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For: Thorpe TW, France SP, Hussain S, Marshall JR, Zawodny W, Mangas-sanchez J, Montgomery SL, Howard RM, Daniels DSB, Kumar R, Parmeggiani F, Turner NJ. One-Pot Biocatalytic Cascade Reduction of Cyclic Enimines for the Preparation of Diastereomerically Enriched N -Heterocycles. J Am Chem Soc 2019;141:19208-13. [DOI: 10.1021/jacs.9b10053] [Cited by in Crossref: 33] [Cited by in F6Publishing: 35] [Article Influence: 8.3] [Reference Citation Analysis]
Number Citing Articles
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2 Harawa V, Thorpe TW, Marshall JR, Sangster JJ, Gilio AK, Pirvu L, Heath RS, Angelastro A, Finnigan JD, Charnock SJ, Nafie JW, Grogan G, Whitehead RC, Turner NJ. Synthesis of Stereoenriched Piperidines via Chemo-Enzymatic Dearomatization of Activated Pyridines. J Am Chem Soc 2022. [DOI: 10.1021/jacs.2c07143] [Reference Citation Analysis]
3 Yang L, Li J, Xu Z, Yao P, Wu Q, Zhu D, Ma Y. Asymmetric Synthesis of Fused-Ring Tetrahydroisoquinolines and Tetrahydro-β-carbolines from 2-Arylethylamines via a Chemoenzymatic Approach. Org Lett 2022. [PMID: 36066397 DOI: 10.1021/acs.orglett.2c02466] [Reference Citation Analysis]
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10 Thorpe TW, Marshall JR, Harawa V, Ruscoe RE, Cuetos A, Finnigan JD, Angelastro A, Heath RS, Parmeggiani F, Charnock SJ, Howard RM, Kumar R, Daniels DSB, Grogan G, Turner NJ. Multifunctional biocatalyst for conjugate reduction and reductive amination. Nature 2022;604:86-91. [PMID: 35388195 DOI: 10.1038/s41586-022-04458-x] [Cited by in Crossref: 11] [Cited by in F6Publishing: 12] [Article Influence: 11.0] [Reference Citation Analysis]
11 Nicholls BT, Oblinsky DG, Kurtoic SI, Grosheva D, Ye Y, Scholes GD, Hyster TK. Engineering a Non‐Natural Photoenzyme for Improved Photon Efficiency**. Angewandte Chemie 2022;134. [DOI: 10.1002/ange.202113842] [Reference Citation Analysis]
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13 Gilio AK, Thorpe TW, Turner N, Grogan G. Reductive aminations by imine reductases: from milligrams to tons. Chem Sci . [DOI: 10.1039/d2sc00124a] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
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15 Nicholls BT, Oblinsky DG, Kurtoic SI, Grosheva D, Ye Y, Scholes GD, Hyster TK. Engineering a Non-Natural Photoenzyme for Improved Photon Efficiency*. Angew Chem Int Ed Engl 2021. [PMID: 34739168 DOI: 10.1002/anie.202113842] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 5.5] [Reference Citation Analysis]
16 Li M, Cui Y, Xu Z, Chen X, Feng J, Wang M, Yao P, Wu Q, Zhu D. Asymmetric Synthesis of N ‐Substituted γ‐Amino Esters and γ‐Lactams Containing α,γ‐Stereogenic Centers via a Stereoselective Enzymatic Cascade. Adv Synth Catal 2022;364:372-9. [DOI: 10.1002/adsc.202100953] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
17 Parmeggiani F, Brenna E, Colombo D, Gatti FG, Tentori F, Tessaro D. "A Study in Yellow": Investigations in the Stereoselectivity of Ene-Reductases. Chembiochem 2021. [PMID: 34586700 DOI: 10.1002/cbic.202100445] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
18 Chatterjee A, Rao DHS, Kumar Padhi S. One‐Pot Enzyme Cascade Catalyzed Asymmetrization of Primary Alcohols: Synthesis of Enantiocomplementary Chiral β‐Nitroalcohols. Adv Synth Catal 2021;363:5310-8. [DOI: 10.1002/adsc.202100803] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
19 Shi Q, Jia Y, Wang H, Li S, Li H, Guo J, Dou T, Qin B, You S. Identification of four ene reductases and their preliminary exploration in the asymmetric synthesis of (R)-dihydrocarvone and (R)-profen derivatives. Enzyme Microb Technol 2021;150:109880. [PMID: 34489033 DOI: 10.1016/j.enzmictec.2021.109880] [Reference Citation Analysis]
