55020-66-1

Upstream product

• 100-39-0 benzyl bromide 
• 87-66-1 2-hydroxyresorcinol 

Downstream Products

• 1262725-18-7 C₄₂H₅₂O₁₂ 
• 1262725-16-5 C₂₉H₄₄O₁₁ 
• 1256601-70-3 C₃₈H₄₄O₁₀ 
• 1256601-66-7 C₂₅H₃₆O₉ 
• 147825-65-8 2,6-bis(1-methylethoxy)phenol 
• 867258-38-6 22-benzyloxy-2,8,11,17-tetraoxa-5,14-diazabicyclo[16.3.1]docosa-1⁽²¹⁾,18⁽²²⁾,19-triene-4,15-dione 
• 765915-42-2 (2-benzyloxy-3-methoxycarbonylmethoxy-phenoxy)-acetic acid methyl ester 
• 765915-41-1 2-benzyloxy-4-bromo-benzene-1,3-diol 
• 147825-64-7 1,3-bis(1-methylethoxy)-2-(phenylmethoxy)benzene 
• 765915-43-3 (2-benzyloxy-6-bromo-3-methoxycarbonylmethoxy-phenoxy)-acetic acid methyl ester 

Relevant academic research and scientific papers

Total Synthesis of Actinorhodin

The enantioselective total synthesis of actinorhodin (1) is described. The synthesis features 1) dual benzyne reactions en route to the monomer, 2) the trans-selective installation of the side chain, and 3) a regioselective oxidative dimerization.

Improved and controlled complexation of paraquat derivatives by the formation of a bis(m-phenylene)-26-crown-8-based lariat ether

A novel bis(m-phenylene)-26-crown-8-based lariat ether (i.e., 3b) was synthesized and characterized. It can bind paraquat derivatives more strongly than bis(m-phenylene)-26-crown-8 in solution. It forms pseudorotaxanes with two paraquat derivatives in the

A versatile approach to the synthesis of pendant benzodiazacoronands

A versatile approach to the synthesis of pendant benzodiazacoronands is presented. Macrocyclic compounds possessing intra-annular amine or hydroxy group were obtained and N-benzamide, O-benzyl or O-benzoyl side-arms were introduced into such a macrocyclic

Efficient synthesis of new macrocycles with planar chirality

Two new macrocycles possessing planar chirality were efficiently synthesized and resolved into enantiomers employing HPLC. CD spectra of 11 and 12 confirm their enantiomeric relationship and chiral stability.

Benzylamine Antioxidants: Relationship between Structure, Peroxyl Radical Scavenging, Lipid Peroxidation Inhibition, and Cytoprotection

Three homologous series of 3,5-dialkoxy-4-hydroxybenzylamines were prepared and tested (1) as peroxyl radical scavengers in homogeneous aqueous solution, (2) as inhibitors of iron-dependent peroxidation of rabbit brain vesicular membrane lipids, and (3) a