!!Todd B. Marder - Selected Publications
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Publications: 443; Patents: 7 applied (2 granted thus far); Web of Science 10.04.2024: h-Index 101; Citations: 33,858 (non-self-citations 30,100), 105 papers with 100 or more citations each, 139 papers with 75 or more citations, 189 papers with 50 or more citations each. Google Scholar: h-Index 103; 36,384 citations.\\
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1. J. Hu, M. Tang, J. Wang, Z. Wu, A. Friedrich, T.B. Marder*, "Photocatalyzed Borylcyclopropanation of Alkenes with a (Diborylmethyl)iodide Reagent", Angew. Chem. Int. Ed., 2023, 62, e202305175, DOI: 10.1002/anie.202305175 (Designated as a Hot Paper).\\
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2. X. Zhang, F. Rauch, J. Niedens, R. da Silva, A. Friedrich, A. Nowak-Króll, S. Garden, T.B. Marder*, "Electrophilic C–H Borylation of Aza[[5]]helicenes Leading to Bowl-Shaped Quasi-[[7]Circulenes with Switchable Dynamics", J. Am. Chem. Soc., 2022, 144, 22316-22324, DOI: 10.1021/jacs.2c10865. \\
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Highlighted in ChemistryViews: https://www.chemistryviews.org/quasi-7circulenes-prepared-from-aza5helicenes/ \\
Highlighted by D. Zhao and X. Bai, Synfacts, 2023, 19, 0243, DOI: 10.1055/s-0042-1753326\\
[https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0042-1753326].\\
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3. Z. Wu, J. C. Roldao, F. Rauch, A. Friedrich, M. Ferger, F. Würthner, J. Gierschner, T.B. Marder*, "Pure Boric Acid Does Not Show Room Temperature Phosphorescence (RTP)", Angew. Chem. Int. Ed., 2022, 61, e202200599, DOI: 10.1002/anie.202200599 (Designated as a Hot Paper). \\
Highlighted in Nachrichten aus der Chemie, April 2022, vol. 70, p. 55.\\
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4. J. He, F. Rauch, A. Friedrich, J. Krebs, I. Krummenacher, R. Bertermann, J. Nitsch, H. Braunschweig, M. Finze, T.B. Marder*, "Phenylpyridyl-fused Boroles: A Unique Coordination Mode and Weak B–N Coordination-Induced Dual Fluorescence", Angew. Chem. Int. Ed., 2021, 60, 4833-4840, DOI: 10.1002/anie.202013692 (Designated as a Hot Paper).\\
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5. A. Friedrich, I.E. Collings, K.F. Dziubek, S. Fanetti, K. Radacki, J. Ruiz-Fuertes, J. Pellicer-Porres, M. Hanfland, D. Sieh, R. Bini, S.J. Clark, T.B. Marder*, "Pressure-Induced Polymerization of Polycyclic Arene-Perfluoroarene Cocrystals: Single Crystal X-ray Diffraction Studies, Reaction Kinetics, and Design of Columnar Hydrofluorocarbons", J. Am. Chem. Soc., 2020, 142, 18907-18923, DOI: 10.1021/jacs.0c09021. \\
JACS Spotlight: J. Am. Chem. Soc., 2020, 142, 18733-18734, DOI: 10.1021/jacs.0c11191.\\
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6. Y.M. Tian, X.N. Guo, I. Krummenacher, Z. Wu, J. Nitsch, H. Braunschweig, U. Radius, T.B. Marder*, "Visible-Light-Induced Ni-Catalyzed Radical Borylation of Chloroarenes", J. Am. Chem. Soc., 2020, 142, 18231-18242, DOI: 10.1021/jacs.0c08834.\\
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7. Y.-M. Tian, X.-N. Guo, Z. Wu, A. Friedrich, S.A. Westcott, H. Braunschweig, U. Radius, T.B. Marder*, "Ni-Catalyzed Traceless, Directed C3-Selective C-H Borylation of Indoles", J. Am. Chem. Soc., 2020, 142, 13136-13144, DOI: 10.1021/jacs.0c05434.\\
