Publications
2024
-Polymer-Supported Strong Lewis Acid Phosphonium Cation Catalysis Applied to Sydnone Synthesis. Dol, R. Kovljenic, N.; Dudding, T. Chem. Commun. 2024, ASAP. (https://doi.org/10.1039/D4CC03412K)
- Complementary Tandem Reaction Manifolds and "Switch Mechanisms" in the Reaction of Epoxides with Selectfluor. Garrison, N. G.; Holt, E.; Wang, M.; Rowshanpour, R.; Kiame, N.; Lam, W.; Borukhova, F.; Dudding, T.; Lectka, T. J. Org. Chem. 2024, ASAP. (doi.org/10.1021/acs.joc.4c01470)
- A Rigidified Macrocyclic Grubbs Complex: A Rare Example of In- and Out-Isomers that Show a Dramatic Difference in Catalytic Reactivity. Davalos-Moringo, A. R.; Vemulapalli, S.; Dudding, T.; Diver, S. T. Organometallics 2024, ASAP. (doi.org/10.1021/acs.organomet.4c00331)
- Streamlining Fluoroalkenyl Arene Synthesis Illuminated with Mechanistic Insights. Rajabalinia, S.; Hoford, S.; Dudding, T. ACS Omega 2024, 9, 21152-21163. (https://doi.org/10.1021/acsomega.4c01055)
- Catalytic Light-Driven Strategy for Transforming Oximes to Carbonyls. White, B.; Dudding, T. J. Org. Chem. 2024, 89, 4569-4578. (https://doi.org/10.1021/acs.joc.3c02793)
-A Boron Scan of Ethyl Acetoacetate Leads to Versatile Building Blocks. Trofimova, A.; White, B.; Diaz, D. B.; Sirvinskas, M. J.; Lough, A.; Dudding, T.; Yudin, A. K. Angew. Chem. Int. Ed. 2024, e202319842. (https://doi.org/10.1002/anie.202319842)
-The Role of Attractive Non-Covalent Interactions in Peptide Macrocyclization. Diaz, D.B.; Rowshanpour, R.; Saunders, G. J.; Dudding, T.; Yudin, A. K. J. Org. Chem. 2024, 89, 1483-1491. (https://doi.org/10.1021/acs.joc.3c02084)
-Metal Ion-Induced Large Fragment Deactivation: A Different Strategy for Site-Selectivity in a Complex Molecule. Ruskin, J.; Sachs, R. K.; Wang, M.; Dekeyser, R.; Lew, Z.; Williams, P.; Hwang, H.; Majumdar, A.; Dudding, T.; Lectka, T. Angew. Chem. Int. Ed. 2024, e202317070. (https://doi.org/10.1002/anie.202317070)
2023
-Photoactivated Pyridine Directed Fluorination through Hydrogen Atom Transfer. Holt, E.; Ruskin, J.; Garrison, N. G.; Vemulapalli, S.; Lam, W.; Kiame, N.; Henriquez, N.; Borukhova, F.; Williams, J.; Dudding, T.; Lectka, T. J. Org. Chem. 2023, 88, 17538-17543. (https://doi.org/10.1021/acs.joc.3c02146)
- A catalytic one-pot synthesis of sydnone heterocycles with mechanistic insights. Dol, R.; Vemulapaulli, S.; Azeez, O.; Dudding, T. Tetrahedron. 2023, 148, 133704. (https://doi.org/10.1016/j.tet.2023.133704)
- Competition between C-C and C-H Bond Fluorination: A Continuum of Electron Transfer and Hydrogen Atom Transfer Mechanisms. Wang, M.; Rowshanpour, R.; Guan, L.; Ruskin, J.; Nguyen, P. M.; Wang, Y.; Zhang. Q. A.; Liu, B.; Woltornist, R.; Stephens, A. M.; Prasad, A.; Dudding, T.; Lectka, T.; Pitts, C. R. J. Am. Chem. Soc. 2023, 145, 22442-22455. (https://doi.org/10.1021/jacs.3c06477)
- How Do Face-to-Face Stacked Aromatic Rings Activate Each Other to Electrophilic Aromatic Substitution? Kazim, M.; Wang, M.; Vemulapalli, S.; Nguyen, P. M.; Wang, Y.; Siegler, M. A.; Dudding, T.; Lectka, T. Org. Lett. 2023, 25, 23, 4318–4322. (https://doi.org/10.1021/acs.orglett.3c01401)
- Through‐Space, Lone‐pair Promoted Aromatic Substitution: A Relay Mechanism Can Beat out Direct Activation. Kazim, M.; Feng, Z.; Vemulapalli, S.; Siegler, M. A.; Chopra, A.; Nguyen, P. M.; Holl, M. G.; Guan, L.; Dudding, T.; Tantillo, D. J.; Lectka, T. Chem. Eur. J. 2023. (https://doi.org/10.1002/chem.202301550)
- C–C Bond Activation and Demethylenation of Epoxides by Amine Radical Dications. Holt, E.; Garrison, N. G.; Rowshanpour, R.; Kim, J. J.; Henriquez, N.; Lam, W.; Kiame, N.; Williams, J.; Zhao, S.; Dudding, T.; Lectka, T. J. Org. Chem. 2023, 88 ,11, 7597–7600. (https://doi.org/10.1021/acs.joc.3c00605)
- A Secondary Orbital Effect Involving Fluorine Is Responsible for Substrate‐Controlled Diastereodivergence in the Catalyzed Syn Aza‐Henry Reaction of α‐Fluoronitroalkanes. Smajlagic, I.; Johnston, J. N.; Dudding, T. Chem. Eur. J. 2023, 29, 24. (https://doi.org/10.1002/chem.202204066)
2022
- N-Heterocyclic Carbene Organocatalyzed Redox-Active/Ring Expansion Reactions: Mechanistic Insights Unveiling Base Cooperativity. Rowshanpour, R.; Gravel, M.; Dudding, T. J. Org. Chem. 2022, 87, 24, 16785-16793. (https://doi.org/10.1021/acs.joc.2c02462)
- Rational Computational Design of Systems Exhibiting Strong Halogen Bonding Involving Fluorine in Bicyclic Diamine Derivatives. Harry, S. A.; Vemulapalli, S.; Dudding, T.; Lectka, T. J. Org. Chem. 2022, 87, 13, 8413–8419. (https://doi.org/10.1021/acs.joc.2c00497)
- Organocatalysis Linked to Charge-Enhanced Acidity with Superelectrophilic Traits. Smajlagic, I.; White, B.; Azeez, O.; Pilkington, M.; Dudding, T. ACS Catal. 2022, 12, 2, 1128–1138. (https://doi.org/10.1021/acscatal.1c05296)
2021
- Generation and reactivity of an elusive base-stabilised phosphinidene. Nguyen, M. T.; Spasyuk, D.; White, B.; Dudding, T.; Nikonov, G. I. Dalton Trans. 2021, 50, 16613-16619. (https://doi.org/10.1039/D1DT03181C)
- DFT-Based Stereochemical Rationales for the Bifunctional Brønsted Acid/Base-Catalyzed Diastereodivergent and Enantioselective aza-Henry Reactions of α-Nitro Esters. Struble, T. J.; Smajlagic, I.; Foy, H.; Dudding, T; Johnston, J. N., J. Org. Chem. 2021, 86, 21, 15606–15617. (https://doi.org/10.1021/acs.joc.1c02112)
- pKa Scale for Cyclopropenium Ions with Applications in CO2 Capture. Vemulapalli, S.; Guest, M.; Smajlagic, I.; Dudding, T. J. Org. Chem. 2021, 86, 11835−11844. (https://doi.org/10.1021/acs.joc.1c01255)
- Diversity-Oriented Synthesis of Glycomimetics. Meanwell, M.; Fehr1, G.; Ren, W.; Adluri, B.; Rose, V.; Lehmann, J.; Silverman, S. M.; Rowshanpour, R.; Adamson, C.; Bergeron-Brlek, M.; Foy, H.; Challa, V. R.; Campeau, L. C.; Dudding, T.; Britton, R. Nat. Commun. Chem. 2021, 4, 96.
