138498-84-7Relevant academic research and scientific papers
Dynamic combinatorial chemistry with hydrazones: Libraries incorporating heterocyclic and steroidal motifs
Simpson, Mark G.,Pittelkow, Michael,Watson, Stephen P.,Sanders, Jeremy K. M.
supporting information; experimental part, p. 1181 - 1187 (2010/06/13)
We expand the possibilities in hydrazone based dynamic combinatorial chemistry with a series of new building blocks incorporating heterocyclic motifs. The synthetic procedure allows efficient access to building blocks with the general structure (MeO)2CH-Heterocycle-C(O)NHNH2, originating from heterocycles with an amine and an ester functionality. The equilibrium distribution of macrocyclic N-acyl hydrazones formed upon deprotection of the building blocks with TFA in organic solvents is reported. The mixing behaviour of these heterocycle-based building blocks with our cholate-based building blocks is described, particularly the observation of kinetic intermediates that disappear following 'proof-reading'. The Royal Society of Chemistry.
HIV protease inhibitors useful for the treatment of aids
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, (2008/06/13)
[From equivalent EP0434365A2] Compounds of the form, A-G-B-B-J wherein A is an amine protecting group or urethane, G a dipeptide isostere substituted with a basic amine nitrogen, B an amino acid or analog thereof, and J a small terminal group are describe
