712352-30-2Relevant academic research and scientific papers
Towards configurationally stable bisindolylmaleimide cyclophanes: potential tools for investigating protein kinase function.
Bartlett, Stephen,Nelson, Adam
, p. 1112 - 1113 (2004)
The effect of macrocycle size and substitution on the configurational stability of some bisindolylmaleimide cyclophanes was determined.
Evaluation of alternative approaches for the synthesis of macrocyclic bisindolylmaleimides
Bartlett, Stephen,Nelson, Adam
, p. 2874 - 2883 (2007/10/03)
Approaches for the synthesis of macrocyclic bisindolylmaleimides, in which the indole nitrogens are linked with a tether, are described. Two alternative approaches were investigated: macrocyclisation in either the southern (by adding the tether to the bisindolylmaleimide ring system) or the northern district. With two-, three-and four-atom tethers, both of these approaches were unsuccessful for a wide range of attempted macrocyclisation reactions (palladium-catalysed π-allyl substitution, ring-closing metathesis, McMurry reaction, iodocyclisation, formation of a silylene derivative, substitution of an α,ω-disubstituted electrophile). The failure of all of these reactions was ascribed to the strained nature of the target ring system. However, with longer tethers (six to ten atoms), the macrocycles could prepared using either a ring-closing metathesis reaction or by substitution of an α,ω-dibromide). Fourteen successful macrocyclisation reactions are described; deprotection gave eleven macrocyclic bisindolylmaleimides in which an imide substituent had been removed.
