26582-44-5Relevant articles and documents
A simple and effective approach to the synthesis of pyrido[4,3,2-mn]pyrrolo[3,2,1-de]acridine skeleton of arnoamines A and B, pentacyclic marine alkaloids from the ascidian Cystodytes sp.
Radchenko, Oleg S.,Balaneva, Nadezhda N.,Denisenko, Vladimir A.,Novikov, Vyacheslav L.
, p. 7819 - 7822 (2007/10/03)
Starting from ethyl 5-hydroxy-2-methyl-1-phenylindole-3-carboxylate, a simple and effective approach to the synthesis of pyrido[4,3,2-mn]pyrrolo[3,2,1-de]acridine skeleton of arnoamines A and B, unique pentacyclic alkaloids from the ascidian Cystodytes sp
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