Abstract
An efficient method for the solution-phase parallel synthesis of 4-substituted-1,4-dihydroisoquinolin-3-ones is developed. The isoquinolinones were constructed employing an intramolecular Heck reaction, providing full regio- and stereoselectivity. Most of the synthesized compounds showed potent antiproliferative activities against tumor cell lines.
Publication types
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Evaluation Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Antiprotozoal Agents / chemical synthesis
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Antiprotozoal Agents / chemistry
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Antiprotozoal Agents / pharmacology*
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Cell Line, Tumor
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Cell Proliferation / drug effects
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Combinatorial Chemistry Techniques
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Drug Screening Assays, Antitumor
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Humans
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Isoquinolines / chemical synthesis
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Isoquinolines / chemistry
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Isoquinolines / pharmacology*
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Molecular Structure
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Small Molecule Libraries
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Stereoisomerism
Substances
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Antiprotozoal Agents
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Isoquinolines
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Small Molecule Libraries