Coumarinylmethyl caging groups with redshifted absorption

L Fournier, I Aujard, T Le Saux, S Maurin…

Index: Fournier, Ludovic; Aujard, Isabelle; Le Saux, Thomas; Maurin, Sylvie; Beaupierre, Sandra; Baudin, Jean-Bernard; Jullien, Ludovic Chemistry - A European Journal, 2013 , vol. 19, # 51 p. 17494 - 17507

Full Text: HTML

Citation Number: 18

Abstract

Abstract The small and synthetically easily accessible coumarinylmethyl backbone has been modified to generate a family of photolabile protecting groups with redshifted absorption. We relied on introducing electron-donating groups in the 7 position and electron-withdrawing groups in the 2-, and 2-and 3 positions. In particular, we showed that the diethylamino- thiocoumarylmethyl and the diethylamino-coumarylidenemalononitrilemethyl are relevant ...

Related Articles:

A convenient procedure for the synthesis of substituted 4-methylaminocoumarins

[Al-Zghoul, Khadeejh H.; Salih, Kifah S.M.; Ayoub, Mikdad T.; Mubarak, Mohammad S. Heterocycles, 2005 , vol. 65, # 12 p. 2937 - 2947]

More Articles...