- Brønsted Acid Organocatalyzed Three-Component Hydroamidation Reactions of Vinyl Ethers. Smajlagic, I.; Carlson, B.; Dudding, T. J. Org. Chem. 2021, 86, 4171–4181.
- Azo Synthesis Meets Molecular Iodine Catalysis. Rowshanpour, R.; Dudding, T. RSC Adv. 2021, 11, 7251–7256. (https://doi.org/10.1039/D1RA00369K)
- Oxidative Rearrangement of MIDA (N-Methyliminodiacetic Acid) Boronates: Mechanistic Insights and Synthetic Applications. Kaldas, S. J.; Tien, C-H, Gomes, G.; Meyer, S.; Sirvinskas, M.; Foy, H.; Dudding, T.; Yudin, A. K. Org. Lett. 2021, 23, 324–328.
2020
- Cooperative Noncovalent Interactions Lead to a Highly Diastereoselective Sulfonyl-Directed Fluorination of Steroidal α,β- Unsaturated Hydrazones. Capilato, J. N.; Siegler, M. A.; Rowshanpour, R.; Dudding, T.; Lectka, T. J. Org. Chem. 2020, 86, 1300−1307. (https://doi.org/10.1021/acs.joc.0c02716)
- Trisaminocyclopropenium Cations as Small Molecule Organic Fluorophores: Design Guidelines and Bioimaging Applications. Guest, M.; Mir, R.; Foran, G.; Hickson, B.; Necakov, A.; Dudding, T. J. Org. Chem. 2020, 85, 21, 13997–14011. (https://doi.org/10.1021/acs.joc.0c02026)
- Carbonyl-Directed Aliphatic Fluorination: A Special Type of Hydrogen Atom Transfer Beats Out Norrish II. Ghorbani, F.; Harry, S. A.; Capilato, J. N.; Pitts, C. R.; Joram, J.; Peters, G.; Tovar, J. D.; Smajlagic, I.; Siegler, M. A.; Dudding, T.; Lectka, T. J. Am. Chem. Soc. 2020, 142, 34, 14710–14724.
- DFT Case Study of the Mechanism of a Metal-Free Oxygen Atom Insertion into a p-Quinone Methide C(sp3)–C(sp2) Bond. Smajlagic, I.; Kazim, M.; Lectka, T.; Dudding, T. J. Org. Chem. 2020, 85, 15, 10110-10117.
- Stereoselective Synthesis of N‐Propargyl Alkynes and Axial Chiral N‐Allenes with Epimeric Pyrroloimidazolone Auxiliaries. Sechi, M.; Andrade, M.; Foy, H.; Pilkington, M.; Dudding, T.; Metallinos, C. Adv. Synth. Catal. 2020, 362, 20, 4397-4408.
- Organofluorine Compounds in Fluorine-18 Positron Emission Tomography Imaging. Smajlagic, I.; Rowshanpour, R.; Milkin, L.; Dudding, T. Res. Rev. Health: Open Access J. 2020, 5, 3, 488-491.
- Development of an Unsymmetrical Cyclopropenimine‐Guanidine Platform for Accessing Strongly Basic Proton Sponges and Boron‐Difluoride Diaminonaphthalene Fluorophores. Guest, M.; Le Sueur, R.; Pilkington, M.; Dudding, T. Chem. Eur. J. 2020, 26, 39, 8608-8620. (https://doi.org/10.1002/chem.202001227)
- Site-Selective Photochemical Fluorination of Ketals: Unanticipated Outcomes in Selectivity and Stability. Capilato, J. N.; Pitts, C. R.; Rowshanpour, R.; Dudding, T.; Lectka, T. J. Org. Chem. 2020, 85, 6, 2855–2864. (https://doi.org/10.1021/acs.joc.9b03047)
- Stereoelectronic and Resonance Effects on the Rate of Ring Opening of N-Cyclopropyl-Based Single Electron Transfer Probes. Grimm, M., Suleman N.K.; Hancock, A.N.; Spencer, J.N.; Dudding, T.; Rowshanpour, R.; Castagnoli, N.; Tanko, J.M. J. Am. Chem. Soc. 2020, 142, 5, 2640-2652
2019
- Mechanistic Insight Towards Understanding the Role of Charge in Thiourea Organocatalysis. Smajlagic, I.; Guest, M.; Durán, R.; Herrera, B.; Dudding, T. J. Org. Chem. 2019, 85, 585-593. (https://doi.org/10.1021/acs.joc.9b02682)
- Charge-enhanced thiourea catalysts as hydrogen bond donors for Friedel‒Crafts Alkylations. Smajlagic, I.; Carlson, B.; Rosano, N.; Foy, H.; Dudding, T. Tetrahedron, 2019, 75, 130757-130764. (https://doi.org/10.1016/j.tet.2019.130757)
- Discovery and Mechanistic Study of a Totally Organic C(aryl)-C(alkyl) Oxygen Insertion Reaction. Kazim, M.; Foy, H.; Siegler, M.A.; Dudding, T.; Lectka, T. J. Org. Chem. 2019, 84, 21, 14349-14353.
- Ligand Effect in Alkali Metal‐Catalyzed Transfer Hydrogenation of Ketones. Alshakova, I.D.; Foy, H.; Dudding, T.; Nikonov, G.I. Chem. Euro. J. 2019, 25, 11734-11744.
- Competitive hydrogen bonding of cyclopropenium ions: Implications of an anion switch. Le Sueur, R.; Guest, M.; Belding, L.; Pilkington, M.; Dudding, T. Tetrahedron Lett. 2019, 60, 150928-150931.
- Direct Observation and Analysis of the Halo-Amino-Nitro Alkane Functional Group. Crocker, M.; Foy, H.; Tokumaru, K.; Dudding, T.; Pink, M.; Johnston, J. Chem. 2019, 5, 1248-1264.
- Selective Aerobic Oxidation of Benzylic Alcohols Catalyzed by a Dicyclopropenylidene-Ag(I) Complex. Mir, R.; Rowhsanpour, R.; Dempsey, K.; Pilkington, M.; Dudding T. J. Org. Chem. 2019, 84, 5726-5731.
- A mechanistic study of oxygen atom transfer from N-sulfonyloxaziridine to enolates. Foy, H.; Schwan, A.; Dudding, T. Tetrahedron 2019, 75, 2056-2061.
2018
- Cyclopropenium Enhanced Thiourea Catalysis. Smajlagic, I.; Duran, R.; Pilkington, M.; Dudding, T. J. Org. Chem. 2018, 83, 13973-13980. (https://doi.org/10.1021/acs.joc.8b02321)
- Synthesis of α‑Borylated Ketones by Regioselective Wacker Oxidation of Alkenylboronates. Corless, V.; Holownia, A.; Foy, H.; Mendoza-Sanchez, R.; Adachi, S.; Dudding, T.; Yudin, A. Org. Lett. 2018, 20, 5300 - 5303.
- Amine hemilability enables boron to mechanistically resemble either hydride or proton. Lee, F.; Diaz, D.; Holownia, A.; Kaldas, S.; Liew, S.; Garrett, G.; Dudding, T.; Yudin, A. Nat. Chem. 2018, 10, 1062-1070.
- A Mechanistic Model for the Aziridine Aldehyde-driven Macrocyclization of Peptides. Belding, L.; Zaretsky, S.; Yudin, A. K.; Dudding, T. J. Org. Chem. 2018, 83, 9119-9124.
- Fluorescence of Cyclopropenium Ion Derivatives. Belding, L.; Guest, M.; Le Sueur, R.; Dudding, T. J. Org. Chem. 2018, 83, 6489-6497. (https://doi.org/10.1021/acs.joc.8b00770)
- Expanding the repertoire of cyclopropenium ion phase transfer catalysis: Benzylic fluorination. Dempsey, K.; Mir, R.; Smajlagic, I.; Dudding, T. Tetrahedron. 2018, 74, 3507-3511.
