This submission belongs to the session a. General Organic Synthesis of the event The 4th International Electronic Conference on Synthetic Organic Chemistry
Published date
11 Sep, 2000
Citation
Paul R. Hanson, Kevin T. Sprott, Amino Acid-Derived Cyclic Phosphonamides as Potential HIV-Protease Inhibitors, in Proceedings of The 4th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2000, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-4-01866
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Amino Acid-Derived Cyclic Phosphonamides as Potential HIV-Protease Inhibitors
Kevin T. Sprott 1
Paul R. Hanson 1
1. Department of Chemistry, University of Kansas, Lawrence, KS 66045
Abstract
Phosphorus containing compounds have gained considerable attention due to their diverse biological and chemical profiles. A number of P-heterocycles have shown potent biological activity, and have become attractive targets as rationally designed small molecules. We are interested in continuing to build a library of highly functionalized heterocyclic phosphorus-containing compounds of varied chemical and biological interests. In out pursuit of novel P-heterocycles, we have recently become interested in the synthesis of amino acid-based phosphorus containing compounds that may have potentials as HIV-1 protease-inhibitors. Our efforts have largely been driven by the development of a number of cyclic urea-based HIV-1 protease inhibitors at Dupont-Merck that gave promising biological activity.
Keywords
n/a
A Chiral Silyl Ether as Auxiliary for the Asymmetric Nucleophilic Addition to a- and b-Silyloxy Carbonyl Compounds