254-86-4Relevant articles and documents
Annelated Pyridine Bases for the Selective Acylation of 1,2-Diols
Mayr, Stefanie,Zipse, Hendrik
supporting information, (2022/03/08)
A set of 24 annelated derivatives of 4-diaminopyridine (DMAP) has been synthesized and tested with respect to its catalytic potential in the regioselective acylation of 1,2-diol substrates. The Lewis basicities of the catalysts as quantified through quantum chemical calculations vary due to inductive substituent effects and intramolecular stacking interactions between side chain π-systems and the pyridinium core ring system. The primary over secondary hydroxyl group selectivities in catalytic acylations of 1,2-diol substrates depend on the size and the steric demand of the Lewis base and the anhydride reagent.
SUBSTITUTED CYCLIC COMPOUNDS AND METHODS OF USE
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Paragraph 0302, (2014/06/24)
The present invention provides novel substituted alkynyl compounds, pharmaceutical acceptable salts and formulations thereof useful in modulating the protein tyrosine kinase activity, and in modulating cellular activities such as proliferation, differentiation, apoptosis, migration and invasion. The invention also provides pharmaceutically acceptable compositions comprising such compounds and methods of using the compositions in the treatment of hyperproliferative disorders in mammals, especially humans.
Annelated pyridines as highly nucleophilic and Lewis basic catalysts for acylation reactions
Tandon, Raman,Unzner, Teresa,Nigst, Tobias A.,De Rycke, Nicolas,Mayer, Peter,Wendt, Bernd,David, Olivier R. P.,Zipse, Hendrik
supporting information, p. 6435 - 6442 (2013/07/05)
New heterocyclic derivatives of 9-azajulolidine have been synthesized and characterized with respect to their nucleophilicity and Lewis basicity. The Lewis basicity of these bases as quantified through their theoretically calculated methyl-cation affinities correlate well with the experimentally measured reaction rates for addition to benzhydryl cations. All newly synthesized pyridines show exceptional catalytic activities in benchmark acylation reactions, which correlate only poorly with Lewis basicity or nucleophilicity parameters. A combination of Lewis basicity with charge and geometric parameters in the framework of a three-component quantitative structure-activity relationship (QSAR) model is, however, highly predictive. Copyright