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Highlighted in Org. Process Res. Dev., 2020, 24, 1549-1557, DOI: 10.1021/acs.oprd.0c003181.\\
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8. Z. Wu, J. Nitsch, J. Schuster, A. Friedrich, K. Edkins, M. Loebnitz, F. Dinkelbach, V. Stepanenko, F. Würthner, C.M. Marian, L. Ji, T.B. Marder*, "Persistent Room Temperature Phosphorescence from Triarylboranes", Angew. Chem. Int. Ed., 2020, 59, 17137-17144, DOI: 10.1002/anie.202007610 (Designated as a Very Important Paper).\\
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9. Y.P. Budiman, A. Jayaraman, A. Friedrich, F. Kerner, U. Radius, T.B. Marder*, "Palladium-Catalyzed Homocoupling of Highly Fluorinated Arylboronates: Studies of the Influence of Strongly vs. Weakly Coordinating Solvents on the Reductive Elimination Process", J. Am. Chem. Soc., 2020, 142, 6036-6050, DOI: 10.1021/jacs.9b11871.\\
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10. X. Liu, W. Ming, A. Friedrich, F. Kerner, T.B. Marder*, "Copper-Catalyzed Triboration of Terminal Alkynes Using B2pin2: Efficient Synthesis of 1,1,2-Triborylalkenes", Angew. Chem. Int. Ed., 2020, 59, 304-309, DOI: 10.1002/anie.201908466.\\
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__For recent reviews, see:__\\
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1. C.B. Kelly, L. Thai-Savard, J. Hu, T.B. Marder, G.A. Molander, and A.B. Charette, “Modern Cyclopropanation via Non-Traditional Building Blocks,” ChemCatChem, 2024, e202400110. DOI: 10.1002/cctc.202400110. Invited Concepts Article\\
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2. Y.P. Budiman, R.N. Perutz, P.G: Steel, U. Radius, and T.B. Marder, “Applications of Transition Metal-Catalyzed ortho-Fluorine-Directed C-H Functionalization of (Poly)fluoroarenes in Organic Synthesis,” Chem. Rev., 2024, 124, xxxx. (accepted February 2024). DOI: 10.1021/acs.chemrev.3c00793.\\
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3. S.M. Berger and T.B. Marder, “Applications of Triarylborane Materials in Cell Imaging and Sensing of Bio-relevant Molecules such as DNA, RNA, and Proteins,” Invited review for special thematic issue for Seth Marder’s 60th birthday, Mater. Horiz., 2022, 9, 112-120. DOI: 10.1039/D1MH00696G.\\
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4. J. Hu, M. Ferger, Z. Shi, and T.B. Marder, “Recent Advances in Asymmetric Borylation by Transition Metal Catalysis,” Chem. Soc. Rev., 2021, 50, 13129-13188. DOI: 10.1039/d0cs00843e.\\
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5. S.K. Bose, L. Mao, L. Kuehn, U. Radius, J. Nekvinda, W. Santos, S.A. Westcott, P.G. Steel, and T.B. Marder, “First-Row d-Block Element-Catalyzed Carbon-Boron Bond Formation and Related Processes,” Chem. Rev., 2021, 121, 13238-13341. DOI: 10.1021/acs.chemrev.1c00255\\
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6. W. Ming, H. Soor, X. Liu, A. Trofimova, A. Yudin, and T.B. Marder, “alpha-Aminoboronates: Recent Advances in their Preparation and Synthetic Applications,” Chem. Soc. Rev.,2021, 50, 12151-12188. DOI: 10.1039/d1cs00423a.\\
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7. Z. Wu, J. Nitsch, and T.B. Marder, “Persistent Room-Temperature Phosphorescence from Purely Organic Molecules and Multi-Component Systems,” Invited review, Adv. Opt. Mater., 2021, 9, 2100411. DOI: 10.1002/adom.202100411.\\
