Year |
Citation |
Score |
2024 |
Liu Y, Bender SG, Sorigue D, Diaz DJ, Ellington AD, Mann G, Allmendinger S, Hyster TK. Asymmetric Synthesis of α-Chloroamides via Photoenzymatic Hydroalkylation of Olefins. Journal of the American Chemical Society. PMID 38442365 DOI: 10.1021/jacs.4c00927 |
0.335 |
|
2023 |
Clements HD, Flynn AR, Nicholls BT, Grosheva D, Lefave SJ, Merriman MT, Hyster TK, Sigman MS. Using Data Science for Mechanistic Insights and Selectivity Predictions in a Non-Natural Biocatalytic Reaction. Journal of the American Chemical Society. PMID 37530568 DOI: 10.1021/jacs.3c03639 |
0.302 |
|
2023 |
Ouyang Y, Turek-Herman J, Qiao T, Hyster TK. Asymmetric Carbohydroxylation of Alkenes Using Photoenzymatic Catalysis. Journal of the American Chemical Society. PMID 37498747 DOI: 10.1021/jacs.3c06618 |
0.437 |
|
2023 |
Li X, Page CG, Zanetti-Polzi L, Kalra AP, Oblinsky DG, Daidone I, Hyster TK, Scholes GD. Mechanism and Dynamics of Photodecarboxylation Catalyzed by Lactate Monooxygenase. Journal of the American Chemical Society. 145: 13232-13240. PMID 37289179 DOI: 10.1021/jacs.3c02446 |
0.35 |
|
2023 |
Page CG, Cao J, Oblinsky DG, MacMillan SN, Dahagam S, Lloyd RM, Charnock SJ, Scholes GD, Hyster TK. Regioselective Radical Alkylation of Arenes Using Evolved Photoenzymes. Journal of the American Chemical Society. PMID 37199445 DOI: 10.1021/jacs.3c03607 |
0.416 |
|
2023 |
Hyster T, Page C, Cao J, Oblinsky D, MacMillan S, Dahagam S, Lloyd R, Charnock S, Scholes G. Regioselective Radical Alkylation of Arenes Using Evolved Photoenzymes. Research Square. PMID 36865242 DOI: 10.21203/rs.3.rs-2602958/v1 |
0.428 |
|
2023 |
Fu H, Qiao T, Carceller JM, MacMillan SN, Hyster TK. Asymmetric -Alkylation of Nitroalkanes Enzymatic Photoredox Catalysis. Journal of the American Chemical Society. 145: 787-793. PMID 36608280 DOI: 10.1021/jacs.2c12197 |
0.434 |
|
2022 |
Nicholls BT, Qiao T, Hyster TK. A Photoenzyme for Challenging Lactam Radical Cyclizations. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 33: 1204-1208. PMID 37876576 |
0.366 |
|
2022 |
Laguerre N, Riehl PS, Oblinsky DG, Emmanuel MA, Black MJ, Scholes GD, Hyster TK. Radical Termination via β-Scission Enables Photoenzymatic Allylic Alkylation Using "Ene"-Reductases. Acs Catalysis. 12: 9801-9805. PMID 37859751 DOI: 10.1021/acscatal.2c02294 |
0.339 |
|
2022 |
Ye Y, Cao J, Oblinsky DG, Verma D, Prier CK, Scholes GD, Hyster TK. Using enzymes to tame nitrogen-centred radicals for enantioselective hydroamination. Nature Chemistry. PMID 36376390 DOI: 10.1038/s41557-022-01083-z |
0.425 |
|
2022 |
Fu H, Cao J, Qiao T, Qi Y, Charnock SJ, Garfinkle S, Hyster TK. An Asymmetric sp-sp Cross-Electrophile Coupling Using 'Ene'-Reductases. Nature. PMID 35952713 DOI: 10.1038/s41586-022-05167-1 |
0.438 |
|
2021 |
Gao X, Turek-Herman JR, Choi YJ, Cohen RD, Hyster TK. Photoenzymatic Synthesis of α-Tertiary Amines by Engineered Flavin-Dependent "Ene"-Reductases. Journal of the American Chemical Society. PMID 34784482 DOI: 10.1021/jacs.1c09828 |
0.372 |
|
2021 |
