123711-71-7Relevant academic research and scientific papers
Synthesis, properties, and redox behavior of 1,1,4,4-tetracyano-2-ferrocenyl-1,3-butadienes connected by aryl, biaryl, and teraryl spacers
Shoji, Taku,Yaku, Chisa,Kamata, Natsumi,Maruyama, Akifumi,Ito, Shunji,Okujima, Tetsuo,Toyota, Kozo
, p. 402 - 409 (2015)
Aryl-substituted 1,1,4,4-tetracyano-1,3-butadienes (FcTCBDs) and bis(1,1,4,4-tetracyanobutadiene)s (bis- FcTCBDs), possessing a ferrocenyl group on each terminal, were prepared by the reaction of a variety of alkynes with tetracyanoethylene (TCNE) in a [2
Labeling of organic biomolecules with ethynylferrocene
Coutouli-Argyropoulou, Evdoxiq,Tsitabani, Maria,Petrantonakis, Georgios,Terzis, Aris,Raptopoulou, Catherine
, p. 1382 - 1388 (2003)
The Sonogashira coupling reaction of ethynylferrocene with adenine, uracil, tyrosine and steroid derivatives was studied; with the exception of tyrosine it was proved to be a good route for the attachment of ferrocene to these representative biomolecules. In addition the transformation of alkynyl uracil to furanopyrimidone derivative was investigated and the formation of the furanopyrimidone ring was confirmed by an X-ray crystallographic analysis carried out on product 16.
Metallation of alkynes: Part 10. Acetoxymercuration of arylferrocenylethynes
Carollo, Lorenzo,Floris, Barbara
, p. 80 - 85 (2007/10/03)
Arylferrocenylhethynes compounds reacted with mercuric acetate in acetic acid yielding mercurated addition compounds, the regiochemistry of which were determined by the strongly electron-donating ferrocenyl ring. Substituent effects on the reactivity are
