107388-32-9Relevant academic research and scientific papers
Using the Wittig reaction to produce alkenylcarbaboranes
Sousa-Pedrares, Antonio,Vinas, Clara,Teixidor, Francesc
, p. 2998 - 3000 (2010)
This communication reports the first use of the Wittig reaction to produce alkenylcarbaboranes. The Royal Society of Chemistry 2010.
Reversible intramolecular photocycloaddition of a bis(9-anthrylbutadienyl) paracyclophane - An inverse photochromic system. (Photoactive cyclophanes 5)
Hopf, Henning,Beck, Christian,Desvergne, Jean-Pierre,Bouas-Laurent, Henri,Jones, Peter G.,Ernst, Ludger
, (2009)
The title compound, 4,13-bis[(1E,3E)-4-(9-anthracenyl)buta-1,3-dienyl][2.2] paracyclophane (2), prepared in 35% overall yield from [2.2]paracyclophane, absorbs light at λmax = 400 nm with a tail down to 480 nm. By irradiation into this band, 2
Syntheses of terminally substituted conjugated polyenes
Effenberger,Schlosser
, p. 1085 - 1094 (2007/10/02)
Polyenes and polyenals of the carotenoid type with five, nine and thirteen conjugated double bonds and a variety of terminally substituents like benzenes, naphthalenes, anthracenes, and tetraphenyl porphyrines are synthesized via Wittig reactions starting from crocetin dialdehyde or 2,7-dimethyloctatriendial, respectively. The characterization, and in most cases also the separation, of the E/Z-isomers of the polyenes is possible.
