Search Results - "Knowles, R. R."
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Developing an ecological approach to physical activity promotion in adults with Cystic fibrosis
Published in PloS one (01-08-2022)“…There are few examples of interventions designed to promote physical activity (PA) in adults with Cystic fibrosis (CF). Increasing levels of habitual PA may be…”
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Synthetic Applications of Proton-Coupled Electron Transfer
Published in Accounts of chemical research (16-08-2016)“…Redox events in which an electron and proton are exchanged in a concerted elementary step are commonly referred to as proton-coupled electron transfers…”
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3
Catalytic generation of alkoxy radicals from unfunctionalized alcohols
Published in Chemical science (Cambridge) (07-11-2020)“…Alkoxy radicals have long been recognized as powerful synthetic intermediates with well-established reactivity patterns. Due to the high bond dissociation free…”
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Catalytic Alkene Carboaminations Enabled by Oxidative Proton-Coupled Electron Transfer
Published in Journal of the American Chemical Society (29-07-2015)“…Here we describe a dual catalyst system comprised of an iridium photocatalyst and weak phosphate base that is capable of both selectively homolyzing the N–H…”
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5
Ion-pair reorganization regulates reactivity in photoredox catalysts
Published in Nature chemistry (01-07-2022)“…Cyclometalated and polypyridyl complexes of d 6 metals are promising photoredox catalysts, using light to drive reactions with high kinetic or thermodynamic…”
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A Redox Strategy for Light-Driven, Out-of-Equilibrium Isomerizations and Application to Catalytic C–C Bond Cleavage Reactions
Published in Journal of the American Chemical Society (30-01-2019)“…We report a general protocol for the light-driven isomerization of cyclic aliphatic alcohols to linear carbonyl compounds. These reactions proceed via…”
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Catalytic alkylation of remote C–H bonds enabled by proton-coupled electron transfer
Published in Nature (London) (10-11-2016)“…Catalytic alkylation of C–H bonds is achieved via homolysis of N–H bonds of N -alkyl amides through proton-coupled electron transfer. Functionalizing…”
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Light - driven deracemization enabled by excited - state electron transfer
Published in Science (American Association for the Advancement of Science) (18-10-2019)“…Deracemization is an attractive strategy for asymmetric synthesis, but intrinsic energetic challenges have limited its development. Here, we report a…”
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Catalytic Ring-Opening of Cyclic Alcohols Enabled by PCET Activation of Strong O–H Bonds
Published in Journal of the American Chemical Society (31-08-2016)“…We report a new photocatalytic protocol for the redox-neutral isomerization of cyclic alcohols to linear ketones via C–C bond scission. Mechanistic studies…”
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1,3‐Alkyl Transposition in Allylic Alcohols Enabled by Proton‐Coupled Electron Transfer
Published in Angewandte Chemie International Edition (06-09-2021)“…A method is described for the isomerization of acyclic allylic alcohols into β‐functionalized ketones via 1,3‐alkyl transposition. This reaction proceeds via…”
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Enantioselective Synthesis of Pyrroloindolines via Noncovalent Stabilization of Indole Radical Cations and Applications to the Synthesis of Alkaloid Natural Products
Published in Journal of the American Chemical Society (07-03-2018)“…While interest in the synthetic chemistry of radical cations continues to grow, controlling enantioselectivity in the reactions of these intermediates remains…”
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12
Attractive noncovalent interactions in asymmetric catalysis: Links between enzymes and small molecule catalysts
Published in Proceedings of the National Academy of Sciences - PNAS (30-11-2010)“…Catalysis by neutral, organic, small molecules capable of binding and activating substrates solely via noncovalent interactions—particularly H-bonding—has…”
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Catalytic Ketyl-Olefin Cyclizations Enabled by Proton-Coupled Electron Transfer
Published in Journal of the American Chemical Society (10-07-2013)“…Concerted proton-coupled electron transfer is a key mechanism of substrate activation in biological redox catalysis. However, its applications in organic…”
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Catalytic Olefin Hydroamidation Enabled by Proton-Coupled Electron Transfer
Published in Journal of the American Chemical Society (28-10-2015)“…Here we report a ternary catalyst system for the intramolecular hydroamidation of unactivated olefins using simple N-aryl amide derivatives. Amide activation…”
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Photocatalytic Generation of Aminium Radical Cations for C─N Bond Formation
Published in ACS catalysis (16-10-2020)“…Aminium radical cations have been extensively studied as electrophilic aminating species that readily participate in C─N bond forming processes with alkenes…”
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Cryo-electron tomography reveals ciliary defects underlying human RSPH1 primary ciliary dyskinesia
Published in Nature communications (04-12-2014)“…Cilia play essential roles in normal human development and health; cilia dysfunction results in diseases such as primary ciliary dyskinesia (PCD). Despite…”
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Catalytic Hydroetherification of Unactivated Alkenes Enabled by Proton‐Coupled Electron Transfer
Published in Angewandte Chemie International Edition (13-07-2020)“…We report a catalytic, light‐driven method for the intramolecular hydroetherification of unactivated alkenols to furnish cyclic ether products. These reactions…”
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Photochemical and Electrochemical Applications of Proton-Coupled Electron Transfer in Organic Synthesis
Published in Chemical reviews (26-01-2022)“…We present here a review of the photochemical and electrochemical applications of multi-site proton-coupled electron transfer (MS-PCET) in organic synthesis…”
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Catalytic C–N Bond-Forming Reactions Enabled by Proton-Coupled Electron Transfer Activation of Amide N–H Bonds
Published in ACS catalysis (06-05-2016)“…Over the past three years, our group has become interested in the ability of proton-coupled electron transfer (PCET) to facilitate direct homolytic bond…”
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C–H Alkylation via Multisite-Proton-Coupled Electron Transfer of an Aliphatic C–H Bond
Published in Journal of the American Chemical Society (21-08-2019)“…The direct, site-selective alkylation of unactivated C(sp3)–H bonds in organic substrates is a long-standing goal in synthetic chemistry. General approaches…”
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