- Bis (amino) cyclopropenium Trifluoroborates: Synthesis, Hydrolytic Stability Studies, and DFT Insights. Mir, R.; Dudding, T. J. Org. Chem. 2018, 83, 4384-4388.
2017
- Zinc-Catalyzed Hydrosilylation and Hydroboration of N-Heterocycles. Lortie, J.L.; Dudding, T.; Gabidullin, B.M.; Nikonov, G.I. ACS. Catal. 2017, 7, 8454-8459.
- Phase-Transfer Catalyzed O-Silyl Ether Deprotection Mediated by a Cyclopropenium Cation. Mir, R.; Dudding, T. J. Org. Chem. 2017, 82, 709-714.
2016
- Investigation of a new chiral auxiliary derived chemoenzymatically from toluene: experimental and computational study. Snajdr, I.; Froese, J.; Dudding, T.; Horakova, P.; Hudlicky, T. Can. J. Chem. 2016, 94, 848-856.
- Unique molecular geometries of reduced 4-and 5-coordinate zinc complexes stabilised by diiminopyridine ligand. Chu, T.; Belding, L.; Poddutoori, P. K.; van der Est, A.; Dudding, T.; Korobkov, I.; Nikonov, G. I. Dalton Trans. 2016, 45, 13440-13448.
- A Au(I)-Precatalyst with a Cyclopropenium Counterion: An Unusual Ion Pair. Mir, R.; Dudding, T. J. Org. Chem. 2016, 81, 2675-2679.
- An Evolving Insight into Chiral H-Bond Catalyzed Aza-Henry Reactions: A Cooperative Role for Noncovalent Attractive Interactions Unveiled by Density Functional Theory. Taimoory, S. M.; Dudding, T. J. Org. Chem. 2016, 81, 3286-3295.
- Phase-Transfer Catalysis via a Proton Sponge: A Bifunctional Role for Biscyclopropenimine. Belding, L. Stoyanov, P. Dudding, T. J. Org. Chem. 2016, 81, 553-558.
- Synthesis, Theoretical Analysis, and Experimental pKa Determination of a Fluorescent, Nonsymmetric, In Out Proton Sponge. Belding, L. Stoyanov, P. Dudding, T. J. Org. Chem. 2016, 81, 6-13. (doi.org/10.1021/acs.joc.5b01743)
-Polymer-Supported Strong Lewis Acid Phosphonium Cation Catalysis Applied to Sydnone Synthesis. Dol, R. Kovljenic, N.; Dudding, T. Chem. Commun. 2024, ASAP. (https://doi.org/10.1039/D4CC03412K)
- Complementary Tandem Reaction Manifolds and "Switch Mechanisms" in the Reaction of Epoxides with Selectfluor. Garrison, N. G.; Holt, E.; Wang, M.; Rowshanpour, R.; Kiame, N.; Lam, W.; Borukhova, F.; Dudding, T.; Lectka, T. J. Org. Chem. 2024, ASAP. (doi.org/10.1021/acs.joc.4c01470)
- A Rigidified Macrocyclic Grubbs Complex: A Rare Example of In- and Out-Isomers that Show a Dramatic Difference in Catalytic Reactivity. Davalos-Moringo, A. R.; Vemulapalli, S.; Dudding, T.; Diver, S. T. Organometallics 2024, ASAP. (doi.org/10.1021/acs.organomet.4c00331)
- Streamlining Fluoroalkenyl Arene Synthesis Illuminated with Mechanistic Insights. Rajabalinia, S.; Hoford, S.; Dudding, T. ACS Omega 2024, 9, 21152-21163. (https://doi.org/10.1021/acsomega.4c01055)
- Catalytic Light-Driven Strategy for Transforming Oximes to Carbonyls. White, B.; Dudding, T. J. Org. Chem. 2024, 89, 4569-4578. (https://doi.org/10.1021/acs.joc.3c02793)
-A Boron Scan of Ethyl Acetoacetate Leads to Versatile Building Blocks. Trofimova, A.; White, B.; Diaz, D. B.; Sirvinskas, M. J.; Lough, A.; Dudding, T.; Yudin, A. K. Angew. Chem. Int. Ed. 2024, e202319842. (https://doi.org/10.1002/anie.202319842)
-The Role of Attractive Non-Covalent Interactions in Peptide Macrocyclization. Diaz, D.B.; Rowshanpour, R.; Saunders, G. J.; Dudding, T.; Yudin, A. K. J. Org. Chem. 2024, 89, 1483-1491. (https://doi.org/10.1021/acs.joc.3c02084)
-Metal Ion-Induced Large Fragment Deactivation: A Different Strategy for Site-Selectivity in a Complex Molecule. Ruskin, J.; Sachs, R. K.; Wang, M.; Dekeyser, R.; Lew, Z.; Williams, P.; Hwang, H.; Majumdar, A.; Dudding, T.; Lectka, T. Angew. Chem. Int. Ed. 2024, e202317070. (https://doi.org/10.1002/anie.202317070)
2023
-Photoactivated Pyridine Directed Fluorination through Hydrogen Atom Transfer. Holt, E.; Ruskin, J.; Garrison, N. G.; Vemulapalli, S.; Lam, W.; Kiame, N.; Henriquez, N.; Borukhova, F.; Williams, J.; Dudding, T.; Lectka, T. J. Org. Chem. 2023, 88, 17538-17543. (https://doi.org/10.1021/acs.joc.3c02146)
- A catalytic one-pot synthesis of sydnone heterocycles with mechanistic insights. Dol, R.; Vemulapaulli, S.; Azeez, O.; Dudding, T. Tetrahedron. 2023, 148, 133704. (https://doi.org/10.1016/j.tet.2023.133704)
- Competition between C-C and C-H Bond Fluorination: A Continuum of Electron Transfer and Hydrogen Atom Transfer Mechanisms. Wang, M.; Rowshanpour, R.; Guan, L.; Ruskin, J.; Nguyen, P. M.; Wang, Y.; Zhang. Q. A.; Liu, B.; Woltornist, R.; Stephens, A. M.; Prasad, A.; Dudding, T.; Lectka, T.; Pitts, C. R. J. Am. Chem. Soc. 2023, 145, 22442-22455. (https://doi.org/10.1021/jacs.3c06477)
- How Do Face-to-Face Stacked Aromatic Rings Activate Each Other to Electrophilic Aromatic Substitution? Kazim, M.; Wang, M.; Vemulapalli, S.; Nguyen, P. M.; Wang, Y.; Siegler, M. A.; Dudding, T.; Lectka, T. Org. Lett. 2023, 25, 23, 4318–4322. (https://doi.org/10.1021/acs.orglett.3c01401)
- Through‐Space, Lone‐pair Promoted Aromatic Substitution: A Relay Mechanism Can Beat out Direct Activation. Kazim, M.; Feng, Z.; Vemulapalli, S.; Siegler, M. A.; Chopra, A.; Nguyen, P. M.; Holl, M. G.; Guan, L.; Dudding, T.; Tantillo, D. J.; Lectka, T. Chem. Eur. J. 2023. (https://doi.org/10.1002/chem.202301550)
- C–C Bond Activation and Demethylenation of Epoxides by Amine Radical Dications. Holt, E.; Garrison, N. G.; Rowshanpour, R.; Kim, J. J.; Henriquez, N.; Lam, W.; Kiame, N.; Williams, J.; Zhao, S.; Dudding, T.; Lectka, T. J. Org. Chem. 2023, 88 ,11, 7597–7600. (https://doi.org/10.1021/acs.joc.3c00605)
- A Secondary Orbital Effect Involving Fluorine Is Responsible for Substrate‐Controlled Diastereodivergence in the Catalyzed Syn Aza‐Henry Reaction of α‐Fluoronitroalkanes. Smajlagic, I.; Johnston, J. N.; Dudding, T. Chem. Eur. J. 2023, 29, 24. (https://doi.org/10.1002/chem.202204066)
