320718-03-4

Upstream product

• 96-13-9 2,3-Dibromopropan-1-ol 
• 88-05-1 2,4,6-trimethylaniline 

Downstream Products

• 923599-77-3 C₃₂H₅₀N₃O₅Si⁽¹⁺⁾*Cl^(1-) 
• 1415585-09-9 3-(tert-butyldimethylsilyloxy)-N¹,N²-dimesitylpropane-1,2-diamine 
• 1415585-10-2 5-[(tert-butyldimethylsilyloxy)methyl]-1,3-dimesityl-4,5-dihydro-1H-imidazol-3-ium chloride 
• 1616735-57-9 1-(oct-7-en-1-yloxy)-N,N'-dimesityl-2,3-diamino-1-propanol 
• 1616735-56-8 1-(hex-5-en-1-yloxy)-N,N'-dimesityl-2,3-diamino-1-propanol 
• 1262840-31-2 1-(allyloxy)-N,N'-dimesityl-2,3-diamino-1-propanol 
• 951787-52-3 C₅₀H₆₆N₄O₂ 
• 475585-40-1 N,N'-dimesityl-2,3-diamino-1-propoxytrimethylsilane 

Relevant academic research and scientific papers

An immobilised grubbs 2nd generation catalyst for application in flow-through devices

An improved immobilised Grubbs 2nd generation catalyst and its application in flow-through devices, shown for on-column reaction gas chromatography (ocRGC), has been studied. The coupling of a reaction capillary and a separation column in GC/MS

Alkynyl-functionalized imidazolium for "click" dendrimer functionalisation and palladium nanoparticle stabilization

Functionalization of imidazolium salts (IMSs) that allow easy derivation of molecular or solid supports are called for in various applications. Here, the synthesis of an alkyne-containing IMS can be achieved in three steps from 2,4,6-trimethylaniline, and

Ruthenium Complex Bearing a Hydroxy Group Functionalised N-Heterocyclic Carbene Ligand – A Universal Platform for Synthesis of Tagged and Immobilised Catalysts for Olefin Metathesis

Six olefin metathesis catalysts, based on a common ruthenium precursor featuring a hydroxy-substituted N-heterocyclic carbene ligand, were successfully prepared and fully characterised. As proof-of-concept, two of them ([Ru]isonico and [Ru]sub

Ruthenium olefin metathesis catalysts featuring n-heterocyclic carbene ligands tagged with isonicotinic and 4-(Dimethylamino)benzoic acid rests: Evaluation of a modular synthetic strategy

A modular and flexible strategy towards the synthesis of N-heterocyclic carbene (NHC) ligands bearing Br?nsted base tags has been proposed and then adopted in the preparation of two tagged NHC ligands bearing rests of isonicotinic and 4-(dimethylamino)benzoic acids. Such tagged NHC ligands represent an attractive starting point for the synthesis of olefin metathesis ruthenium catalysts tagged in non-dissociating ligands. The influence of the Br?nsted basic tags on the activity of such obtained olefin metathesis catalysts has been studied.

Self-supported oligomeric grubbs/hoveyda-type Ru - Carbene complexes for ring-closing metathesis

On the basis of the release-return metathesis mechanism, self-supported oligomeric Grubbs/Hoveyda-type Ru-carbene complexes have been designed and synthesized as a new type of recoverable catalyst for ring-closing metathesis. The catalytic activities of t

Synthesis of a silica-based heterogeneous second generation grubbs catalyst

The synthesis of a second generation Grubbs catalyst immobilized onto non-porous silica is described. For this purpose, a polymerizable cationic NHC precursor, 1,3-bis(1-mesityl)-4-{[(bicyclo[2.2.1]hept-5-en-2-ylcarbonyl)oxy] methyl}-4,5-dihydro-1H-imidaz