262268-62-2Relevant academic research and scientific papers
An efficient method for one-carbon elongation of aryl aldehydes via their dibromoalkene derivatives
Huh, Dal Ho,Jeong, Ji Sang,Lee, Hee Bong,Ryu, Hoejin,Kim, Young Gyu
, p. 9925 - 9932 (2007/10/03)
Various aryl aldehydes were efficiently converted into one-carbon extended aryl acetamides or aryl acetic acids through the reaction of their dibromoalkene derivatives with pyrrolidine in the presence of water under very mild conditions.
A novel synthesis of β,β-dibromostyrenes
Shastin,Korotchenko,Nenajdenko,Balenkova
, p. 2081 - 2084 (2007/10/03)
A new simple and efficient transformation of aromatic aldehydes to β,β-dibromostyrenes and arylbromoacetylenes is described. The olefination procedure was conducted under mild conditions and in good yields.
Phenyl β-methoxyacrylates: A new antimalarial pharmacophore
Alzeer, Jawad,Chollet, Jacques,Heinze-Krauss, Ingrid,Hubschwerlen, Christian,Matile, Hugues,Ridley, Robert G.
, p. 560 - 568 (2007/10/03)
Phenyl β-methoxyacrylates, linked to an aromatic ring via an olefinic bridge, have been identified as novel, potentially inexpensive, antimalarial agents. The compounds are believed to exert their activity by inhibition of mitochondrial electron transport
Synthesis and Non-Linear Optical Properties of Diacetylenes with Conjugated Side Groups
Wright, J.,Milburn, G. H. W.,Shand, A. J.,Werninck, A. R.,Coles, H. J.,Smith, D. A. McL
, p. 1 - 14 (2007/10/02)
Seven novel diacetylenes have been synthesised, with six of these containing a pyridine ring directly conjugated to the main diacetylene unit.Values of χ2 and χ3 for these diacetylenes as guests in a guest-host polymer matrix (polysi