2022
- N-Heterocyclic Carbene Organocatalyzed Redox-Active/Ring Expansion Reactions: Mechanistic Insights Unveiling Base Cooperativity. Rowshanpour, R.; Gravel, M.; Dudding, T. J. Org. Chem. 2022, 87, 24, 16785-16793. (https://doi.org/10.1021/acs.joc.2c02462)
- Rational Computational Design of Systems Exhibiting Strong Halogen Bonding Involving Fluorine in Bicyclic Diamine Derivatives. Harry, S. A.; Vemulapalli, S.; Dudding, T.; Lectka, T. J. Org. Chem. 2022, 87, 13, 8413–8419. (https://doi.org/10.1021/acs.joc.2c00497)
- Organocatalysis Linked to Charge-Enhanced Acidity with Superelectrophilic Traits. Smajlagic, I.; White, B.; Azeez, O.; Pilkington, M.; Dudding, T. ACS Catal. 2022, 12, 2, 1128–1138. (https://doi.org/10.1021/acscatal.1c05296)
2021
- Generation and reactivity of an elusive base-stabilised phosphinidene. Nguyen, M. T.; Spasyuk, D.; White, B.; Dudding, T.; Nikonov, G. I. Dalton Trans. 2021, 50, 16613-16619. (https://doi.org/10.1039/D1DT03181C)
- DFT-Based Stereochemical Rationales for the Bifunctional Brønsted Acid/Base-Catalyzed Diastereodivergent and Enantioselective aza-Henry Reactions of α-Nitro Esters. Struble, T. J.; Smajlagic, I.; Foy, H.; Dudding, T; Johnston, J. N., J. Org. Chem. 2021, 86, 21, 15606–15617. (https://doi.org/10.1021/acs.joc.1c02112)
- pKa Scale for Cyclopropenium Ions with Applications in CO2 Capture. Vemulapalli, S.; Guest, M.; Smajlagic, I.; Dudding, T. J. Org. Chem. 2021, 86, 11835−11844. (https://doi.org/10.1021/acs.joc.1c01255)
- Diversity-Oriented Synthesis of Glycomimetics. Meanwell, M.; Fehr1, G.; Ren, W.; Adluri, B.; Rose, V.; Lehmann, J.; Silverman, S. M.; Rowshanpour, R.; Adamson, C.; Bergeron-Brlek, M.; Foy, H.; Challa, V. R.; Campeau, L. C.; Dudding, T.; Britton, R. Nat. Commun. Chem. 2021, 4, 96.
- Brønsted Acid Organocatalyzed Three-Component Hydroamidation Reactions of Vinyl Ethers. Smajlagic, I.; Carlson, B.; Dudding, T. J. Org. Chem. 2021, 86, 4171–4181.
- Azo Synthesis Meets Molecular Iodine Catalysis. Rowshanpour, R.; Dudding, T. RSC Adv. 2021, 11, 7251–7256. (https://doi.org/10.1039/D1RA00369K)
- Oxidative Rearrangement of MIDA (N-Methyliminodiacetic Acid) Boronates: Mechanistic Insights and Synthetic Applications. Kaldas, S. J.; Tien, C-H, Gomes, G.; Meyer, S.; Sirvinskas, M.; Foy, H.; Dudding, T.; Yudin, A. K. Org. Lett. 2021, 23, 324–328.
2020
- Cooperative Noncovalent Interactions Lead to a Highly Diastereoselective Sulfonyl-Directed Fluorination of Steroidal α,β- Unsaturated Hydrazones. Capilato, J. N.; Siegler, M. A.; Rowshanpour, R.; Dudding, T.; Lectka, T. J. Org. Chem. 2020, 86, 1300−1307. (https://doi.org/10.1021/acs.joc.0c02716)
- Trisaminocyclopropenium Cations as Small Molecule Organic Fluorophores: Design Guidelines and Bioimaging Applications. Guest, M.; Mir, R.; Foran, G.; Hickson, B.; Necakov, A.; Dudding, T. J. Org. Chem. 2020, 85, 21, 13997–14011. (https://doi.org/10.1021/acs.joc.0c02026)
- Carbonyl-Directed Aliphatic Fluorination: A Special Type of Hydrogen Atom Transfer Beats Out Norrish II. Ghorbani, F.; Harry, S. A.; Capilato, J. N.; Pitts, C. R.; Joram, J.; Peters, G.; Tovar, J. D.; Smajlagic, I.; Siegler, M. A.; Dudding, T.; Lectka, T. J. Am. Chem. Soc. 2020, 142, 34, 14710–14724.
- DFT Case Study of the Mechanism of a Metal-Free Oxygen Atom Insertion into a p-Quinone Methide C(sp3)–C(sp2) Bond. Smajlagic, I.; Kazim, M.; Lectka, T.; Dudding, T. J. Org. Chem. 2020, 85, 15, 10110-10117.
- Stereoselective Synthesis of N‐Propargyl Alkynes and Axial Chiral N‐Allenes with Epimeric Pyrroloimidazolone Auxiliaries. Sechi, M.; Andrade, M.; Foy, H.; Pilkington, M.; Dudding, T.; Metallinos, C. Adv. Synth. Catal. 2020, 362, 20, 4397-4408.
- Organofluorine Compounds in Fluorine-18 Positron Emission Tomography Imaging. Smajlagic, I.; Rowshanpour, R.; Milkin, L.; Dudding, T. Res. Rev. Health: Open Access J. 2020, 5, 3, 488-491.
- Development of an Unsymmetrical Cyclopropenimine‐Guanidine Platform for Accessing Strongly Basic Proton Sponges and Boron‐Difluoride Diaminonaphthalene Fluorophores. Guest, M.; Le Sueur, R.; Pilkington, M.; Dudding, T. Chem. Eur. J. 2020, 26, 39, 8608-8620. (https://doi.org/10.1002/chem.202001227)
- Site-Selective Photochemical Fluorination of Ketals: Unanticipated Outcomes in Selectivity and Stability. Capilato, J. N.; Pitts, C. R.; Rowshanpour, R.; Dudding, T.; Lectka, T. J. Org. Chem. 2020, 85, 6, 2855–2864. (https://doi.org/10.1021/acs.joc.9b03047)
- Stereoelectronic and Resonance Effects on the Rate of Ring Opening of N-Cyclopropyl-Based Single Electron Transfer Probes. Grimm, M., Suleman N.K.; Hancock, A.N.; Spencer, J.N.; Dudding, T.; Rowshanpour, R.; Castagnoli, N.; Tanko, J.M. J. Am. Chem. Soc. 2020, 142, 5, 2640-2652
2019
- Mechanistic Insight Towards Understanding the Role of Charge in Thiourea Organocatalysis. Smajlagic, I.; Guest, M.; Durán, R.; Herrera, B.; Dudding, T. J. Org. Chem. 2019, 85, 585-593. (https://doi.org/10.1021/acs.joc.9b02682)
- Charge-enhanced thiourea catalysts as hydrogen bond donors for Friedel‒Crafts Alkylations. Smajlagic, I.; Carlson, B.; Rosano, N.; Foy, H.; Dudding, T. Tetrahedron, 2019, 75, 130757-130764. (https://doi.org/10.1016/j.tet.2019.130757)
- Discovery and Mechanistic Study of a Totally Organic C(aryl)-C(alkyl) Oxygen Insertion Reaction. Kazim, M.; Foy, H.; Siegler, M.A.; Dudding, T.; Lectka, T. J. Org. Chem. 2019, 84, 21, 14349-14353.
- Ligand Effect in Alkali Metal‐Catalyzed Transfer Hydrogenation of Ketones. Alshakova, I.D.; Foy, H.; Dudding, T.; Nikonov, G.I. Chem. Euro. J. 2019, 25, 11734-11744.
