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Abigail Doyle - Publications

Affiliations: 
2008-2021 Chemistry Princeton University, Princeton, NJ 
 2021- University of California, Los Angeles, Los Angeles, CA 
Area:
organic and organometallic catalysis
Website:
https://doyle.chem.ucla.edu/
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61 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2024 Sheng H, Sun J, Rodríguez O, Hoar BB, Zhang W, Xiang D, Tang T, Hazra A, Min DS, Doyle AG, Sigman MS, Costentin C, Gu Q, Rodríguez-López J, Liu C. Autonomous closed-loop mechanistic investigation of molecular electrochemistry via automation. Nature Communications. 15: 2781. PMID 38555303 DOI: 10.1038/s41467-024-47210-x  0.491
2023 Raghavan P, Haas BC, Ruos ME, Schleinitz J, Doyle AG, Reisman SE, Sigman MS, Coley CW. Dataset Design for Building Models of Chemical Reactivity. Acs Central Science. 9: 2196-2204. PMID 38161380 DOI: 10.1021/acscentsci.3c01163  0.658
2023 Borowski JE, Newman-Stonebraker SH, Doyle AG. Comparison of Monophosphine and Bisphosphine Precatalysts for Ni-Catalyzed Suzuki-Miyaura Cross-Coupling: Understanding the Role of the Ligation State in Catalysis. Acs Catalysis. 13: 7966-7977. PMID 38037565 DOI: 10.1021/acscatal.3c01331  0.78
2023 Williams WL, Gutiérrez-Valencia NE, Doyle AG. Branched-Selective Cross-Electrophile Coupling of 2-Alkyl Aziridines and (Hetero)aryl Iodides Using Ti/Ni Catalysis. Journal of the American Chemical Society. 145: 24175-24183. PMID 37888947 DOI: 10.1021/jacs.3c08301  0.409
2023 Newman-Stonebraker SH, Raab TJ, Roshandel H, Doyle AG. Synthesis of Nickel(I)-Bromide Complexes via Oxidation and Ligand Displacement: Evaluation of Ligand Effects on Speciation and Reactivity. Journal of the American Chemical Society. PMID 37610310 DOI: 10.1021/jacs.3c06233  0.767
2023 Dunlap JH, Ethier JG, Putnam-Neeb AA, Iyer S, Luo SL, Feng H, Garrido Torres JA, Doyle AG, Swager TM, Vaia RA, Mirau P, Crouse CA, Baldwin LA. Continuous flow synthesis of pyridinium salts accelerated by multi-objective Bayesian optimization with active learning. Chemical Science. 14: 8061-8069. PMID 37538827 DOI: 10.1039/d3sc01303k  0.344
2023 Saebi M, Nan B, Herr JE, Wahlers J, Guo Z, Zurański AM, Kogej T, Norrby PO, Doyle AG, Chawla NV, Wiest O. On the use of real-world datasets for reaction yield prediction. Chemical Science. 14: 4997-5005. PMID 37206399 DOI: 10.1039/d2sc06041h  0.494
2023 Tang T, Hazra A, Min DS, Williams WL, Jones E, Doyle AG, Sigman MS. Interrogating the Mechanistic Features of Ni(I)-Mediated Aryl Iodide Oxidative Addition Using Electroanalytical and Statistical Modeling Techniques. Journal of the American Chemical Society. PMID 37014945 DOI: 10.1021/jacs.3c01726  0.537
2022 Murray PRD, Leibler IN, Hell SM, Villalona E, Doyle AG, Knowles RR. Radical Redox Annulations: A General Light-Driven Method for the Synthesis of Saturated Heterocycles. Acs Catalysis. 12: 13732-13740. PMID 36366762 DOI: 10.1021/acscatal.2c04316  0.641
2022 Dongbang S, Doyle AG. Ni/Photoredox-Catalyzed C(sp)-C(sp) Coupling between Aziridines and Acetals as Alcohol-Derived Alkyl Radical Precursors. Journal of the American Chemical Society. 144: 20067-20077. PMID 36256882 DOI: 10.1021/jacs.2c09294  0.321
2022 Newman-Stonebraker SH, Wang JY, Jeffrey PD, Doyle AG. Structure-Reactivity Relationships of Buchwald-Type Phosphines in Nickel-Catalyzed Cross-Couplings. Journal of the American Chemical Society. PMID 36250758 DOI: 10.1021/jacs.2c09840  0.778
2022 Ting SI, Williams WL, Doyle AG. Oxidative Addition of Aryl Halides to a Ni(I)-Bipyridine Complex. Journal of the American Chemical Society. 144: 5575-5582. PMID 35298885 DOI: 10.1021/jacs.2c00462  0.303
