163301-93-7

Upstream product

• 108-88-3 toluene 
• 71400-25-4 1,3-phenylenebis[(4-methylphenyl)methanone] 
• 99-63-8 benzene-1,3-dicarbonyl dichloride 

Downstream Products

• 1414888-81-5 C₃₇H₂₉N₂O₂⁽¹⁺⁾*Cl^(1-) 
• 1414888-87-1 C₃₆H₃₀N₂O₂ 
• 163301-94-8 1,3-bis[4-[(1-benzyloxyureido)methyl]benzoyl]benzene 
• 597576-22-2 [3-(4-mercaptomethyl-benzoyl)-phenyl]-(4-mercaptomethyl-phenyl)-methanone 

Relevant academic research and scientific papers

Design and synthesis of novel chiral dihydroimidazolium cyclophanes as N-heterocyclic carbene precatalysts

A series of novel diphenyl ethylenediamine (DPEN) derived C2 symmetric dihydroimidazolium cyclophanes were designed and synthesized as organo NHC precatalysts. The resultant organo NHC-catalyzed reactions with superior enantioselectivity than t

Design and synthesis of novel chiral dihydroimidazolium cyclophanes as N-heterocyclic carbene precatalysts

A series of novel diphenyl ethylenediamine (DPEN) derived C2 symmetric dihydroimidazolium cyclophanes were designed and synthesized as organo NHC precatalysts. The resultant organo NHC-catalyzed reactions with superior enantioselectivity than t

Synthesis of annularly functionalized cyclophanes

Friedel-Crafts reaction of m- and p-benzenedicarboxylic acid chlorides with toluene gave diketones. The dicarbonyl dibromides, obtained by NBS bromination of diketones were coupled with various dithiols and dihydroxy benzenes to give cyclophanes incorpora

Synthesis of chiral cyclophanes based on meta-terphenyl and pyridyl blocks

Coupling of m-terphenyl dibromide with binol afforded the corresponding optically active cyclophane. Chiral cyclophanes were also obtained by the coupling of p-nitrophenol or 4,4″-bis(bromomethyl)-1,3-dibenzylbenzene with binol.

Bisoxadiazolidine derivative

A bisoxadiazolidine dione derivative represented by the following general formula (I) or a pharmaceutically acceptable salt thereof, which is useful as an insulin sensitivity-increasing drug, and a pharmaceutical composition thereof. STR1 each represents a phenylene group L: (1) an oxygen, (2) a STR2 (3) a --S(O)n --, (4) a --CO--, (5) a STR3 (6) an alkylene group or an alkenylene group which may respectively be interrupted with an oxygen atom and/or a sulfur atom.