- Competitive hydrogen bonding of cyclopropenium ions: Implications of an anion switch. Le Sueur, R.; Guest, M.; Belding, L.; Pilkington, M.; Dudding, T. Tetrahedron Lett. 2019, 60, 150928-150931.
- Direct Observation and Analysis of the Halo-Amino-Nitro Alkane Functional Group. Crocker, M.; Foy, H.; Tokumaru, K.; Dudding, T.; Pink, M.; Johnston, J. Chem. 2019, 5, 1248-1264.
- Selective Aerobic Oxidation of Benzylic Alcohols Catalyzed by a Dicyclopropenylidene-Ag(I) Complex. Mir, R.; Rowhsanpour, R.; Dempsey, K.; Pilkington, M.; Dudding T. J. Org. Chem. 2019, 84, 5726-5731.
- A mechanistic study of oxygen atom transfer from N-sulfonyloxaziridine to enolates. Foy, H.; Schwan, A.; Dudding, T. Tetrahedron 2019, 75, 2056-2061.
2018
- Cyclopropenium Enhanced Thiourea Catalysis. Smajlagic, I.; Duran, R.; Pilkington, M.; Dudding, T. J. Org. Chem. 2018, 83, 13973-13980. (https://doi.org/10.1021/acs.joc.8b02321)
- Synthesis of α‑Borylated Ketones by Regioselective Wacker Oxidation of Alkenylboronates. Corless, V.; Holownia, A.; Foy, H.; Mendoza-Sanchez, R.; Adachi, S.; Dudding, T.; Yudin, A. Org. Lett. 2018, 20, 5300 - 5303.
- Amine hemilability enables boron to mechanistically resemble either hydride or proton. Lee, F.; Diaz, D.; Holownia, A.; Kaldas, S.; Liew, S.; Garrett, G.; Dudding, T.; Yudin, A. Nat. Chem. 2018, 10, 1062-1070.
- A Mechanistic Model for the Aziridine Aldehyde-driven Macrocyclization of Peptides. Belding, L.; Zaretsky, S.; Yudin, A. K.; Dudding, T. J. Org. Chem. 2018, 83, 9119-9124.
- Fluorescence of Cyclopropenium Ion Derivatives. Belding, L.; Guest, M.; Le Sueur, R.; Dudding, T. J. Org. Chem. 2018, 83, 6489-6497. (https://doi.org/10.1021/acs.joc.8b00770)
- Expanding the repertoire of cyclopropenium ion phase transfer catalysis: Benzylic fluorination. Dempsey, K.; Mir, R.; Smajlagic, I.; Dudding, T. Tetrahedron. 2018, 74, 3507-3511.
- Bis (amino) cyclopropenium Trifluoroborates: Synthesis, Hydrolytic Stability Studies, and DFT Insights. Mir, R.; Dudding, T. J. Org. Chem. 2018, 83, 4384-4388.
2017
- Zinc-Catalyzed Hydrosilylation and Hydroboration of N-Heterocycles. Lortie, J.L.; Dudding, T.; Gabidullin, B.M.; Nikonov, G.I. ACS. Catal. 2017, 7, 8454-8459.
- Phase-Transfer Catalyzed O-Silyl Ether Deprotection Mediated by a Cyclopropenium Cation. Mir, R.; Dudding, T. J. Org. Chem. 2017, 82, 709-714.
2016
- Investigation of a new chiral auxiliary derived chemoenzymatically from toluene: experimental and computational study. Snajdr, I.; Froese, J.; Dudding, T.; Horakova, P.; Hudlicky, T. Can. J. Chem. 2016, 94, 848-856.
- Unique molecular geometries of reduced 4-and 5-coordinate zinc complexes stabilised by diiminopyridine ligand. Chu, T.; Belding, L.; Poddutoori, P. K.; van der Est, A.; Dudding, T.; Korobkov, I.; Nikonov, G. I. Dalton Trans. 2016, 45, 13440-13448.
- A Au(I)-Precatalyst with a Cyclopropenium Counterion: An Unusual Ion Pair. Mir, R.; Dudding, T. J. Org. Chem. 2016, 81, 2675-2679.
- An Evolving Insight into Chiral H-Bond Catalyzed Aza-Henry Reactions: A Cooperative Role for Noncovalent Attractive Interactions Unveiled by Density Functional Theory. Taimoory, S. M.; Dudding, T. J. Org. Chem. 2016, 81, 3286-3295.
- Phase-Transfer Catalysis via a Proton Sponge: A Bifunctional Role for Biscyclopropenimine. Belding, L. Stoyanov, P. Dudding, T. J. Org. Chem. 2016, 81, 553-558.
- Synthesis, Theoretical Analysis, and Experimental pKa Determination of a Fluorescent, Nonsymmetric, In Out Proton Sponge. Belding, L. Stoyanov, P. Dudding, T. J. Org. Chem. 2016, 81, 6-13. (doi.org/10.1021/acs.joc.5b01743)
2015 and EARLIER
- Enantioselective synthesis of mosquito oviposition pheromone and its epimer from a naturally occurring fatty acid. Hurem, D.; Dudding, T. RSC Advances, 2015, 5, 101732-101739.
- Design and synthesis of a chiral seven-membered ring guanidine organocatalyst applied to asymmetric vinylogous aldol reactions.Mirabdolbaghi, R.; Hassan, M.; Dudding, T. Tetrahedron: Asymmetry 2015, 26, 560-566.
- Expanding the Forefront of Strong Organic Bronsted Acids: Proton Catalyzed Hydroamination of Unactivated Alkenes and Activation of Au(I) for Alkyne Hydroamination. Mirabdolbaghi, R.; Dudding, T. Org. Lett. 2015, 17, 1930-1933.
- Mirroring Enzymes: The Role of Hydrogen Bonding in an Asymmetric Organocatalyzed Aza Henry Reaction - a DFT Study. Belding, L.; Taimoory, S. M.; Dudding, T. ACS Catal. 2014, 5, 343-349.
- Shifting the Energy Landscape of Multicomponent Reactions Using Aziridine Aldehyde Dimers: A Mechanistic Study. Belding, L.; Zaretsky, S.; Rotstein, B. H.; Yudin, A. K.; Dudding, T. J. Org. Chem. 2014, 79, 9469-9471.
- Hydroxyproline-Derived Pseudoenantiomeric [2.2.1] Bicyclic Phosphines: Asymmetric Synthesis of (+)- and (-)-Pyrrolines. Henry, C. E.; Xu, Q.; Chio Fan, Y.; Martin, T. J.; Belding, L.; Dudding, T.; Kwon, O. J. Am. Chem. Soc.2014, 136, 11890-11893.
- A Class of Phase-Transfer Catalyst with Interionic Strain: Insight into the Bonding of Disubstituted N- vs Carbene-Stabilized NI-Centered Cations. Mirabdolbaghi, R.; Dudding, T. Org. Lett. 2014, 16, 2790-2793.
- Diastereodivergent total synthesis of mosquitooviposition pheromone. Hurem, D.; Dudding, T. RSC Adv. 2014, 4, 15552-15557.
- A Coordination Compound of Ge0 Stabilized by a Diiminopyridine Ligand. Chu, T.; Belding, L.; van der Est, A.; Dudding, T.; Korobvoc, I.; Nikonov, G. Angew. Chimie Int. Ed. 2014, 53, 2711-2715.
- Synthesis and Theoretical Investigation of a 1,8-Bis(bis(diisopropylamino)cyclopropeniminyl)naphthalene Proton Sponge Derivative. Belding, L.; Dudding, T. Chem. Eur. J. 2014, 20, 1032-1037.
- A Computational Study of the Copper(II)-Catalyzed Enantioselective Intramolecular Aminooxygenation of Alkenes. Belding, L.; Chemler, S. R.; Dudding, T. J. Org. Chem. 2013, 78, 10288–10297.