2022 Kariofillis SK, Jiang S, Żurański AM, Gandhi SS, Martinez Alvarado JI, Doyle AG. Using Data Science To Guide Aryl Bromide Substrate Scope Analysis in a Ni/Photoredox-Catalyzed Cross-Coupling with Acetals as Alcohol-Derived Radical Sources. Journal of the American Chemical Society. PMID 34985904 DOI: 10.1021/jacs.1c12203  0.372
2021 Williams WL, Zeng L, Gensch T, Sigman MS, Doyle AG, Anslyn EV. The Evolution of Data-Driven Modeling in Organic Chemistry. Acs Central Science. 7: 1622-1637. PMID 34729406 DOI: 10.1021/acscentsci.1c00535  0.52
2021 Newman-Stonebraker SH, Smith SR, Borowski JE, Peters E, Gensch T, Johnson HC, Sigman MS, Doyle AG. Univariate classification of phosphine ligation state and reactivity in cross-coupling catalysis. Science (New York, N.Y.). 374: 301-308. PMID 34648340 DOI: 10.1126/science.abj4213  0.74
2021 Lau SH, Borden MA, Steiman TJ, Wang LS, Parasram M, Doyle AG. Ni/Photoredox-Catalyzed Enantioselective Cross-Electrophile Coupling of Styrene Oxides with Aryl Iodides. Journal of the American Chemical Society. PMID 34542286 DOI: 10.1021/jacs.1c08105  0.427
2021 Kariofillis SK, Doyle AG. Synthetic and Mechanistic Implications of Chlorine Photoelimination in Nickel/Photoredox C(sp)-H Cross-Coupling. Accounts of Chemical Research. PMID 33511841 DOI: 10.1021/acs.accounts.0c00694  0.433
2020 Parasram M, Shields BJ, Ahmad O, Knauber T, Doyle AG. Regioselective Cross-Electrophile Coupling of Epoxides and (Hetero)aryl Iodides via Ni/Ti/Photoredox Catalysis. Acs Catalysis. 10: 5821-5827. PMID 32747870 DOI: 10.1021/acscatal.0c01199  0.453
2020 Webb EW, Park JB, Cole EL, Donnelly DJ, Bonacorsi SJ, Ewing WR, Doyle AG. Nucleophilic (Radio)Fluorination of Redox-Active Esters via Radical-Polar Crossover Enabled by Photoredox Catalysis. Journal of the American Chemical Society. PMID 32378889 DOI: 10.1021/jacs.0c03125  0.342
2020 Estrada JG, Williams WL, Ting SI, Doyle AG. Role of Electron-Deficient Olefin Ligands in a Ni-Catalyzed Aziridine Cross-Coupling To Generate Quaternary Carbons. Journal of the American Chemical Society. PMID 32348673 DOI: 10.1021/jacs.0c02237  0.402
2020 Steiman TJ, Liu J, Mengiste A, Doyle AG. Synthesis of β-Phenethylamines via Ni/Photoredox Cross-Electrophile Coupling of Aliphatic Aziridines and Aryl Iodides. Journal of the American Chemical Society. PMID 32250602 DOI: 10.1021/jacs.0c01724  0.391
2020 Parasram M, Shields BJ, Ahmad O, Knauber T, Doyle AG. Regioselective Cross-Electrophile Coupling of Epoxides and (Hetero)aryl Iodides via Ni/Ti/Photoredox Catalysis Acs Catalysis. 10: 5821-5827. DOI: 10.1021/acscatal.0c01199  0.355
2019 Martinez Alvarado JI, Ertel AB, Stegner A, Stache EE, Doyle AG. Direct Use of Carboxylic Acids in the Photocatalytic Hydroacylation of Styrenes To Generate Dialkyl Ketones. Organic Letters. PMID 31750667 DOI: 10.1021/acs.orglett.9b03871  0.766
2019 Aspuru-Guzik A, Baik MH, Balasubramanian S, Banerjee R, Bart S, Borduas-Dedekind N, Chang S, Chen P, Corminboeuf C, Coudert FX, Cronin L, Crudden C, Cuk T, Doyle AG, Fan C, et al. Charting a course for chemistry. Nature Chemistry. 11: 286-294. PMID 30903035 DOI: 10.1038/S41557-019-0236-7  0.667
2018 Stache EE, Ertel AB, Tomislav R, Doyle AG. Generation of Phosphoranyl Radicals via Photoredox Catalysis Enables Voltage-Independent Activation of Strong C-O Bonds. Acs Catalysis. 8: 11134-11139. PMID 31367474 DOI: 10.1021/Acscatal.8B03592  0.746
2018 Woods BP, Orlandi M, Huang CD, Sigman MS, Doyle AG. Correction to "Nickel-Catalyzed Enantioselective Reductive Cross-Coupling of Styrenyl Aziridines". Journal of the American Chemical Society. PMID 29889505 DOI: 10.1021/Jacs.8B05650  0.577
