric organic synthesis. While catalysis can offer significant advantages in terms of atom-economy, ...

EPFL2021

Photocatalytic Decarboxylative Coupling of Aliphatic N-hydroxyphthalimide Esters with Polyfluoroaryl Nucleophiles

Xile Hu, Lara Lavrencic, Runze Mao, Xiangli Yi

Polyfluoroarenes are an important class of compounds in medical and material chemistry. The synthesis of alkylated polyfluoroarenes remains challenging. Here we describe a decarboxylative coupling reaction of N-hydroxyphthalimide esters of aliphatic carbox ...

WILEY-V C H VERLAG GMBH2021

Ruthenium on phosphorous-modified alumina as an effective and stable catalyst for catalytic transfer hydrogenation of furfural

Davide Ferri, Oliver Kröcher, Gaël Peng

Supported ruthenium was used in the liquid phase catalytic transfer hydrogenation of furfural. To improve the stability of Ru against leaching, phosphorous was introduced on a Ru/Al2O3 based catalyst upon impregnation with ammonium hypophosphite followed b ...

2020

Drivers of soil carbon stabilization in oil palm plantations

Alexandre Buttler, Thomas Guillaume, Mathieu Raymond Santonja, Juan Carlos Quezada Rivera, Johanna Katharina Rüegg

Increasing soil organic carbon (SOC) in agroecosystems is necessary to mitigate climate change and soil degradation. Management practices designed to reach this goal call for a deeper understanding of the processes and drivers of soil carbon input stabiliz ...

WILEY2019

MOF-Derived Cobalt Phosphide/Carbon Nanocubes for Selective Hydrogenation of Nitroarenes to Anilines

Wendy Lee Queen, Emad Oveisi, Daniel Teav Sun, Shuliang Yang, Li Peng, Mehrdad Asgari, Olga Trukhina, Safak Bulut

Transition-metal phosphides have received tremendous attention during the past few years because they are earth-abundant, cost-effective, and show outstanding catalytic performance in several electrochemically driven conversions including hydrogen evolutio ...

2018

Bromide Sources and Loads in Swiss Surface Waters and Their Relevance for Bromate Formation during Wastewater Ozonation

Urs von Gunten

Bromide measurements and mass balances in the catchments of major Swiss rivers revealed that chemical industry and municipal waste incinerators are the most important bromide sources and account for similar to 50% and similar to 20%, respectively, of the s ...

American Chemical Society2016

Patterned growth of high aspect ratio silicon wire arrays at moderate temperature

Vasiliki Tileli

High aspect ratio silicon wire arrays with excellent pattern fidelity over wafer-scale area were grown by chemical vapor deposition at moderate temperature, using a gas mixture of silane and hydrogen chloride. An innovative two-step process was developed f ...

2011

A Well-Defined Ni Pincer Catalyst for Cross Coupling of Non-Activated Alkyl Halides and Direct C-H Alkylation

Oleg Vechorkin

Carbon-carbon bond forming reactions are among the most important and useful methods for organic synthesis. During the last years, significant progress has been made in this field. Whereas many catalysts were developed for the coupling of aryl, alkenyl, an ...

EPFL2011

Functional group tolerant Kumada-Corriu-Tamao coupling of non-activated alkyl halides with aryl and heteroaryl nucleophiles: Catalysis by a nickel pincer complex permits the coupling of functionalized Grignard reagents

Xile Hu, Oleg Vechorkin, Valérie Proust

A nickel(II) pincer complex [(MeNN2)NiCl] (1) catalyzes Kumada−Corriu−Tamao cross coupling of nonactivated alkyl halides with aryl and heteroaryl Grignard reagents. The coupling of octyl bromide with phenylmagnesium chloride was used as a test reaction. Us ...

2009

Brominated 4-(trifluoromethyl)pyrimidines: A convenient access to versatile intermediates. [Erratum to document cited in CA141:395506]

Levente Ondi

Throughout the paper, the incorrect reagent names "phosphorus tribromide" and "phosphorus trichloride" should be replaced by the correct names "phosphoric tribromide" (POBr3) and "phosphoric trichloride" (POCL3). [on SciFinder (R)] ...

2004

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