65684-00-6

Upstream product

• 27410-09-9 3-(p-Anisyl)-1,4-pentadiin-3-ol 
• 77-78-1 dimethyl sulfate 
• 801287-26-3 1-trimethylsilyl-3-(4-methoxyphenyl)penta-1,4-diyn-3-ol 
• 99048-48-3 1‐(4‐methoxyphenyl)‐3‐(trimethylsilyl)prop‐2‐yn‐1‐one 
• 100-07-2 4-methoxy-benzoyl chloride 

Downstream Products

• 65683-92-3 4-(p-Anisyl)-1,4-dihydro-4-methoxy-1-phenylarsenin 
• 65683-92-3 4-(p-Anisyl)-1,4-dihydro-r-4-methoxy-c-1-phenylarsenin 
• 65683-92-3 4-(p-Anisyl)-1,4-dihydro-r-4-methoxy-t-1-phenylarsenin 
• 80239-03-8 4-(p-Anisyl)-1,4-dihydro-r-4-methoxy-c-1-(p-tolyl)arsenin 
• 80239-03-8 4-(p-Anisyl)-1,4-dihydro-r-4-methoxy-t-1-(p-tolyl)arsenin 

Relevant academic research and scientific papers

Synthesis and stereochemical resolution of functional [5]pericyclynes

Three different kinds of ring carbo-mers of [5]cyclitol ethers were targeted as challenging examples of functional [5]pericyclynes. Three tertiary pentaaryl-carbo-[5]cyclitol methyl ethers were synthesized through a [11+4] ring-closing double addition of

Synthesis of 2-Aryl-(2-R)-arsenines by Cyclohexadienol -> Arsabenzene Rearrangement

KOH/crown-6 phase-transfer catalyzed addition of arylarsines (phenylarsine, p-tolylarsine) to the (3-R)-3-methoxy-1,4-pentadiynes 13 yields the cis/trans isomeric 1-aryl-1,4-dihydro-(4-R)-4-methoxyarsenines, the 1H-NMR- and 13C-NMR spectra of which ar