130248-50-9

Upstream product

• 696-62-8 para-iodoanisole 
• 1066-54-2 trimethylsilylacetylene 
• 136618-41-2 E-2'-p-methoxystyryl iodide 

Downstream Products

• 38068-98-3 6-(4-methoxyphenyl)fulvene 
• 130248-51-0 {3-[1-(4-Methoxy-phenyl)-meth-(Z)-ylidene]-cyclopenta-1,4-dienyl}-trimethyl-silane 
• 130274-37-2 1-(4-methoxybenzyl)-2,4-bis(trimethylsilyl)cyclopentane 
• 57918-63-5 (Z)-styryl iodide 
• 130248-52-1 6-phenyl-3-(trimethylsilyl)fulvene 
• 130274-38-3 (E)-1,3-bis(trimethylsilyl)-6-phenylfulvene 

Relevant academic research and scientific papers

Palladium-Catalyzed Regio- and Stereoselective Synthesis of (E)-1,3-Bissilyl-6-arylfulvenes from Aryl Iodides and Silylacetylenes

An efficient synthetic route to (E)-1,3-bissilyl-6-arylfulvenes has been developed. The reaction of aryl iodides with trimethylsilylacetylene in the presence of a catalytic amount of PdBr2 gives 6-aryl-1,3-bis(trimethylsilyl)fulvenes in good to

Electrochemical Properties and Electrochromism of 6-Aryl-1,3-bis(trimethylsilyl)fulvenes and Their Derivatives

In this study, we have disclosed intriguing electrochromic properties of 6-aryl-1,3-bissilylfulvenes. The electrolyte solutions (0.1 M n-Bu4NClO4 in acetonitrile or dichloromethane) of some 6-aryl-1,3-bissilylfulvenes showed notable

A new synthesis of substituted fulvenes

A new fulvene synthesis results from the palladium-catalyzed [2 + 2 + 2] annulation of 1 mol of a β-substituted vinyl iodide and 2 mol of a monosubstituted acetylene. This variant of the Heck reaction tolerates a wide range of substrate substituents with