20 Feng J, Geng WC, Jiang H, Wu B. Recent advances in biocatalysis of nitrogen-containing heterocycles. Biotechnol Adv 2022;54:107813. [PMID: 34450199 DOI: 10.1016/j.biotechadv.2021.107813] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
21 Cigan E, Eggbauer B, Schrittwieser JH, Kroutil W. The role of biocatalysis in the asymmetric synthesis of alkaloids - an update. RSC Adv 2021;11:28223-70. [PMID: 35480754 DOI: 10.1039/d1ra04181a] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 3.0] [Reference Citation Analysis]
22 Hall M. Enzymatic strategies for asymmetric synthesis. RSC Chem Biol 2021;2:958-89. [PMID: 34458820 DOI: 10.1039/d1cb00080b] [Cited by in Crossref: 15] [Cited by in F6Publishing: 17] [Article Influence: 7.5] [Reference Citation Analysis]
23 Liu G, Li S, Shi Q, Li H, Guo J, Ouyang J, Jia X, Zhang L, You S, Qin B. Engineering of Saccharomyces pastorianus old yellow enzyme 1 for the synthesis of pharmacologically active (S)-profen derivatives. Molecular Catalysis 2021;507:111568. [DOI: 10.1016/j.mcat.2021.111568] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
24 Albarrán‐velo J, González‐granda S, López‐agudo M, Gotor‐fernández V. Practical Multienzymatic Transformations: Combining Enzymes for the One‐pot Synthesis of Organic Molecules in a Straightforward Manner. Biocatalysis for Practitioners 2021. [DOI: 10.1002/9783527824465.ch13] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
25 Kempa EE, Galman JL, Parmeggiani F, Marshall JR, Malassis J, Fontenelle CQ, Vendeville JB, Linclau B, Charnock SJ, Flitsch SL, Turner NJ, Barran PE. Rapid Screening of Diverse Biotransformations for Enzyme Evolution. JACS Au 2021;1:508-16. [PMID: 34056634 DOI: 10.1021/jacsau.1c00027] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
26 Cosgrove SC, Ramsden JI, Mangas‐sanchez J, Turner NJ. Biocatalytic Synthesis of Chiral Amines Using Oxidoreductases. In: Ricci A, Bernardi L, editors. Methodologies in Amine Synthesis. Wiley; 2021. pp. 243-83. [DOI: 10.1002/9783527826186.ch7] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
27 Finnigan W, Hepworth LJ, Flitsch SL, Turner NJ. RetroBioCat as a computer-aided synthesis planning tool for biocatalytic reactions and cascades. Nat Catal 2021;4:98-104. [PMID: 33604511 DOI: 10.1038/s41929-020-00556-z] [Cited by in Crossref: 58] [Cited by in F6Publishing: 59] [Article Influence: 29.0] [Reference Citation Analysis]
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29 Xiao X, Shao B, Lu Y, Cao Q, Xia C, Chen F. Recent Advances in Asymmetric Organomulticatalysis. Adv Synth Catal 2021;363:352-87. [DOI: 10.1002/adsc.202000961] [Cited by in Crossref: 26] [Cited by in F6Publishing: 28] [Article Influence: 8.7] [Reference Citation Analysis]
30 Kuska J, O'Reilly E. Engineered biosynthetic pathways and biocatalytic cascades for sustainable synthesis. Curr Opin Chem Biol 2020;58:146-54. [PMID: 33152607 DOI: 10.1016/j.cbpa.2020.08.006] [Cited by in Crossref: 12] [Cited by in F6Publishing: 11] [Article Influence: 4.0] [Reference Citation Analysis]
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33 Feng J, Li R, Zhang S, Bu Y, Chen Y, Cui Y, Lin B, Chen Y, Tao Y, Wu B. Bioretrosynthesis of Functionalized N-Heterocycles from Glucose via One-Pot Tandem Collaborations of Designed Microbes. Adv Sci (Weinh) 2020;7:2001188. [PMID: 32995125 DOI: 10.1002/advs.202001188] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 2.0] [Reference Citation Analysis]
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