Search Results - "Bume, Desta"

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    Targeting a noncanonical, hairpin-containing G-quadruplex structure from the MYCN gene by Yang, Mo, Carter, Sakereh, Parmar, Shaifaly, Bume, Desta D, Calabrese, David R, Liang, Xiao, Yazdani, Kamyar, Xu, Man, Liu, Zhihui, Thiele, Carol J, Schneekloth, John S

    Published in Nucleic acids research (20-08-2021)
    “…Abstract The MYCN gene encodes the transcription factor N-Myc, a driver of neuroblastoma (NB). Targeting G-quadruplexes (G4s) with small molecules is…”
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    Journal Article
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    A chemical probe based on the PreQ1 metabolite enables transcriptome-wide mapping of binding sites by Balaratnam, Sumirtha, Rhodes, Curran, Bume, Desta Doro, Connelly, Colleen, Lai, Christopher C., Kelley, James A., Yazdani, Kamyar, Homan, Philip J., Incarnato, Danny, Numata, Tomoyuki, Schneekloth Jr, John S.

    Published in Nature communications (06-10-2021)
    “…The role of metabolite-responsive riboswitches in regulating gene expression in bacteria is well known and makes them useful systems for the study of RNA-small…”
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    Catalyzed and Promoted Aliphatic Fluorination by Bume, Desta Doro, Harry, Stefan Andrew, Lectka, Thomas, Pitts, Cody Ross

    Published in Journal of organic chemistry (17-08-2018)
    “…In the last six years, the direct functionalization of aliphatic C–H (and C–C) bonds through user-friendly, radical-based fluorination reactions has emerged as…”
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    Direct, visible light-sensitized benzylic C H fluorination of peptides using dibenzosuberenone: selectivity for phenylalanine-like residues by Bume, Desta Doro, Pitts, Cody Ross, Jokhai, Rayyan Trebonias, Lectka, Thomas

    Published in Tetrahedron (06-10-2016)
    “…A visible light-sensitized benzylic sp super(3) C--H fluorination protocol using dibenzosuberenone (5 mol %) and Selectfluor super( registered ) is optimized…”
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    Journal Article
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    Multiple Enone-Directed Reactivity Modes Lead to the Selective Photochemical Fluorination of Polycyclic Terpenoid Derivatives by Pitts, Cody Ross, Bume, Desta Doro, Harry, Stefan Andrew, Siegler, Maxime A, Lectka, Thomas

    Published in Journal of the American Chemical Society (15-02-2017)
    “…In the realm of aliphatic fluorination, the problem of reactivity has been very successfully addressed in recent years. In contrast, the associated problem of…”
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    Tandem C-C Bond Cleavage of ­Cyclopropanols and Oxidative Aromatization by Manganese(IV) Oxide in a Direct C-H to C-C Functionalization of Heteroaromatics by Bume, Desta Doro, Pitts, Cody Ross, Lectka, Thomas

    Published in European journal of organic chemistry (01-01-2016)
    “…We report a direct C–H to C–C bond functionalization of electron‐deficient heteroaromatics enabled by mild C–C bond cleavage of cyclopropanols as a new route…”
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    Sensitized Aliphatic Fluorination Directed by Terpenoidal Enones: A “Visible Light” Approach by Bume, Desta Doro, Harry, Stefan Andrew, Pitts, Cody Ross, Lectka, Thomas

    Published in Journal of organic chemistry (02-02-2018)
    “…In our continued effort to address the challenges of selective sp3 C–H fluorination on complex molecules, we report a sensitized aliphatic fluorination…”
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    Unstrained C-C bond activation and directed fluorination through photocatalytically-generated radical cations by Pitts, Cody Ross, Bloom, Michelle Sheanne, Bume, Desta Doro, Zhang, Qinze Arthur, Lectka, Thomas

    Published in Chemical science (Cambridge) (01-01-2015)
    “…Expanding the repertoire of controlled radical fluorination techniques, we present a photosensitized unstrained C-C bond activation/directed monofluorination…”
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    Ketones as directing groups in photocatalytic sp3 C-H fluorination by Bume, Desta Doro, Pitts, Cody Ross, Ghorbani, Fereshte, Harry, Stefan Andrew, Capilato, Joseph N, Siegler, Maxime A, Lectka, Thomas

    Published in Chemical science (Cambridge) (01-10-2017)
    “…The ubiquitous ketone carbonyl group generally deactivates substrates toward radical-based fluorinations, especially sites closest to it. Herein, ketones are…”
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    Site-Selective Approach to [beta]-Fluorination: Photocatalyzed Ring Opening of Cyclopropanols by Bloom, Steven, Bume, Desta Doro, Pitts, Cody Ross, Lectka, Thomas

    Published in Chemistry : a European journal (26-05-2015)
    “…To expand upon the recent pioneering reports of catalyzed sp3 CH fluorination methods, the next rational step is to focus on directing "radical-based…”
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    Site-Selective Approach to β-Fluorination: Photocatalyzed Ring Opening of Cyclopropanols by Bloom, Steven, Bume, Desta Doro, Pitts, Cody Ross, Lectka, Thomas

    Published in Chemistry : a European journal (26-05-2015)
    “…To expand upon the recent pioneering reports of catalyzed sp3 CH fluorination methods, the next rational step is to focus on directing “radical‐based…”
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    Journal Article
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    Fluorofunctionalization of CC Bonds with Selectfluor: Synthesis of β‑Fluoropiperazines through a Substrate-Guided Reactivity Switch by Capilato, Joseph N, Bume, Desta Doro, Lee, Wei Hao, Hoffenberg, Louis E. S, Jokhai, Rayyan Trebonias, Lectka, Thomas

    Published in Journal of organic chemistry (07-12-2018)
    “…The halofunctionalization of alkene substrates remains an essential tool for synthetic chemists. Herein, we report regioselective ammoniofluorination of…”
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    Direct, visible light-sensitized benzylic CH fluorination of peptides using dibenzosuberenone: selectivity for phenylalanine-like residues by Bume, Desta Doro, Pitts, Cody Ross, Jokhai, Rayyan Trebonias, Lectka, Thomas

    Published in Tetrahedron (06-10-2016)
    “…A visible light-sensitized benzylic sp3 CH fluorination protocol using dibenzosuberenone (5 mol %) and Selectfluor® is optimized for the direct…”
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    Journal Article
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    Ketones as directing groups in photocatalytic sp 3 C-H fluorination by Bume, Desta Doro, Pitts, Cody Ross, Ghorbani, Fereshte, Harry, Stefan Andrew, Capilato, Joseph N, Siegler, Maxime A, Lectka, Thomas

    Published in Chemical science (Cambridge) (01-10-2017)
    “…The ubiquitous ketone carbonyl group generally deactivates substrates toward radical-based fluorinations, especially sites closest to it. Herein, ketones are…”
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    Journal Article
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