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solvents_family_EN_final AVL.indd
solvents_family_EN_final AVL.indd

Catalytic oxidation of ammonia to nitrogen
Catalytic oxidation of ammonia to nitrogen

B11MS1-Week10
B11MS1-Week10

Efficient Nickel-Catalyzed [2 + 2 + 2] Cycloaddition of CO2 and Diynes
Efficient Nickel-Catalyzed [2 + 2 + 2] Cycloaddition of CO2 and Diynes

Enolate Chemistry - Institut für Organische Chemie
Enolate Chemistry - Institut für Organische Chemie

2 Electrocatalytic Oxygen Reduction Reaction
2 Electrocatalytic Oxygen Reduction Reaction

A two-step approach for the catalytic conversion of glucose to 2,5
A two-step approach for the catalytic conversion of glucose to 2,5

Rhenium- and molybdenum-catalyzed dehydration reactions
Rhenium- and molybdenum-catalyzed dehydration reactions

13_lecture_ppt
13_lecture_ppt

... of Cu(OH)2 and sodium citrate – Reacts with aldehydes, but not with ketones – Cu2+ is reduced to Cu+ • Solution of Cu2+ is a distinctive blue color • Color fades during the reaction as Cu+ precipitates as the red solid, copper(I) oxide, Cu2O ...
Get cached PDF
Get cached PDF

Full-Text PDF
Full-Text PDF

... still there are chances to improve the catalysis in olefin metathesis [35,36], mainly due to the undesired parallel reactions [37–39], or low capability to deal with water or alcohols as solvents [40,41]. Even though molybdenum [42,43] and basically ruthenium are the metals reference in olefin metat ...
Lecture 1: Key Concepts in Stereoselective Synthesis
Lecture 1: Key Concepts in Stereoselective Synthesis

... -Da reported a similar indirect way of doing catalytic enantioselective Grignard addition. -Catalytic asymmetric addition was achieved by deactivating Grignard reagents through chelation with bis[2(N,N-dimethylamino)ethyl]ether (BDMAEE). -In this carbonyl addition reaction, MgBr2 and MgBr(OiPr) are ...
Living ring-opening metathesis polymerization
Living ring-opening metathesis polymerization

... associated with the release of ring-strain. These considerations are important when attempting the ROMP of any new cyclic olefin. Generally, the most favorable conditions for a successful ROMP reaction is to use the highest monomer concentration at the lowest temperature possible. ...
Process for preparing polycarbonates
Process for preparing polycarbonates

Asymmetric Synthesis: Substrate and Auxiliary Control
Asymmetric Synthesis: Substrate and Auxiliary Control

Nickel(II) Catalysts for Ethylene Homo
Nickel(II) Catalysts for Ethylene Homo

A comparative study of catalytic properties of ZnO and FeZnO
A comparative study of catalytic properties of ZnO and FeZnO

Ruthenium-Catalyzed Hydrogen Transfer Reactions
Ruthenium-Catalyzed Hydrogen Transfer Reactions

Postprint
Postprint

Learning materials
Learning materials

RheniumCatalyzed Deoxydehydration of Diols and Polyols
RheniumCatalyzed Deoxydehydration of Diols and Polyols

ligand design - UZH - Department of Chemistry
ligand design - UZH - Department of Chemistry

University of Groningen Reactivity of rare earth metal
University of Groningen Reactivity of rare earth metal

1.4. Nomenclature 2. LABORATORY
1.4. Nomenclature 2. LABORATORY

8 reactions of a cetylenes
8 reactions of a cetylenes

< 1 ... 3 4 5 6 7 8 9 10 11 ... 47 >

Fischer–Tropsch process

The Fischer–Tropsch process is a collection of chemical reactions that converts a mixture of carbon monoxide and hydrogen into liquid hydrocarbons. It was first developed by Franz Fischer and Hans Tropsch at the Kaiser-Wilhelm-Institut für Kohlenforschung in Mülheim an der Ruhr, Germany, in 1925. The process, a key component of gas to liquids technology, produces a synthetic lubrication oil and synthetic fuel, typically from coal, natural gas, or biomass. The Fischer–Tropsch process has received intermittent attention as a source of low-sulfur diesel fuel and to address the supply or cost of petroleum-derived hydrocarbons. A Fischer–Tropsch-type process has also been suggested to have produced a few of the building blocks of DNA and RNA within asteroids.
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