356568-04-2Relevant academic research and scientific papers
Visible-Light Induced Direct Synthesis of Polysubstituted Furans from Cyclopropyl Ketones
Feng, Liyan,Yan, Hang,Yang, Chao,Chen, Dafa,Xia, Wujiong
, p. 7008 - 7022 (2016/08/30)
In this article, a photoredox protocol for the synthesis of furans via oxidative coupling of olefin generated in situ from cyclopropyl ketones with ketonic oxygen atom is presented. Moreover, bromination of furans in the presence of overstoichiometric oxidant has been achieved with high regioselectivity.
Access to 2,5-diamidopyrroles and 2,5-diamidofurans by Au(I)-catalyzed double hydroamination or hydration of 1,3-diynes
Kramer, Soren,Madsen, Julie L. H.,Rottlaender, Mario,Skrydstrup, Troels
supporting information; experimental part, p. 2758 - 2761 (2010/08/22)
(Figure presented) A Au(I)-catalyzed hydroamination or hydration of 1,3-diynes to access 2,5-diamidopyrroles and 2,5-diamidofurans has been developed. This method can also be expanded to 2,5-disubstituted furans and 1,2,5-trisubstituted pyrroles including the formation of deuterated heterocycles and 18O-labeled furans.
Distribution of furamidine analogues in tumor cells: Influence of the number of positive charges
Lansiaux, Amélie,Dassonneville, Laurent,Facompré, Micha?l,Kumar, Arvind,Stephens, Chad E.,Bajic, Miroslav,Tanious, Farial,Wilson, David W.,Boykin, David W.,Bailly, Christian
, p. 1994 - 2002 (2007/10/03)
Fluorescence microscopy has been used to study the cellular distribution properties of a series of DNA binding cationic compounds related to the potent antiparasitic drug furamidine (DB75). The compounds tested bear a diphenylfuran or a phenylfuranbenzimi
