61483-02-1

Upstream product

• 71616-84-7 4-methoxycarbonyl-4'-methoxybenzophenone 
• 1679-64-7 Monomethyl terephthalate 
• 100-66-3 methoxybenzene 
• 874-60-2 4-methyl-benzoyl chloride 
• 23886-71-7 4-methoxy-4'-methylbenzophenone 
• 201230-82-2 carbon monoxide 
• 696-62-8 para-iodoanisole 
• 14047-29-1 4-carboxyphenylboronic acid 

Downstream Products

• 1277177-55-5 C₃₃H₄₅N₂O₁₃P 

Relevant academic research and scientific papers

Novel and efficient bridged bis(N-heterocyclic carbene)palladium(II) catalysts for selective carbonylative Suzuki–Miyaura coupling reactions to biaryl ketones and biaryl diketones

Bridged N,N′-substituted bisbenzimidazolium bromide salts (L1, L2, and L3) were synthesized and fully characterized. Reactions of palladium acetate with L1, L2, and L3 afforded corresponding new bridged bis(N-heterocyclic carbene)palladium(II) complexes (C1, C2, and C3) in high yields. The X-ray structure of complex C1 showed that the Pd(II) ion is bonded to the two carbon atoms of the bis(N-heterocyclic carbene) and two bromido ligands are in the cis position, resulting in a distorted square planar geometry. The three Pd(NHC)2Br2 complexes C1, C2, and C3 were evaluated in carbonylative Suzuki–Miyaura coupling reactions of aryl boronic acids with aryl halides and displayed high catalytic activity with low catalyst loading. The coupling reactions of aryl bromides were selective towards the carbonylation product at higher carbon monoxide pressure.

PHOTOACTIVATABLE FOULING-RESISTANT COPOLYMERS

A photoactivatable fouling-resistant copolymer composed of a photoactivatable monomer and a hydrophilic monomer is disclosed. The photoactivatable monomer includes an aryl ketone derivative having one or more polar groups or alkyl groups.

Synthesis of trifunctional phosphatidylserine probes for identification of lipid-binding proteins

Phosphatidylserine (PS) lipids play a number of roles in cell biology, one of which is to mark apoptotic cells for clearance by macrophages. PS recognition triggers macrophage recognition and clearance, which occurs concomitantly with active suppression o

BENZAMIDINE DERIVATIVES

Benzamidine derivatives of the following formulae or analogs thereof, i. e., pharmaceutically acceptable salts thereof, are provided. These compounds or salts thereof have a blood-coagulation inhibiting effect based on an excellent effect of inhibiting the action of activated blood coagulation factor X, and they are useful as anticoagulants.