2018 Shields BJ, Kudisch B, Scholes GD, Doyle AG. Long-Lived Charge Transfer States of Nickel(II) Aryl Halide Complexes Facilitate Bimolecular Photoinduced Electron Transfer. Journal of the American Chemical Society. PMID 29400956 DOI: 10.1021/Jacs.7B13281  0.338
2018 Heinz C, Lutz JP, Simmons EM, Miller MM, Ewing WR, Doyle AG. A Ni-Catalyzed Carbon-Carbon Bond-Forming Reductive Amination. Journal of the American Chemical Society. PMID 29341599 DOI: 10.1021/Jacs.7B12212  0.417
2017 Wu K, Doyle AG. Parameterization of phosphine ligands demonstrates enhancement of nickel catalysis via remote steric effects. Nature Chemistry. 9: 779-784. PMID 28754948 DOI: 10.1038/Nchem.2741  0.36
2017 Woods BP, Orlandi M, Huang CY, Sigman MS, Doyle AG. Nickel-Catalyzed Enantioselective Reductive Cross-Coupling of Styrenyl Aziridines. Journal of the American Chemical Society. PMID 28406622 DOI: 10.1021/Jacs.7B03448  0.629
2017 Stache EE, Rovis T, Doyle AG. Dual Nickel- and Photoredox-Catalyzed Enantioselective Desymmetrization of Cyclic meso-Anhydrides. Angewandte Chemie (International Ed. in English). PMID 28230304 DOI: 10.1002/Anie.201700097  0.799
2016 Lutz JP, Chau ST, Doyle AG. Nickel-catalyzed enantioselective arylation of pyridine. Chemical Science. 7: 4105-4109. PMID 28058106 DOI: 10.1039/c6sc00702c  0.438
2016 Ahneman DT, Doyle AG. C-H functionalization of amines with aryl halides by nickel-photoredox catalysis. Chemical Science. 7: 7002-7006. PMID 28058105 DOI: 10.1039/C6SC02815B  0.326
2016 Gray EE, Nielsen MK, Choquette KA, Kalow JA, Graham TJ, Doyle AG. Nucleophilic (Radio)Fluorination of α-Diazocarbonyl Compounds Enabled by Copper-Catalyzed H-F Insertion. Journal of the American Chemical Society. PMID 27500313 DOI: 10.1021/Jacs.6B06770  0.614
2016 Lutz JP, Chau ST, Doyle AG. Nickel-catalyzed enantioselective arylation of pyridine Chemical Science. 7: 4105-4109. DOI: 10.1039/c6sc00702c  0.42
2015 Arendt KM, Doyle AG. Dialkyl Ether Formation by Nickel-Catalyzed Cross-Coupling of Acetals and Aryl Iodides. Angewandte Chemie (International Ed. in English). 54: 9876-80. PMID 26219537 DOI: 10.1002/anie.201503936  0.445
2015 Huang CY, Doyle AG. Electron-deficient olefin ligands enable generation of quaternary carbons by Ni-catalyzed cross-coupling. Journal of the American Chemical Society. 137: 5638-41. PMID 25879801 DOI: 10.1021/jacs.5b02503  0.35
2014 Zuo Z, Ahneman DT, Chu L, Terrett JA, Doyle AG, MacMillan DW. Dual catalysis. Merging photoredox with nickel catalysis: coupling of α-carboxyl sp³-carbons with aryl halides. Science (New York, N.Y.). 345: 437-40. PMID 24903563 DOI: 10.1126/Science.1255525  0.32
2014 Shields JD, Ahneman DT, Graham TJ, Doyle AG. Enantioselective, nickel-catalyzed Suzuki cross-coupling of quinolinium ions. Organic Letters. 16: 142-5. PMID 24279380 DOI: 10.1021/ol4031364  0.318
2014 Katcher MH, Norrby PO, Doyle AG. Mechanistic investigations of palladium-catalyzed allylic fluorination Organometallics. 33: 2121-2133. DOI: 10.1021/Om401240P  0.782
2013 Nielsen DK, Huang CY, Doyle AG. Directed nickel-catalyzed negishi cross coupling of alkyl aziridines. Journal of the American Chemical Society. 135: 13605-9. PMID 23961769 DOI: 10.1021/ja4076716  0.627
2013 Braun MG, Doyle AG. Palladium-catalyzed allylic C-H fluorination. Journal of the American Chemical Society. 135: 12990-3. PMID 23947740 DOI: 10.1021/Ja407223G  0.598
2013 Chau ST, Lutz JP, Wu K, Doyle AG. Nickel-catalyzed enantioselective arylation of pyridinium ions: harnessing an iminium ion activation mode. Angewandte Chemie (International Ed. in English). 52: 9153-6. PMID 23843307 DOI: 10.1002/Anie.201303994  0.442
2013 Braun MG, Katcher MH, Doyle AG. Carbofluorination via a palladium-catalyzed cascade reaction Chemical Science. 4: 1216-1220. DOI: 10.1039/C2Sc22198E  0.8
