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  1. Article: Nature Chose Phosphates and Chemists Should Too: How Emerging P(V) Methods Can Augment Existing Strategies.

    Knouse, Kyle W / Flood, Dillon T / Vantourout, Julien C / Schmidt, Michael A / Mcdonald, Ivar M / Eastgate, Martin D / Baran, Phil S

    ACS central science

    2021  Volume 7, Issue 9, Page(s) 1473–1485

    Abstract: Phosphate linkages govern life as we know it. Their unique properties provide the foundation for many natural systems from cell biology and biosynthesis to the backbone of nucleic acids. Phosphates are ideal natural moieties; existing as ionized species ... ...

    Abstract Phosphate linkages govern life as we know it. Their unique properties provide the foundation for many natural systems from cell biology and biosynthesis to the backbone of nucleic acids. Phosphates are ideal natural moieties; existing as ionized species in a stable P(V)-oxidation state, they are endowed with high stability but exhibit enzymatically unlockable potential. Despite intense interest in phosphorus catalysis and condensation chemistry, organic chemistry has not fully embraced the potential of P(V) reagents. To be sure, within the world of chemical oligonucleotide synthesis, modern approaches utilize P(III) reagent systems to create phosphate linkages and their analogs. In this Outlook, we present recent studies from our laboratories suggesting that numerous exciting opportunities for P(V) chemistry exist at the nexus of organic synthesis and biochemistry. Applications to the synthesis of stereopure antisense oligonucleotides, cyclic dinucleotides, methylphosphonates, and phosphines are reviewed as well as chemoselective modification to peptides, proteins, and nucleic acids. Finally, an outlook into what may be possible in the future with P(V) chemistry is previewed, suggesting these examples represent just the tip of the iceberg.
    Language English
    Publishing date 2021-09-10
    Publishing country United States
    Document type Journal Article ; Review
    ISSN 2374-7943
    ISSN 2374-7943
    DOI 10.1021/acscentsci.1c00487
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Unlocking P(V): Reagents for chiral phosphorothioate synthesis.

    Knouse, Kyle W / deGruyter, Justine N / Schmidt, Michael A / Zheng, Bin / Vantourout, Julien C / Kingston, Cian / Mercer, Stephen E / Mcdonald, Ivar M / Olson, Richard E / Zhu, Ye / Hang, Chao / Zhu, Jason / Yuan, Changxia / Wang, Qinggang / Park, Peter / Eastgate, Martin D / Baran, Phil S

    Science (New York, N.Y.)

    2018  Volume 361, Issue 6408, Page(s) 1234–1238

    Abstract: Phosphorothioate nucleotides have emerged as powerful pharmacological substitutes of their native phosphodiester analogs with important translational applications in antisense oligonucleotide (ASO) therapeutics and cyclic dinucleotide (CDN) synthesis. ... ...

    Abstract Phosphorothioate nucleotides have emerged as powerful pharmacological substitutes of their native phosphodiester analogs with important translational applications in antisense oligonucleotide (ASO) therapeutics and cyclic dinucleotide (CDN) synthesis. Stereocontrolled installation of this chiral motif has long been hampered by the systemic use of phosphorus(III) [P(III)]-based reagent systems as the sole practical means of oligonucleotide assembly. A fundamentally different approach is described herein: the invention of a P(V)-based reagent platform for programmable, traceless, diastereoselective phosphorus-sulfur incorporation. The power of this reagent system is demonstrated through the robust and stereocontrolled synthesis of various nucleotidic architectures, including ASOs and CDNs, via an efficient, inexpensive, and operationally simple protocol.
    MeSH term(s) Genetic Therapy ; Isomerism ; Nucleotides/chemistry ; Phosphorothioate Oligonucleotides/chemical synthesis ; Phosphorothioate Oligonucleotides/chemistry ; Phosphorothioate Oligonucleotides/therapeutic use ; Sulfur/chemistry
    Chemical Substances Nucleotides ; Phosphorothioate Oligonucleotides ; Sulfur (70FD1KFU70)
    Language English
    Publishing date 2018-08-02
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 128410-1
    ISSN 1095-9203 ; 0036-8075
    ISSN (online) 1095-9203
    ISSN 0036-8075
    DOI 10.1126/science.aau3369
    Database MEDical Literature Analysis and Retrieval System OnLINE

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