Chemical Reactions
Chemical Reactions

Synthetic Strategy – Lecture 2 (DC, 19.1.05)
Synthetic Strategy – Lecture 2 (DC, 19.1.05)

Handbook for the Lab Course Organic Chemistry I
Handbook for the Lab Course Organic Chemistry I

Chemomimetic Biocatalysis: Exploiting the Synthetic Potential of
Chemomimetic Biocatalysis: Exploiting the Synthetic Potential of

First palladium- and nickel-catalyzed oxidative
First palladium- and nickel-catalyzed oxidative

... amination of aryl and alkenyl groups [22], which usually requires higher reaction temperatures, especially for electron-demanding nitrogen groups. In addition, the present protocols for diamination do not require ligand fine-tuning, but rather proceed under ligand-free conditions. In summary, we hav ...
Product Selectivity in Homogeneous Artificial Photosynthesis Using
Product Selectivity in Homogeneous Artificial Photosynthesis Using

Faculteit der Natuurwetenschappen, Wiskunde en Informatica
Faculteit der Natuurwetenschappen, Wiskunde en Informatica

Influence of alkyl chain length on sulfated zirconia catalysed batch
Influence of alkyl chain length on sulfated zirconia catalysed batch

Porous Organic Polymers in Catalysis: Opportunities and Challenges
Porous Organic Polymers in Catalysis: Opportunities and Challenges

applied sciences Chiral β-Amino Alcohols as Ligands for the N
applied sciences Chiral β-Amino Alcohols as Ligands for the N

Hydrogenation, Transfer Hydrogenat- ion and Hydrogen Transfer Reactions
Hydrogenation, Transfer Hydrogenat- ion and Hydrogen Transfer Reactions

Abdullah F. Eid
Abdullah F. Eid

Synthesis of (−)-Epibatidine - David A. Evans
Synthesis of (−)-Epibatidine - David A. Evans

Formic acid oxidation reaction on a PdxNiy bimetallic nanoparticle
Formic acid oxidation reaction on a PdxNiy bimetallic nanoparticle

Nonracemic Allylic Boronates through Enantiotopic-Group
Nonracemic Allylic Boronates through Enantiotopic-Group

Study on the Reduction of Molybdenum Dioxide by Hydrogen
Study on the Reduction of Molybdenum Dioxide by Hydrogen

Methane storage in mixed hydrates with tetrahydrofuran
Methane storage in mixed hydrates with tetrahydrofuran

Chapter 1 Organoaluminum Reagents for Selective Organic
Chapter 1 Organoaluminum Reagents for Selective Organic

Development of Lewis Acid Mediated Stereoselective Synthesis of
Development of Lewis Acid Mediated Stereoselective Synthesis of

Organometallic Compounds - Reagents
Organometallic Compounds - Reagents

... synthesis by reasoning backward from the the target molecule to a starting compound using known and reliable reactions. “it is a problem solving technique for transforming the structure of a synthetic target molecule (TM) to a sequence of progressively simpler structures along the pathway which ulti ...
NUCLEOPHILIC SUBSTITUTION & ELIMINATION ON Csp 3
NUCLEOPHILIC SUBSTITUTION & ELIMINATION ON Csp 3

ON THE ROAD TO CARBENE AND CARBYNE COMPLEXES
ON THE ROAD TO CARBENE AND CARBYNE COMPLEXES

Grignard Reagents
Grignard Reagents

4 ORGANIC CHEMISTRY: STRUCTURE AND NOMENCLATURE
4 ORGANIC CHEMISTRY: STRUCTURE AND NOMENCLATURE

Relevance of the Physicochemical Properties of Calcined Quail
Relevance of the Physicochemical Properties of Calcined Quail

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.