TY  - UNPB
ID  - pittir10304
UR  - http://d-scholarship-dev.library.pitt.edu/10304/
A1  - Arnold, David Matthew
TI  - Synthesis of Biologically Active Heterocycles and Development of New Organometallic Methodologies
Y1  - 2011/01/27/
N2  - The study of the synthesis of highly functionalized heterocyclic compounds represents an important subset of synthetic organic transformations leading to target compounds with a wide set of applications in medicinal chemistry, biological chemistry, materials sciences and natural product synthesis. Through this work, synthetic strategies leading to a novel set of ester linked substituted quinoline - uracil scaffolds have been developed and the resulting products were found to be inhibitors of MPK1, an important target in cancer research. This work has also led to the development and implementation of novel synthetic strategies toward highly functionalized, traditionally pharmacologically important 6-amino-, 6-hydroxy- and 6-oxo-uracil and 4,6-dihydroxypiperidone scaffolds. A novel Plk1-PBD inhibitor from this series would be important to probe the mechanism of this enzyme during mitosis and to develop a clinical candidate for this validated cancer target. The Plk1-PBD research endeavor also documents a case for a tandem synthetic/analytical structure determination study. The structure of an initially elusive compound from a high throughput screening of 97,090 compounds was determined by this approach. Finally, the utility of novel heterocyclic sulfonyl and sulfinyl nitrogen protecting groups has been demonstrated through the addition of organometallic reagents to 2-methylthiadiazole-, 2-benzothiazolesulfonylbenzaldimines and 2-pyridylsulfinylbenzaldimines. It was found that these addition reactions proceeded with a variety of organometallic nucleophiles including Gringnard reagents, organozinc and organocuprates. The heterocyclic sulfonyl protecting groups were easily cleaved from the ?-branched amines, affording a useful protecting group strategy for the synthesis of this important class of compounds.
AV  - public
KW  - anticancer drug target; heterocycle synthesis; imines; inhibitor synthesis; library synthesis; medicinal chemistry; organometallic chemistry; polo-box domain; polo-like kinases; probe development; quinolines; screening artifact; uracils; mitogen-activated protein kinase phosphatases-1; piperidones
ER  -