Fu H, Lam H, Emmanuel MA, Kim JH, Sandoval BA, Hyster TK. Ground-State Electron Transfer as an Initiation Mechanism for Biocatalytic C-C Bond Forming Reactions. Journal of the American Chemical Society. PMID 34114803 DOI: 10.1021/jacs.1c04334 |
0.423 |
|
2021 |
Ye Y, Fu H, Hyster TK. Activation modes in biocatalytic radical cyclization reactions. Journal of Industrial Microbiology & Biotechnology. PMID 33674826 DOI: 10.1093/jimb/kuab021 |
0.33 |
|
2020 |
Page CG, Cooper SJ, DeHovitz JS, Oblinsky DG, Biegasiewicz KF, Antropow AH, Armbrust KW, Ellis JM, Hamann LG, Horn EJ, Oberg KM, Scholes GD, Hyster TK. Quaternary Charge-Transfer Complex Enables Photoenzymatic Intermolecular Hydroalkylation of Olefins. Journal of the American Chemical Society. PMID 33369395 DOI: 10.1021/jacs.0c11462 |
0.766 |
|
2020 |
Clayman PD, Hyster TK. Photoenzymatic Generation of Unstabilized Alkyl Radicals: An Asymmetric Reductive Cyclization. Journal of the American Chemical Society. PMID 32857506 DOI: 10.1021/Jacs.0C07918 |
0.303 |
|
2020 |
DeHovitz JS, Loh YY, Kautzky JA, Nagao K, Meichan AJ, Yamauchi M, MacMillan DWC, Hyster TK. Static to inducibly dynamic stereocontrol: The convergent use of racemic β-substituted ketones. Science (New York, N.Y.). 369: 1113-1118. PMID 32855338 DOI: 10.1126/Science.Abc9909 |
0.362 |
|
2020 |
Hyster T, Nakano Y, Black MJ, Meichan AJ, Sandoval BA, Chung M, Biegasiewicz K, Zhu T. Photoenzymatic Hydrogenation of Heteroaromatic Olefins using 'Ene'-Reductases with Photoredox Catalysts. Angewandte Chemie (International Ed. in English). PMID 32181943 DOI: 10.1002/Anie.202003125 |
0.47 |
|
2020 |
Sandoval BA, Hyster TK. Emerging strategies for expanding the toolbox of enzymes in biocatalysis. Current Opinion in Chemical Biology. 55: 45-51. PMID 31935627 DOI: 10.1016/J.Cbpa.2019.12.006 |
0.44 |
|
2020 |
Hyster TK. Cluster Preface: Biocatalysis Synlett. 31: 223-223. DOI: 10.1055/S-0039-1691581 |
0.359 |
|
2020 |
Hyster TK. Radical Biocatalysis: Using Non-Natural Single Electron Transfer Mechanisms to Access New Enzymatic Functions Synlett. 31: 248-254. DOI: 10.1055/S-0037-1611818 |
0.48 |
|
2019 |
Black MJ, Biegasiewicz KF, Meichan AJ, Oblinsky DG, Kudisch B, Scholes GD, Hyster TK. Asymmetric redox-neutral radical cyclization catalysed by flavin-dependent 'ene'-reductases. Nature Chemistry. PMID 31792387 DOI: 10.1038/S41557-019-0370-2 |
0.521 |
|
2019 |
Biegasiewicz KF, Cooper SJ, Gao X, Oblinsky DG, Kim JH, Garfinkle SE, Joyce LA, Sandoval BA, Scholes GD, Hyster TK. Photoexcitation of flavoenzymes enables a stereoselective radical cyclization. Science (New York, N.Y.). 364: 1166-1169. PMID 31221855 DOI: 10.1126/Science.Aaw1143 |
0.658 |
|
2019 |
Hyster T, Sandoval B, Kurtoic S, Chung M, Biegasiewicz K. Photoenzymatic Catalysis Enables Radical- Mediated Ketone Reduction in 'Ene'-Reductases. Angewandte Chemie (International Ed. in English). PMID 30951226 DOI: 10.1002/Anie.201902005 |
0.519 |
|
2018 |
Hyster TK, Dalton DM, Rovis T. Correction: Ligand design for Rh(iii)-catalyzed C-H activation: an unsymmetrical cyclopentadienyl group enables a regioselective synthesis of dihydroisoquinolones. Chemical Science. 9: 8024. PMID 30542552 DOI: 10.1039/C8Sc90195C |
