17826-14-1Relevant academic research and scientific papers
Controlling the rates of reductively-activated elimination from the (indol-3-yl)methyl position of indolequinones
Everett, Steven A.,Naylor, Matthew A.,Barraja, Paola,Swann, Elizabeth,Patel, Kantilal B.,Stratford, Michael R. L.,Hudnott, Anna R.,Vojnovic, Borivoj,Locke, Rosalind J.,Wardman, Peter,Moody, Christopher J.
, p. 843 - 860 (2007/10/03)
A series of substituted 3-(4-nitrophenyloxy)methylindole-4,7-diones (Q) were synthesised. The effects of substitution patterns on the indole core on rates of elimination of 4-nitrophenol as a model for drug release following fragmentation of a phenolic et
