Year |
Citation |
Score |
2023 |
Stout CN, Wasfy NM, Chen F, Renata H. Charting the Evolution of Chemoenzymatic Strategies in the Syntheses of Complex Natural Products. Journal of the American Chemical Society. 145: 18161-18181. PMID 37553092 DOI: 10.1021/jacs.3c03422 |
0.374 |
|
2023 |
Amatuni A, Shuster A, Abegg D, Adibekian A, Renata H. Comprehensive Structure-Activity Relationship Studies of Cepafungin Enabled by Biocatalytic C-H Oxidations. Acs Central Science. 9: 239-251. PMID 36844499 DOI: 10.1021/acscentsci.2c01219 |
0.314 |
|
2022 |
Li J, Chen F, Renata H. Concise Chemoenzymatic Synthesis of Gedunin. Journal of the American Chemical Society. PMID 36222746 DOI: 10.1021/jacs.2c09048 |
0.358 |
|
2022 |
Li F, Deng H, Renata H. Remote B-Ring Oxidation of Sclareol with an Engineered P450 Facilitates Divergent Access to Complex Terpenoids. Journal of the American Chemical Society. 144: 7616-7621. PMID 35452234 DOI: 10.1021/jacs.2c02958 |
0.788 |
|
2021 |
Li F, Renata H. A Chiral-Pool-Based Strategy to Access -Fused Drimane Meroterpenoids: Chemoenzymatic Total Syntheses of Polysin, -Acetyl-polyveoline and the Chrodrimanins. Journal of the American Chemical Society. PMID 34670085 DOI: 10.1021/jacs.1c08696 |
0.775 |
|
2021 |
Renata H. Exploration of Iron- and a-Ketoglutarate-Dependent Dioxygenases as Practical Biocatalysts in Natural Product Synthesis. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 32: 775-784. PMID 34413574 DOI: 10.1055/s-0040-1707320 |
0.319 |
|
2021 |
Renata H, Shimizu E, Zwick CR. Regiodivergent Biocatalytic Hydroxylation of L-Glutamine Facilitated by Characterization of Non-Heme Dioxygenases from Non-Ribosomal Peptide Biosyntheses. Tetrahedron. 90. PMID 34366493 DOI: 10.1016/j.tet.2021.132190 |
0.366 |
|
2021 |
Li F, Yang LC, Zhang J, Chen J, Renata H. Stereoselective Synthesis of b-Branched Aromatic a-Amino Acids via Biocatalytic Dynamic Kinetic Resolution. Angewandte Chemie (International Ed. in English). PMID 34056805 DOI: 10.1002/anie.202105656 |
0.756 |
|
2021 |
Renata H. Synthetic utility of oxygenases in site-selective terpenoid functionalization. Journal of Industrial Microbiology & Biotechnology. PMID 33928356 DOI: 10.1093/jimb/kuab002 |
0.363 |
|
2021 |
Stout CN, Renata H. Reinvigorating the Chiral Pool: Chemoenzymatic Approaches to Complex Peptides and Terpenoids. Accounts of Chemical Research. PMID 33543931 DOI: 10.1021/acs.accounts.0c00823 |
0.439 |
|
2021 |
Zwick CR, Sosa MB, Renata H. Modular Chemoenzymatic Synthesis of GE81112 B1 and Related Analogues Enables Elucidation of Its Key Pharmacophores. Journal of the American Chemical Society. PMID 33416325 DOI: 10.1021/jacs.0c13424 |
0.358 |
|
2020 |
Zhang X, King-Smith E, Dong LB, Yang LC, Rudolf JD, Shen B, Renata H. Divergent synthesis of complex diterpenes through a hybrid oxidative approach. Science (New York, N.Y.). 369: 799-806. PMID 32792393 DOI: 10.1126/Science.Abb8271 |
0.479 |
|
2020 |
Amatuni A, Shuster A, Adibekian A, Renata H. Concise Chemoenzymatic Total Synthesis and Identification of Cellular Targets of Cepafungin I. Cell Chemical Biology. PMID 32763140 DOI: 10.1016/J.Chembiol.2020.07.012 |
0.453 |
|
2020 |
Li J, Amatuni A, Renata H. Recent advances in the chemoenzymatic synthesis of bioactive natural products. Current Opinion in Chemical Biology. 55: 111-118. PMID 32086167 DOI: 10.1016/J.Cbpa.2020.01.005 |
0.453 |
|
2020 |