- A Detailed NMR- and DFT-Based Study of the Sakurai-Hosomi-Yamamoto Asymmetric Allylation Reaction. Hurem, D.; Moiseev, A. G.; Simionescu, R.; Dudding, T. J. Org. Chem. 2013, 78, 4440-4445.
- A synthetic route to chiral C(3)-functionalized phthalides via a Ag(I)-catalyzed allylation/transesterification sequence. Mirabdolbaghi, R.; Dudding, T. Tetrahedron 2013, 69, 3287-3292.
- Reversal of Stereoselectivity in Lithiation of Ferrocenyl-imidazolones: Epimeric Substrates lead to Planar Chiral Enantiomers. Metallinos, C.; John, J.; Nelson, J.; Dudding, T.; Belding, L. Adv. Synth. Catal. 2013, 335, 1211-1219.
- The application of D-Chiro-inositol as a chiral template for the Diels-Alder reaction. Trant, J. F.; Belding, L.; Dudding, T.; Hudlicky, T. Helvetica Chimica Acta. 2012, 95, 2026-2035.
- An Indium-mediated allylative/transesterification DFT-directed approach to chiral C(3)-functionalized phthalides. Mirabdolbaghi, R.; Dudding, T. Org. Lett. 2012, 14, 3748-3751.
- Studies on the ring opening reactions of 3-oxa-1-azabicyclo[3.1.0]hexan-2-ones. Synthesis of aminomethyl oxazolidinones and aziridinyl ureas. Wells, G. M.; Dudding, T.; Belding, L.; Frick, A. J.; Nayek, A.; Huang, J.; Katz, S. J; Bergmeier, S. C. Tetrahedron 2012, 68, 3980-3987.
- Characterization of highly unusual NH-O hydrogen bonding to ester ether oxygen atoms through spectroscopic, kinetic and computational studies. Scerba, M. T.; Deblase, A. F.; Bloom, S.; Dudding, T. C.; Johnson, M. A.; Lectka, T. J. Phys. Chem. A. 2012, 116, 3556-3560.
- A catalytic asymmetric approach to C1-chiral 3-methylene-indan-1-ols. Mirabdolbaghi, R.; Dudding, T. Tetrahedron 2012, 68, 1988-1991.
- Evidence for alkene cis-aminocupration, an aminooxygenation case study: Kinetics, EPR spectroscopy and DFT calculations. Paderes, M. C.; Belding, L.; Fonovic, B.; Dudding, T.; Keister, J. B; Chemler, S. R. Chem. - Eur. J. 2011, 18, 1711-1726.
- Directed ortho,ortho'-dimetalation of hydrobenzoin: Rapid access to hydrobenzoin derivatives useful for asymmetric synthesis. Cho, I.; Meimetis, L.; Belding, L.; M. J. Katz; Dudding, T.; Britton, R. Beilstein J. Org. Chem. 2011, 7, 1315-1322.
- From bifunctional to trifunctional (tricomponent nucleophile-transition metal-Lewis acid) catalysis: The catalytic, enantioselective a-fluorination of acid chlorides. Erb, J.; Paull, D. H.; Dudding, T.; Belding, L.; Lectka, T. J. Am. Chem. Soc. 2011, 133, 7536-7546.
- NHC-catalyzed intramolecular redox amidation for the synthesis of functionalized lactams: Evidence of hydrogen bonding co-catalysis. Thai, K.; Wang, L.; Dudding, T.; Bilodeau, F.; Gravel, M. Org. Lett. 2010, 12, 5708-5711.
- Asymmetric lithiation of boron trifluoride-activated aminoferrocenes: An experimental and computational investigation. Metallinos, C.; Zaifman, J.; Dudding, T.; Van Belle, L.; Taban, K. Adv. Synth. & Catal. 2010, 352, 1967-1982.
- Desymmetrizations forming tetrasubstituted olefins using enantioselective olefin metathesis. Stenne, B.; Timperio, J.; Savoie, J.; Dudding, T.; Collins, S. K. Org. Lett. 2010, 12, 2032-2035.
- The enzymatic cleavage of Si-O bonds: A kinetic analysis of the biocatalyzed hydrolysis of phenyltrimethoxysilane. Frampton, M. B.; Simionescu, R.; Dudding, T.; Zelisko, P. M. J. Molecular Catalysis B: J. Mol. Catal. B: Enzym. 2010, 66, 105-112.
- Incorporation of 2,3-disubstituted-1,4-naphthoquinones into the A1 binding site of photosystem I studied by EPR and ENDOR spectroscopy. van der Est, A.; Pushkar, Y.; Karyagina, I.; Fonovic, B.; Dudding, T.; Niklas, J.; Lubitz, W.; Golbeck, J. H. Appl. Magn. Reson. 2009, 37, 65-83.
- New options for the reactivity of the Burgess reagent with epoxides in both racemic and chiral auxiliary modes structural and mechanistic revisions, computational studies, and application to synthesis. Leisch, H.; Sullivan, B.; Fonovic, B.; Dudding, T.; Hudlicky, T. Eur. J. Org. Chem. 2009, 17, 2806-2819.
- Inverse temperature dependence in the diastereoselective addition of Grignard reagents to a tetrahydrofurfural. Mowat, J.; Kang, B.; Fonovic, B.; Dudding, T.; Britton, R. Org. Lett. 2009, 11, 2057-2060.
- A surprising mechanistic 'switch' in Lewis acid activation: A bifunctional, asymmetric approach to a-hydroxy acid derivatives. Abraham, C. J.; Paull, D. H.; Bekele, T.; Scerba, M. T.; Dudding, T.; Lectka, T. J. Am. Chem. Soc. 2008, 130, 17085-17094.
- Origin of enantioselection in hetero-Diels-Alder reactions catalyzed by naphthyl-TADDOL. Anderson, C. D.; Dudding, T.; Gordillo, R; Houk, K. N. Org. Lett. 2008, 10, 2749-2752.
- Theory-guided design of Bronsted acid-assisted phosphine catalysis: synthesis of dihydropyrones from aldehydes and allenoates. Creech, G.S.; Zhu, X.F.; Fonovic, B.; Dudding, T.; Kwon, O. Tetrahedron 2008, 64, 6935-3942.
- Phosphine triggered [3 + 2] allenoate-acrylate annulation: A mechanistic enlightenment. Mercier, E.; Fonovic, B.; Henry, C.; Kwon, O.; Dudding, T. Tetrahedron Lett. 2007, 48, 3617-3620.
- A mechanistic study on the catalytic, asymmetric α-bromination of acid chlorides. Dogo-Isonagie, C; Bekele, T.; France, S.; Wolfer, S.; Weatherwax, A.; Taggi, A. E.; Paull, D. H.; Dudding, T.; Lectka, T. Eur. J. Org. Chem. 2007, 7, 1091-1100.
- Hydrogen-bonding catalysis induces a change in mechanism of polar Diels-Alder reactions. Gordillo, R; Dudding, T.; Anderson, C. D.; Houk, K. N. Org. Lett. 2007, 9, 501-503.
- An Experimental and theoretical study of the asymmetric lithiation of 1,2,3,5,6,7-hexahydro-3α,4α-diazacyclopenta[def]phenanthren-4-one. Metallinos, C.; Dudding, T.; Zaifman, J.; Chaytor, J. L.; Taylor, N. J. J. Org. Chem. 2007, 72, 957-963.
- Trypsin-catalyzed cross-linking of α,ω;-triethoxysilyl-terminated polydimethylsiloxane: an experimental and computational approach. Zelisko, P. M.; Dudding, T.; Amelien, K. R.; Stanisic, H. Polymer Preprints 2007, 48, 984.
- Theoretical rationale for regioselection in phosphine catalyzed allenoate additions to acrylates, imines and aldehdyes. Dudding, T.; Kwon, O.; Mercier, E. Org. Lett. 2006, 8, 3643-3646.