0.762 |
|
2018 |
Nakano Y, Biegasiewicz KF, Hyster TK. Biocatalytic hydrogen atom transfer: an invigorating approach to free-radical reactions. Current Opinion in Chemical Biology. 49: 16-24. PMID 30269010 DOI: 10.1016/J.Cbpa.2018.09.001 |
0.449 |
|
2018 |
Biegasiewicz KF, Cooper SJ, Emmanuel MA, Miller DC, Hyster TK. Catalytic promiscuity enabled by photoredox catalysis in nicotinamide-dependent oxidoreductases. Nature Chemistry. PMID 29892028 DOI: 10.1038/S41557-018-0059-Y |
0.655 |
|
2017 |
Hyster TK, Dalton DM, Rovis T. Correction: Ligand design for Rh(iii)-catalyzed C-H activation: an unsymmetrical cyclopentadienyl group enables a regioselective synthesis of dihydroisoquinolones. Chemical Science. 8: 1666. PMID 30123475 DOI: 10.1039/c6sc90080a |
0.757 |
|
2017 |
Sandoval BA, Meichan AJ, Hyster TK. Enantioselective Hydrogen Atom Transfer: Discovery of Catalytic Promiscuity in Flavin-Dependent 'Ene'-Reductases. Journal of the American Chemical Society. PMID 28780870 DOI: 10.1021/Jacs.7B05468 |
0.396 |
|
2016 |
Emmanuel MA, Greenberg NR, Oblinsky DG, Hyster TK. Accessing non-natural reactivity by irradiating nicotinamide-dependent enzymes with light. Nature. 540: 414-417. PMID 27974767 DOI: 10.1038/Nature20569 |
0.471 |
|
2016 |
Hyster TK, Ward TR. Genetic Optimization of Metalloenzymes: Enhancing Enzymes for Non-Natural Reactions. Angewandte Chemie (International Ed. in English). PMID 26971363 DOI: 10.1002/Anie.201508816 |
0.362 |
|
2016 |
Prier CK, Hyster TK, Farwell CC, Huang A, Arnold FH. Asymmetric Enzymatic Synthesis of Allylic Amines: A Sigmatropic Rearrangement Strategy. Angewandte Chemie (International Ed. in English). PMID 26970325 DOI: 10.1002/Anie.201601056 |
0.776 |
|
2015 |
Farwell CC, Zhang RK, McIntosh JA, Hyster TK, Arnold FH. Enantioselective Enzyme-Catalyzed Aziridination Enabled by Active-Site Evolution of a Cytochrome P450. Acs Central Science. 1: 89-93. PMID 26405689 DOI: 10.1021/Acscentsci.5B00056 |
0.768 |
|
2015 |
Hyster TK, Rovis T. Correction: Pyridine synthesis from oximes and alkynes via rhodium(III) catalysis: Cp* and Cp(t) provide complementary selectivity. Chemical Communications (Cambridge, England). 51: 5778. PMID 25749239 DOI: 10.1039/c5cc90120k |
0.535 |
|
2015 |
Hyster TK, Dalton DM, Rovis T. Ligand Design for Rh(III)-Catalyzed C-H Activation: An Unsymmetrical Cyclopentadienyl Enables a Regioselective Synthesis of Dihydroisoquinolones. Chemical Science (Royal Society of Chemistry : 2010). 6: 254-258. PMID 25489470 DOI: 10.1039/C4Sc02590C |
0.762 |
|
2015 |
Hyster TK. High-Valent Co(III)- and Ni(II)-Catalyzed C–H Activation Catalysis Letters. 145: 458-467. DOI: 10.1007/S10562-014-1449-4 |
0.378 |
|
2015 |
Hyster TK, Arnold FH. P450BM3-axial mutations: A gateway to non-natural reactivity Israel Journal of Chemistry. 55: 14-20. DOI: 10.1002/Ijch.201400080 |
0.619 |
|
2015 |
Hyster TK. ChemInform Abstract: High-Valent Co(III)- and Ni(II)-Catalyzed C-H Activation Cheminform. 46: no-no. DOI: 10.1002/CHIN.201513314 |