Zwick CR, Renata H. Harnessing the biocatalytic potential of iron- and α-ketoglutarate-dependent dioxygenases in natural product total synthesis. Natural Product Reports. PMID 32055818 DOI: 10.1039/C9Np00075E |
0.409 |
|
2020 |
Li J, Li F, King-Smith E, Renata H. Merging chemoenzymatic and radical-based retrosynthetic logic for rapid and modular synthesis of oxidized meroterpenoids. Nature Chemistry. PMID 31959962 DOI: 10.1038/S41557-019-0407-6 |
0.761 |
|
2019 |
Zhang X, Renata H. Efficient Chemoenzymatic Synthesis of (2,3)-3-Hydroxy-3-Methylproline, a Key Fragment in Polyoxypeptin A and FR225659. Tetrahedron. 75: 3253-3257. PMID 31885405 DOI: 10.1016/J.Tet.2019.04.009 |
0.512 |
|
2019 |
Zwick CR, Sosa MB, Renata H. Characterization of a Citrulline 4-Hydroxylase from GE81112 Biosynthesis and Engineering of Its Substrate Specificity for the Chemoenzymatic Synthesis of Enduracididine. Angewandte Chemie (International Ed. in English). PMID 31610076 DOI: 10.1002/Anie.201910659 |
0.406 |
|
2019 |
Li J, Zhang X, Renata H. Asymmetric Chemoenzymatic Synthesis of (-)-Podophyllotoxin and Related Aryltetralin Lignans. Angewandte Chemie (International Ed. in English). PMID 31241812 DOI: 10.1002/Anie.201904102 |
0.528 |
|
2019 |
Dong LB, Zhang X, Shen B, Rudolf JD, Deng MR, Kalkreuter E, Cepeda AJ, Renata H. Cryptic and Stereospecific Hydroxylation, Oxidation, and Reduction in Platensimycin and Platencin Biosynthesis. Journal of the American Chemical Society. PMID 30735041 DOI: 10.1021/Jacs.8B13452 |
0.513 |
|
2018 |
Zhang RK, Chen K, Huang X, Wohlschlager L, Renata H, Arnold FH. Enzymatic assembly of carbon-carbon bonds via iron-catalysed sp C-H functionalization. Nature. PMID 30568304 DOI: 10.1038/S41586-018-0808-5 |
0.625 |
|
2018 |
Amatuni A, Renata H. Identification of a lysine 4-hydroxylase from the glidobactin biosynthesis and evaluation of its biocatalytic potential. Organic & Biomolecular Chemistry. PMID 30320324 DOI: 10.1039/C8Ob02054J |
0.37 |
|
2018 |
Li F, Zhang X, Renata H. Enzymatic CH functionalizations for natural product synthesis. Current Opinion in Chemical Biology. 49: 25-32. PMID 30269011 DOI: 10.1016/J.Cbpa.2018.09.004 |
0.743 |
|
2018 |
Rudolf JD, Dong LB, Zhang X, Renata H, Shen B. Cytochrome P450-Catalyzed Hydroxylation Initiating Ether Formation in Platensimycin Biosynthesis. Journal of the American Chemical Society. PMID 30216060 DOI: 10.1021/Jacs.8B08012 |
0.507 |
|
2018 |
Zwick CR, Renata H. Evolution of Biocatalytic and Chemocatalytic C-H Functionalization Strategy in the Synthesis of Manzacidin C. The Journal of Organic Chemistry. PMID 29771530 DOI: 10.1021/Acs.Joc.8B00248 |
0.43 |
|
2018 |
Zhang X, King-Smith E, Renata H. Efficient Total Synthesis of Tambromycin by Interfacing Chemocatalytic and Biocatalytic C-H Functionalization Logic. Angewandte Chemie (International Ed. in English). PMID 29481729 DOI: 10.1002/Anie.201801165 |
0.505 |
|
2018 |
Zwick CR, Renata H. A one-pot chemoenzymatic synthesis of (2S, 4R)-4-methylproline enables the first total synthesis of antiviral lipopeptide cavinafungin B Tetrahedron. 74: 6469-6473. DOI: 10.1016/J.Tet.2018.09.046 |
0.451 |
|
2017 |
Zwick CR, Renata H. Remote C-H Hydroxylation by an α-Ketoglutarate-Dependent Dioxygenase Enables Efficient Chemoenzymatic Synthesis of Manzacidin C and Proline Analogs. Journal of the American Chemical Society. PMID 29283572 DOI: 10.1021/Jacs.7B12918 |
0.494 |
|
2017 |
King-Smith E, Zwick CR, Renata H. Applications of Oxygenases in the Chemoenzymatic Total Synthesis of Complex Natural Products. Biochemistry. PMID 29140086 DOI: 10.1021/Acs.Biochem.7B00998 |
