390367-06-3

Upstream product

• 565462-34-2 {4-[3-(4-hydroxymethyl-phenoxymethyl)-benzyloxy]-phenyl}-methanol 
• 626-15-3 1,3-bis-(bromomethyl)benzene 
• 123-08-0 4-hydroxy-benzaldehyde 
• 64879-82-9 C₂₄H₂₂O₆ 
• 99-76-3 methyl 4-hydroxylbenzoate 
• 163301-09-5 4,4′-[1,3-phenylenebis(methyleneoxy)]bisbenzaldehyde 

Downstream Products

• 1414888-83-7 C₃₇H₃₂N₂O₂S 
• 1414888-91-7 C₃₆H₃₄N₂O₂ 
• 683248-56-8 C₃₆H₃₀O₆ 
• 565462-35-3 {4-[3-(4-mercaptomethyl-phenoxymethyl)-benzyloxy]-phenyl}-methanethiol 

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

Dioxastilbenophanes - Synthesis and charge transfer complexation studies

Intramolecular McMurry coupling of dialdehydes derived from xylenyl dibromide and 4-hydroxy benzaldehyde afforded cis-stilbenophanes along with cyclophane diols. Stilbenophanes with a large cavity were also synthesized. Charge transfer complexations of th

Synthesis of an annularly linked bicyclic chiral cyclophane by pre-organization of a dibromide

An annularly linked bicyclic chiral cyclophane was synthesized from a suitable pre-organized chiral dibromide.

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.

Nitroethylenophanes - New class of novel cyclophanes

Reaction of o-xylenyl dibromide with dipotassium salt of 2-nitro-1,1-ethanedithiol afforded nitroethylenophane 2. Similar strategy has been used for the synthesis of cyclophanes 7, 9 and 11.