- Phosphine-Catalyzed Synthesis of 1,3-Dioxan-4-ylidenes. Zhu, X-F; Henry, C. E.; Wang, J.; Dudding, T.; Kwon, O. Org. Lett. 2005, 7, 1387-1390.
- Computational Predictions of Stereochemistry in Asymmetric Thiazolium and Triazolium Catalyzed Benzoin Condensations. Dudding, T.; Houk, K. N. Proc. Natl. Acad. Sci. U.S.A. 2004, 101, 5770-5775.
- A Multistage, One-Pot Procedure Mediated by a Single Catalyst: A New Approach to the Catalytic Asymmetric Synthesis of Alpha-Amino Acids. Hafez, A. M.; Dudding, T.; Wagerle, T. R.; Shah, M. H.; Taggi, A. E.; Lectka, T. J. Org. Chem. 2003, 68, 5819-5825.
- Molecular Mechanics Calculations as Predictors of Enantioselectivity for Chiral Nucleophile Catalyzed Reactions. Taggi, A. E.; Hafez, A. M.; Dudding, T.; Lectka, T. Tetrahedron 2002, 58, 8351-8356.
- A Structure-Activity Study of Spermicidal and anti-HIV properties of Hydroxylated Cationic Surfactants. Wong, Yue Ling; Hubieki, M.; Curfman, C. L.; Doncel, G. F.; Dudding, T. C.; Savle, P. S.; Gandour, R. D. Bioorganic & Medicinal Chemistry 2002, 10, 3599-3608.
- A Catalyst that Plays Multiple Roles: Asymmetric Synthesis of -Substituted Aspartic Acid Derivatives through a Four-Stage, One-Pot Procedure. Dudding, T.; Hafez, A. M.; Taggi, A. E.; Wagerle, T. R.; Lectka, T. Org. Lett. 2002, 4, 387-390.
- Catalytic, Enantioselective Alkylation of -Imino Esters Derivatives. Ferraris, D.; Young, B.; Cox, C.; Dudding, T.; Drury, W.J. III; Ryzhkov, L.; Taggi, A. E.; Lectka, T. J. Am. Chem. Soc. 2002, 124, 67-77.
- Spermicidal, Anti-HIV, and Micellar Properties of Di- and Trihydroxylated Cationic Surfactants. Wong, Yue-Ling; Curfman, C. L.; Doncel, G. F.; Hubieki, M. P.; Dudding, T. C.; Savle, P. S.; Gandour, R. D. Tetrahedron 2002, 58, 45-54.
- Asymmetric Catalysis on Sequentially-linked Columns. Hafez, A. M.; Taggi, A. E.; Dudding, T.; Lectka, T. J. Am. Chem. Soc. 2001, 123, 10853-10859.
- Base- and Acid-catalyzed Interconversions of O-acyl- and N-acyl-ethanolamines: A Cautionary Note for Lipid Analysis. Markey, S. P.; Dudding, T.; Wang, Tao-Chin L. J. Lipid Research 2000, 41, 657-662.
- Catalytic, Enantioselective Alkylation of N,O- and N,N-Acetals and Hemiacetals. Ferraris, D.; Young, B.; Dudding, T.; Drury, W. J. III; Lectka, T. Tetrahedron 1999, 55, 8869-8882.
- Catalytic Enantioselective Alkylation Reactions of N,O-Acetals. Ferraris, D.; Young, B.; Dudding, T.; Drury, W. J. III; Lectka, T. J. Org. Chem. 1999, 64, 2168-2169.
- Diastereo- and Enantioselective Alkylation of Alpha-Imino Esters with Cyclic Enol Silanes Catalyzed by (R)-Tol-BINAP-CuClO4•(MeCN)2. Ferraris, D.; Young, B.; Cox, C.; Drury, W. J. III; Dudding, T.; Lectka, T. J. Org. Chem. 1998, 63, 6090-6091.
- Catalytic, Enantioselective Alkylation of Alpha-Imino Esters Using Late Transition Metal Phosphine Complexes as Catalysts. Ferraris, D.; Young, B.; Dudding, T.; Lectka, T. J. Am. Chem. Soc. 1998, 120, 4548-4549.
- Use of pH-Zone-Refining Countercurrent Chromatography to Separate 2- and 6-Nitro-4-Chloro-Methoxybenzoic Acid. Dudding, T. C.; Mekonnen B.; Ito,Y.; Ziffer, H. J. Liq. Chrom. & Rel. Technol. 1998, 21, 195-201.
- Oxidation of 2-Methoxynaphthlene by Toluene, Naphthalene and Biphenyl Dioxygenases: Structure and Absolute Stereochemistry of Metabolites. Whited, G. M.; Downie, J. C.; Hudlicky, T.; Fearnley, S. P.; Dudding, T. C.; Oliva, H. F.; Parker, D. Bioorganic & Medicinal Chemistry 1994, 2, 727-734.
- Microbial Oxidation of Aromatics in Enantiocontrolled Synthesis. Part 1. Expedient and General Asymmetric Synthesis of Inositols and Carbohydrates via an Unusual Oxidation of a Polarized Diene with Potassium Permanganate. Hudlicky, T.; Mandel, M.; Rouden, J.; Lee, R. S.; Bachmann, B.; Dudding, T. C.; Yost, K. J.; Merols, J. S. J. Chem. Soc., Perkin1 1994, 2, 1553-1567.
- Enantioselective synthesis of mosquito oviposition pheromone and its epimer from a naturally occurring fatty acid. Hurem, D.; Dudding, T. RSC Advances, 2015, 5, 101732-101739.
- Design and synthesis of a chiral seven-membered ring guanidine organocatalyst applied to asymmetric vinylogous aldol reactions.Mirabdolbaghi, R.; Hassan, M.; Dudding, T. Tetrahedron: Asymmetry 2015, 26, 560-566.
- Expanding the Forefront of Strong Organic Bronsted Acids: Proton Catalyzed Hydroamination of Unactivated Alkenes and Activation of Au(I) for Alkyne Hydroamination. Mirabdolbaghi, R.; Dudding, T. Org. Lett. 2015, 17, 1930-1933.
- Mirroring Enzymes: The Role of Hydrogen Bonding in an Asymmetric Organocatalyzed Aza Henry Reaction - a DFT Study. Belding, L.; Taimoory, S. M.; Dudding, T. ACS Catal. 2014, 5, 343-349.
- Shifting the Energy Landscape of Multicomponent Reactions Using Aziridine Aldehyde Dimers: A Mechanistic Study. Belding, L.; Zaretsky, S.; Rotstein, B. H.; Yudin, A. K.; Dudding, T. J. Org. Chem. 2014, 79, 9469-9471.
- Hydroxyproline-Derived Pseudoenantiomeric [2.2.1] Bicyclic Phosphines: Asymmetric Synthesis of (+)- and (-)-Pyrrolines. Henry, C. E.; Xu, Q.; Chio Fan, Y.; Martin, T. J.; Belding, L.; Dudding, T.; Kwon, O. J. Am. Chem. Soc.2014, 136, 11890-11893.
- A Class of Phase-Transfer Catalyst with Interionic Strain: Insight into the Bonding of Disubstituted N- vs Carbene-Stabilized NI-Centered Cations. Mirabdolbaghi, R.; Dudding, T. Org. Lett. 2014, 16, 2790-2793.
- Diastereodivergent total synthesis of mosquitooviposition pheromone. Hurem, D.; Dudding, T. RSC Adv. 2014, 4, 15552-15557.
- A Coordination Compound of Ge0 Stabilized by a Diiminopyridine Ligand. Chu, T.; Belding, L.; van der Est, A.; Dudding, T.; Korobvoc, I.; Nikonov, G. Angew. Chimie Int. Ed. 2014, 53, 2711-2715.
- Synthesis and Theoretical Investigation of a 1,8-Bis(bis(diisopropylamino)cyclopropeniminyl)naphthalene Proton Sponge Derivative. Belding, L.; Dudding, T. Chem. Eur. J. 2014, 20, 1032-1037.