0.492 |
|
2017 |
Herwig L, Rice AJ, Bedbrook CN, Zhang RK, Lignell A, Cahn JK, Renata H, Dodani SC, Cho I, Cai L, Gradinaru V, Arnold FH. Directed Evolution of a Bright Near-Infrared Fluorescent Rhodopsin Using a Synthetic Chromophore. Cell Chemical Biology. PMID 28262559 DOI: 10.1016/J.Chembiol.2017.02.008 |
0.646 |
|
2016 |
Hernandez KE, Renata H, Lewis RD, Jennifer Kan SB, Zhang C, Forte J, Rozzell D, McIntosh JA, Arnold FH. Highly Stereoselective Biocatalytic Synthesis of Key Cyclopropane Intermediate to Ticagrelor. Acs Catalysis. 6: 7810-7813. PMID 28286694 DOI: 10.1021/Acscatal.6B02550 |
0.613 |
|
2016 |
Renata H, Lewis RD, Sweredoski MJ, Moradian A, Hess S, Wang ZJ, Arnold FH. Identification of Mechanism-Based Inactivation in P450-Catalyzed Cyclopropanation Facilitates Engineering of Improved Enzymes. Journal of the American Chemical Society. PMID 27573353 DOI: 10.1021/Jacs.6B06823 |
0.596 |
|
2015 |
Renata H, Wang ZJ, Arnold FH. Expanding the enzyme universe: accessing non-natural reactions by mechanism-guided directed evolution. Angewandte Chemie (International Ed. in English). 54: 3351-67. PMID 25649694 DOI: 10.1002/Anie.201409470 |
0.589 |
|
2015 |
Renata H, Zhou Q, Dünstl G, Felding J, Merchant RR, Yeh CH, Baran PS. Development of a concise synthesis of ouabagenin and hydroxylated corticosteroid analogues. Journal of the American Chemical Society. 137: 1330-40. PMID 25594682 DOI: 10.1021/Ja512022R |
0.754 |
|
2015 |
Renata H, Wang ZJ, Arnold FH. Ausdehnung des Enzym-Universums: Zugang zu nicht-natürlichen Reaktionen durch mechanismusgeleitete, gerichtete Evolution Angewandte Chemie. 127: 3408-3426. DOI: 10.1002/Ange.201409470 |
0.48 |
|
2014 |
Renata H, Wang ZJ, Kitto RZ, Arnold FH. P450-catalyzed asymmetric cyclopropanation of electron-deficient olefins under aerobic conditions. Catalysis Science & Technology. 4: 3640-3643. PMID 25221671 DOI: 10.1039/C4Cy00633J |
0.565 |
|
2014 |
Wang ZJ, Renata H, Peck NE, Farwell CC, Coelho PS, Arnold FH. Improved cyclopropanation activity of histidine-ligated cytochrome P450 enables the enantioselective formal synthesis of levomilnacipran. Angewandte Chemie (International Ed. in English). 53: 6810-3. PMID 24802161 DOI: 10.1002/Anie.201402809 |
0.76 |
|
2014 |
Wang ZJ, Peck NE, Renata H, Arnold FH. Cytochrome P450-Catalyzed Insertion of Carbenoids into N-H Bonds. Chemical Science (Royal Society of Chemistry : 2010). 5: 598-601. PMID 24490022 DOI: 10.1039/C3Sc52535J |
0.571 |
|
2014 |
Wang ZJ, Renata H, Peck NE, Farwell CC, Coelho PS, Arnold FH. Cover Picture: Improved Cyclopropanation Activity of Histidine-Ligated Cytochrome P450 Enables the Enantioselective Formal Synthesis of Levomilnacipran (Angew. Chem. Int. Ed. 26/2014) Angewandte Chemie International Edition. 53: 6571-6571. DOI: 10.1002/Anie.201404337 |
0.763 |
|
2014 |
Wang ZJ, Renata H, Peck NE, Farwell CC, Coelho PS, Arnold FH. Titelbild: Improved Cyclopropanation Activity of Histidine-Ligated Cytochrome P450 Enables the Enantioselective Formal Synthesis of Levomilnacipran (Angew. Chem. 26/2014) Angewandte Chemie. 126: 6689-6689. DOI: 10.1002/Ange.201404337 |
0.765 |
|
2013 |
Renata H, Zhou Q, Baran PS. Strategic redox relay enables a scalable synthesis of ouabagenin, a bioactive cardenolide. Science (New York, N.Y.). 339: 59-63. PMID 23288535 DOI: 10.1126/Science.1230631 |
0.724 |
|
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