| Literature DB >> 28450641 |
Daniel A DiRocco1, Yining Ji2, Edward C Sherer2, Artis Klapars2, Mikhail Reibarkh2, James Dropinski2, Rose Mathew2, Peter Maligres2, Alan M Hyde2, John Limanto2, Andrew Brunskill2, Rebecca T Ruck2, Louis-Charles Campeau2, Ian W Davies2.
Abstract
The catalytic stereoselective synthesis of compounds with chiral phosphorus centers remains an unsolved problem. State-of-the-art methods rely on resolution or stoichiometric chiral auxiliaries. Phosphoramidate prodrugs are a critical component of pronucleotide (ProTide) therapies used in the treatment of viral disease and cancer. Here we describe the development of a catalytic stereoselective method for the installation of phosphorus-stereogenic phosphoramidates to nucleosides through a dynamic stereoselective process. Detailed mechanistic studies and computational modeling led to the rational design of a multifunctional catalyst that enables stereoselectivity as high as 99:1.Entities:
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Year: 2017 PMID: 28450641 DOI: 10.1126/science.aam7936
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728