Search Results - "Prier, Christopher K"
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Chemomimetic Biocatalysis: Exploiting the Synthetic Potential of Cofactor-Dependent Enzymes To Create New Catalysts
Published in Journal of the American Chemical Society (11-11-2015)“…Despite the astonishing breadth of enzymes in nature, no enzymes are known for many of the valuable catalytic transformations discovered by chemists. Recent…”
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Enantioselective Aminohydroxylation of Styrenyl Olefins Catalyzed by an Engineered Hemoprotein
Published in Angewandte Chemie International Edition (04-03-2019)“…Chiral 1,2‐amino alcohols are widely represented in biologically active compounds from neurotransmitters to antivirals. While many synthetic methods have been…”
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Stereoselective Enzymatic Synthesis of Heteroatom-Substituted Cyclopropanes
Published in ACS catalysis (06-04-2018)“…The repurposing of hemoproteins for non-natural carbene transfer activities has generated enzymes for functions previously accessible only to chemical…”
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Asymmetric Enzymatic Synthesis of Allylic Amines: A Sigmatropic Rearrangement Strategy
Published in Angewandte Chemie International Edition (04-04-2016)“…Sigmatropic rearrangements, while rare in biology, offer opportunities for the efficient and selective synthesis of complex chemical motifs. A “P411”…”
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5
Recent preparative applications of redox enzymes
Published in Current opinion in chemical biology (01-04-2019)“…Redox enzymes offer many powerful transformations for the efficient industrial-scale synthesis of diverse chemicals desired by society. Here we survey recent…”
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6
Visible Light Photoredox Catalysis with Transition Metal Complexes: Applications in Organic Synthesis
Published in Chemical reviews (10-07-2013)“…Prier et al examine visible light photoredox catalysis with transition metal complexes with regard to applications in organic synthesis…”
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Enantioselective, intermolecular benzylic C–H amination catalysed by an engineered iron-haem enzyme
Published in Nature chemistry (01-07-2017)“…C–H bonds are ubiquitous structural units of organic molecules. Although these bonds are generally considered to be chemically inert, the recent emergence of…”
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Discovery of an α-Amino C-H Arylation Reaction Using the Strategy of Accelerated Serendipity
Published in Science (American Association for the Advancement of Science) (25-11-2011)“…Serendipity has long been a welcome yet elusive phenomenon in the advancement of chemistry. We sought to exploit serendipity as a means of rapidly identifying…”
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Amine α-heteroarylation via photoredox catalysis: a homolytic aromatic substitution pathway
Published in Chemical science (Cambridge) (01-11-2014)“…The direct α-heteroarylation of tertiary amines has been accomplished photoredox catalysis to generate valuable benzylic amine pharmacophores. A variety of…”
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10
Expanding the scope of the Cu assisted Suzuki–Miyaura reaction
Published in Tetrahedron letters (28-09-2011)“…Recent advances in the development of the copper facilitated Suzuki–Miyaura reaction are described. Improvements include expansion of substrate scope to…”
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Using enzymes to tame nitrogen-centred radicals for enantioselective hydroamination
Published in Nature chemistry (01-02-2023)“…The formation of C–N bonds—of great importance to the pharmaceutical industry—can be facilitated enzymatically using nucleophilic and nitrene transfer…”
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12
Enantioselective Aminohydroxylation of Styrenyl Olefins Catalyzed by an Engineered Hemoprotein
Published in Angewandte Chemie (04-03-2019)“…Chiral 1,2‐amino alcohols are widely represented in biologically active compounds from neurotransmitters to antivirals. While many synthetic methods have been…”
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13
Stereodivergent Synthesis of 3‐Hydroxyprolines and 3‐Hydroxypipecolic Acids via Ketoreductase‐Catalyzed Dynamic Kinetic Reduction
Published in Advanced synthesis & catalysis (19-11-2019)“…We report a practical enzymatic approach for the stereoselective synthesis of hydroxylated cyclic amino acids. Using ketoreductases, cyclic ketoesters are…”
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14
Facile Ring-Opening of Azabicyclic [3.1.0]- and [4.1.0]Aminocyclopropanes to Afford 3-Piperidinone and 3-Azepinone
Published in Organic letters (04-03-2011)“…Azabicyclic [3.1.0] and [4.1.0] Kulinkovich products underwent a facile reduction/fragmentation to afford a variety of 3-piperidinones and 3-azepinones,…”
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15
Asymmetric Enzymatic Synthesis of Allylic Amines: A Sigmatropic Rearrangement Strategy
Published in Angewandte Chemie (04-04-2016)“…Sigmatropic rearrangements, while rare in biology, offer opportunities for the efficient and selective synthesis of complex chemical motifs. A “P411”…”
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16
Enzymes for amino acid synthesis by design
Published in Nature catalysis (01-05-2021)“…Creating enzymes with new capabilities is a key goal for synthetic biology and sustainable chemistry. Now, computational approaches have been used to quickly…”
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Use of a Dynamic Flow Platform To Translate a Batch Immobilized Transaminase Process to a Packed Bed Reactor for the Synthesis of an Intermediate of Nemtabrutinib
Published in Organic process research & development (17-05-2024)“…Herein we describe the translation of an immobilized transaminase process in batch to a packed bed reactor for the synthesis of cyrene amine, an intermediate…”
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Amine α-heteroarylation via photoredox catalysis: a homolytic aromatic substitution pathwayElectronic supplementary information (ESI) available: Experimental procedures, structural proofs, and spectral data for all new compounds are provided (97 pages) (PDF). See DOI: 10.1039/c4sc02155j
Published 29-09-2014“…The direct α-heteroarylation of tertiary amines has been accomplished via photoredox catalysis to generate valuable benzylic amine pharmacophores. A variety of…”
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Amination of a Green Solvent via Immobilized Biocatalysis for the Synthesis of Nemtabrutinib
Published in ACS catalysis (16-06-2023)“…Enzymes are capable of unique and selective transformations that can enable efficient chemical production. While many industrial processes have been developed…”
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Enantioselective, Intermolecular Benzylic C–H Amination Catalyzed by an Engineered Iron-Heme Enzyme
Published in Nature chemistry (29-05-2017)“…C–H bonds are ubiquitous structural units of organic molecules; while these bonds are generally considered to be chemically inert, the recent emergence of…”
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