0.31 |
|
2014 |
Hyster TK, Farwell CC, Buller AR, McIntosh JA, Arnold FH. Enzyme-controlled nitrogen-atom transfer enables regiodivergent C-H amination. Journal of the American Chemical Society. 136: 15505-8. PMID 25325618 DOI: 10.1021/Ja509308V |
0.748 |
|
2014 |
Farwell CC, McIntosh JA, Hyster TK, Wang ZJ, Arnold FH. Enantioselective imidation of sulfides via enzyme-catalyzed intermolecular nitrogen-atom transfer. Journal of the American Chemical Society. 136: 8766-71. PMID 24901646 DOI: 10.1021/Ja503593N |
0.782 |
|
2013 |
Hyster TK, Rovis T. Rhodium(III)-Catalyzed C-H Activation Mediated Synthesis of Isoquinolones from Amides and Cyclopropenes. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 24: 1842-1844. PMID 25346576 DOI: 10.1055/S-0033-1339510 |
0.658 |
|
2013 |
Davis TA, Hyster TK, Rovis T. Rhodium(III)-catalyzed intramolecular hydroarylation, amidoarylation, and Heck-type reaction: three distinct pathways determined by an amide directing group. Angewandte Chemie (International Ed. in English). 52: 14181-5. PMID 24214733 DOI: 10.1002/Anie.201307631 |
0.723 |
|
2013 |
Hyster TK, Ruhl KE, Rovis T. A coupling of benzamides and donor/acceptor diazo compounds to form γ-lactams via Rh(III)-catalyzed C-H activation. Journal of the American Chemical Society. 135: 5364-7. PMID 23548055 DOI: 10.1021/Ja402274G |
0.615 |
|
2012 |
Hyster TK, Knörr L, Ward TR, Rovis T. Biotinylated Rh(III) complexes in engineered streptavidin for accelerated asymmetric C-H activation. Science (New York, N.Y.). 338: 500-3. PMID 23112327 DOI: 10.1126/Science.1226132 |
0.663 |
|
2011 |
Hyster TK, Rovis T. An Improved Catalyst Architecture for Rhodium (III) Catalyzed C-H Activation and its Application to Pyridone Synthesis. Chemical Science (Royal Society of Chemistry : 2010). 2: 1606-1610. PMID 25580208 DOI: 10.1039/C1Sc00235J |
0.642 |
|
2011 |
Du Y, Hyster TK, Rovis T. Rhodium(III)-catalyzed oxidative carbonylation of benzamides with carbon monoxide. Chemical Communications (Cambridge, England). 47: 12074-6. PMID 22006288 DOI: 10.1039/C1Cc15843K |
0.663 |
|
2011 |
Hyster TK, Rovis T. Pyridine synthesis from oximes and alkynes via rhodium(III) catalysis: Cp* and Cp(t) provide complementary selectivity. Chemical Communications (Cambridge, England). 47: 11846-8. PMID 21986995 DOI: 10.1039/C1Cc15248C |
0.605 |
|
2011 |
Du Y, Hyster TK, Rovis T. Rhodium-catalyzed oxidative carbonylation of benzamides with CO under mild conditions Acs National Meeting Book of Abstracts. |
0.48 |
|
2010 |
Hyster TK, Rovis T. Rhodium-catalyzed oxidative cycloaddition of benzamides and alkynes via C-H/N-H activation. Journal of the American Chemical Society. 132: 10565-9. PMID 20662529 DOI: 10.1021/Ja103776U |
0.661 |
|
2009 |
Wentzel MT, Reddy VJ, Hyster TK, Douglas CJ. Chemoselectivity in catalytic C-C and C-H bond activation: controlling intermolecular carboacylation and hydroarylation of alkenes. Angewandte Chemie (International Ed. in English). 48: 6121-3. PMID 19591181 DOI: 10.1002/Anie.200902215 |
0.627 |
|
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