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8. J. Maier and T.B. Marder, "Mechanistic and Kinetic Factors of ortho-Benzyne Formation in Hexadehydro-Diels-Alder (HDDA) Reactions" Chem. Eur. J., 2021, 27, 7978-7991. DOI: 10.1002/chem.202100608. (Mini review) (Selected by the Editorial Office for their Showcase of outstanding Review-type articles)\\
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9. Y.-M. Tian, X.-N. Guo, H. Braunschweig, U. Radius, and T.B. Marder, “Photoinduced Borylation for the Synthesis of Organoboron Compounds,” Chem. Rev. 2021, 121, 3561-3597. DOI: 10.1021/acs.chemrev.0c01236.\\
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10. S.M. Berger, M. Ferger, and T.B. Marder, "Synthetic Approaches to Triarylboranes from 1885 to 2020,” Chem. Eur. J., 2021, 27, 7043-7058. DOI: 10.1002/chem.202005302. (Selected by the Editorial Office for their Showcase of outstanding Review-type articles)\\
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11. Y.P. Budiman, S.A. Westcott, U. Radius, and T.B. Marder, “Fluorinated Aryl Boronates as Building Blocks in Organic Synthesis,” Adv. Synth. Catal., 2021, 363, 2224-2255. DOI: 10.1002/adsc.202001291. Invited review for special thematic issue on Boron in Catalysis and Organic Synthesis (E. Fernandez, Guest Editor). (Designated as a Very Important Paper).\\
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12. J. He, F. Rauch, M. Finze, and T.B. Marder, “(Hetero)Arene-Fused Boroles: A Broad Spectrum of Applications,” Chem. Sci., 2021, 12 128-147. DOI: 10.1039/d0sc05676f.\\
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13. O. Diamond and T.B. Marder, “Methodology and Applications of the Hexadehydro-Diels-Alder (HDDA) Reaction,” Invited Review for special issue on “Novel pi-Electron Molecular Scaffolds,” Org. Chem. Frontiers, 2017, 4, 891-910. DOI: 10.1039/C7QO00071E.\\
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14. F.K. Scharnagl, S.K. Bose, and T.B. Marder, “Acylboranes: Synthetic Strategies and Applications,” Invited Review, Org. Biomol. Chem., 2017, 15, 1738-1752. DOI: 10.1039/C6OB02425D.\\
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15. L. Ji, S. Griesbeck, and T.B. Marder, “Recent Developments in and Perspectives on Three-Coordinate Boron Materials: A Bright Future,” Invited Review, Chem. Sci., 2017, 8, 846-863. DOI: 10.1039/C6SC04245G.\\
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16. E.C. Neeve, S.J. Geier, I.A.I. Mkhalid, S.A. Westcott, and T.B. Marder, “Diboron(4) Compounds: From Structural Curiosity to Synthetic Workhorse,” Chem. Rev., 2016, 116, 9091-9161. DOI: 10.1021/acs.chemrev.6b00193.\\
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17. S. Würtemberger-Pietsch, U. Radius, and T.B. Marder, “25 Years of N-Heterocyclic Carbenes: Activation of Both Main-Group Element-Element Bonds and NHCs Themselves,” Invited Dalton Perspective, Dalton Trans., 2016, 45, 5880-5895. DOI: 10.1039/C5DT04106F.\\
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18. R.D. Dewhurst, E.C. Neeve, H. Braunschweig, and T.B. Marder, “sp2-sp3 Diboranes: Astounding Structural Variability and Mild Sources of Nucleophilic Boron for Organic Synthesis,” Chem. Commun., 2015, 51, 9594-9607. (Feature Article). DOI: 10.1039/c5cc02316e.\\ \\[{ALLOW view All}][{ALLOW edit tmarder}][{ALLOW upload tmarder}][{ALLOW comment All}]