2013 Kalow JA, Doyle AG. Enantioselective fluoride ring opening of aziridines enabled by cooperative Lewis acid catalysis Tetrahedron. 69: 5702-5709. DOI: 10.1016/J.Tet.2013.01.062  0.692
2012 Sylvester KT, Wu K, Doyle AG. Mechanistic investigation of the nickel-catalyzed Suzuki reaction of N,O-acetals: evidence for boronic acid assisted oxidative addition and an iminium activation pathway. Journal of the American Chemical Society. 134: 16967-70. PMID 23030789 DOI: 10.1021/ja3079362  0.553
2012 Kalow JA, Schmitt DE, Doyle AG. Synthesis of β-fluoroamines by Lewis base catalyzed hydrofluorination of aziridines. The Journal of Organic Chemistry. 77: 4177-83. PMID 22489747 DOI: 10.1021/Jo300433A  0.67
2012 Huang CY, Doyle AG. Nickel-catalyzed Negishi alkylations of styrenyl aziridines. Journal of the American Chemical Society. 134: 9541-4. PMID 22414150 DOI: 10.1021/ja3013825  0.432
2012 Graham TJ, Doyle AG. Nickel-catalyzed cross-coupling of chromene acetals and boronic acids. Organic Letters. 14: 1616-9. PMID 22385385 DOI: 10.1021/ol300364s  0.318
2012 Shaw TW, Kalow JA, Doyle AG. Fluoride ring-opening kinetic resolution of terminal epoxides: Preparation of (s)-2-fluoro-1-phenylethanol Organic Syntheses. 89: 9-18. DOI: 10.15227/Orgsyn.089.0009  0.619
2011 Katcher MH, Sha A, Doyle AG. Palladium-catalyzed regio- and enantioselective fluorination of acyclic allylic halides. Journal of the American Chemical Society. 133: 15902-5. PMID 21894884 DOI: 10.1021/Ja206960K  0.8
2011 Kalow JA, Doyle AG. Mechanistic investigations of cooperative catalysis in the enantioselective fluorination of epoxides. Journal of the American Chemical Society. 133: 16001-12. PMID 21863842 DOI: 10.1021/Ja207256S  0.701
2011 Nielsen DK, Doyle AG. Nickel-catalyzed cross-coupling of styrenyl epoxides with boronic acids. Angewandte Chemie (International Ed. in English). 50: 6056-9. PMID 21574227 DOI: 10.1002/anie.201101191  0.568
2010 Katcher MH, Doyle AG. Palladium-catalyzed asymmetric synthesis of allylic fluorides. Journal of the American Chemical Society. 132: 17402-4. PMID 21087003 DOI: 10.1021/Ja109120N  0.792
2010 Kalow JA, Doyle AG. Enantioselective ring opening of epoxides by fluoride anion promoted by a cooperative dual-catalyst system. Journal of the American Chemical Society. 132: 3268-9. PMID 20163118 DOI: 10.1021/Ja100161D  0.701
2008 Reisman SE, Doyle AG, Jacobsen EN. Enantioselective thiourea-catalyzed additions to oxocarbenium ions. Journal of the American Chemical Society. 130: 7198-9. PMID 18479086 DOI: 10.1021/Ja801514M  0.705
2007 Doyle AG, Jacobsen EN. Small-molecule H-bond donors in asymmetric catalysis. Chemical Reviews. 107: 5713-43. PMID 18072808 DOI: 10.1021/Cr068373R  0.404
2007 Doyle AG, Jacobsen EN. Enantioselective alkylation of acyclic alpha,alpha-disubstituted tributyltin enolates catalyzed by a {Cr(salen)} complex. Angewandte Chemie (International Ed. in English). 46: 3701-5. PMID 17407117 DOI: 10.1002/Anie.200604901  0.421
2007 Jacobsen E, Doyle A. Asymmetric α-Alkylation of Acyclic Tin Enolates Synfacts. 2007: 0732-0732. DOI: 10.1055/s-2007-968614  0.434
2005 Doyle AG, Jacobsen EN. Enantioselective alkylations of tributyltin enolates catalyzed by Cr(salen)Cl: access to enantiomerically enriched all-carbon quaternary centers. Journal of the American Chemical Society. 127: 62-3. PMID 15631449 DOI: 10.1021/Ja043601P  0.541
2001 White MC, Doyle AG, Jacobsen EN. A synthetically useful, self-assembling MMO mimic system for catalytic alkene epoxidation with aqueous H2O2. Journal of the American Chemical Society. 123: 7194-5. PMID 11459514 DOI: 10.1021/Ja015884G  0.663
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