- A Computational Study of the Copper(II)-Catalyzed Enantioselective Intramolecular Aminooxygenation of Alkenes. Belding, L.; Chemler, S. R.; Dudding, T. J. Org. Chem. 2013, 78, 10288–10297.
- A Detailed NMR- and DFT-Based Study of the Sakurai-Hosomi-Yamamoto Asymmetric Allylation Reaction. Hurem, D.; Moiseev, A. G.; Simionescu, R.; Dudding, T. J. Org. Chem. 2013, 78, 4440-4445.
- A synthetic route to chiral C(3)-functionalized phthalides via a Ag(I)-catalyzed allylation/transesterification sequence. Mirabdolbaghi, R.; Dudding, T. Tetrahedron 2013, 69, 3287-3292.
- Reversal of Stereoselectivity in Lithiation of Ferrocenyl-imidazolones: Epimeric Substrates lead to Planar Chiral Enantiomers. Metallinos, C.; John, J.; Nelson, J.; Dudding, T.; Belding, L. Adv. Synth. Catal. 2013, 335, 1211-1219.
- The application of D-Chiro-inositol as a chiral template for the Diels-Alder reaction. Trant, J. F.; Belding, L.; Dudding, T.; Hudlicky, T. Helvetica Chimica Acta. 2012, 95, 2026-2035.
- An Indium-mediated allylative/transesterification DFT-directed approach to chiral C(3)-functionalized phthalides. Mirabdolbaghi, R.; Dudding, T. Org. Lett. 2012, 14, 3748-3751.
- Studies on the ring opening reactions of 3-oxa-1-azabicyclo[3.1.0]hexan-2-ones. Synthesis of aminomethyl oxazolidinones and aziridinyl ureas. Wells, G. M.; Dudding, T.; Belding, L.; Frick, A. J.; Nayek, A.; Huang, J.; Katz, S. J; Bergmeier, S. C. Tetrahedron 2012, 68, 3980-3987.
- Characterization of highly unusual NH-O hydrogen bonding to ester ether oxygen atoms through spectroscopic, kinetic and computational studies. Scerba, M. T.; Deblase, A. F.; Bloom, S.; Dudding, T. C.; Johnson, M. A.; Lectka, T. J. Phys. Chem. A. 2012, 116, 3556-3560.
- A catalytic asymmetric approach to C1-chiral 3-methylene-indan-1-ols. Mirabdolbaghi, R.; Dudding, T. Tetrahedron 2012, 68, 1988-1991.
- Evidence for alkene cis-aminocupration, an aminooxygenation case study: Kinetics, EPR spectroscopy and DFT calculations. Paderes, M. C.; Belding, L.; Fonovic, B.; Dudding, T.; Keister, J. B; Chemler, S. R. Chem. - Eur. J. 2011, 18, 1711-1726.
- Directed ortho,ortho'-dimetalation of hydrobenzoin: Rapid access to hydrobenzoin derivatives useful for asymmetric synthesis. Cho, I.; Meimetis, L.; Belding, L.; M. J. Katz; Dudding, T.; Britton, R. Beilstein J. Org. Chem. 2011, 7, 1315-1322.
- From bifunctional to trifunctional (tricomponent nucleophile-transition metal-Lewis acid) catalysis: The catalytic, enantioselective a-fluorination of acid chlorides. Erb, J.; Paull, D. H.; Dudding, T.; Belding, L.; Lectka, T. J. Am. Chem. Soc. 2011, 133, 7536-7546.
- NHC-catalyzed intramolecular redox amidation for the synthesis of functionalized lactams: Evidence of hydrogen bonding co-catalysis. Thai, K.; Wang, L.; Dudding, T.; Bilodeau, F.; Gravel, M. Org. Lett. 2010, 12, 5708-5711.
- Asymmetric lithiation of boron trifluoride-activated aminoferrocenes: An experimental and computational investigation. Metallinos, C.; Zaifman, J.; Dudding, T.; Van Belle, L.; Taban, K. Adv. Synth. & Catal. 2010, 352, 1967-1982.
- Desymmetrizations forming tetrasubstituted olefins using enantioselective olefin metathesis. Stenne, B.; Timperio, J.; Savoie, J.; Dudding, T.; Collins, S. K. Org. Lett. 2010, 12, 2032-2035.
- The enzymatic cleavage of Si-O bonds: A kinetic analysis of the biocatalyzed hydrolysis of phenyltrimethoxysilane. Frampton, M. B.; Simionescu, R.; Dudding, T.; Zelisko, P. M. J. Molecular Catalysis B: J. Mol. Catal. B: Enzym. 2010, 66, 105-112.
- Incorporation of 2,3-disubstituted-1,4-naphthoquinones into the A1 binding site of photosystem I studied by EPR and ENDOR spectroscopy. van der Est, A.; Pushkar, Y.; Karyagina, I.; Fonovic, B.; Dudding, T.; Niklas, J.; Lubitz, W.; Golbeck, J. H. Appl. Magn. Reson. 2009, 37, 65-83.
- New options for the reactivity of the Burgess reagent with epoxides in both racemic and chiral auxiliary modes structural and mechanistic revisions, computational studies, and application to synthesis. Leisch, H.; Sullivan, B.; Fonovic, B.; Dudding, T.; Hudlicky, T. Eur. J. Org. Chem. 2009, 17, 2806-2819.
- Inverse temperature dependence in the diastereoselective addition of Grignard reagents to a tetrahydrofurfural. Mowat, J.; Kang, B.; Fonovic, B.; Dudding, T.; Britton, R. Org. Lett. 2009, 11, 2057-2060.
- A surprising mechanistic 'switch' in Lewis acid activation: A bifunctional, asymmetric approach to a-hydroxy acid derivatives. Abraham, C. J.; Paull, D. H.; Bekele, T.; Scerba, M. T.; Dudding, T.; Lectka, T. J. Am. Chem. Soc. 2008, 130, 17085-17094.
- Origin of enantioselection in hetero-Diels-Alder reactions catalyzed by naphthyl-TADDOL. Anderson, C. D.; Dudding, T.; Gordillo, R; Houk, K. N. Org. Lett. 2008, 10, 2749-2752.
- Theory-guided design of Bronsted acid-assisted phosphine catalysis: synthesis of dihydropyrones from aldehydes and allenoates. Creech, G.S.; Zhu, X.F.; Fonovic, B.; Dudding, T.; Kwon, O. Tetrahedron 2008, 64, 6935-3942.
- Phosphine triggered [3 + 2] allenoate-acrylate annulation: A mechanistic enlightenment. Mercier, E.; Fonovic, B.; Henry, C.; Kwon, O.; Dudding, T. Tetrahedron Lett. 2007, 48, 3617-3620.
- A mechanistic study on the catalytic, asymmetric α-bromination of acid chlorides. Dogo-Isonagie, C; Bekele, T.; France, S.; Wolfer, S.; Weatherwax, A.; Taggi, A. E.; Paull, D. H.; Dudding, T.; Lectka, T. Eur. J. Org. Chem. 2007, 7, 1091-1100.
- Hydrogen-bonding catalysis induces a change in mechanism of polar Diels-Alder reactions. Gordillo, R; Dudding, T.; Anderson, C. D.; Houk, K. N. Org. Lett. 2007, 9, 501-503.
- An Experimental and theoretical study of the asymmetric lithiation of 1,2,3,5,6,7-hexahydro-3α,4α-diazacyclopenta[def]phenanthren-4-one. Metallinos, C.; Dudding, T.; Zaifman, J.; Chaytor, J. L.; Taylor, N. J. J. Org. Chem. 2007, 72, 957-963.
- Trypsin-catalyzed cross-linking of α,ω;-triethoxysilyl-terminated polydimethylsiloxane: an experimental and computational approach. Zelisko, P. M.; Dudding, T.; Amelien, K. R.; Stanisic, H. Polymer Preprints 2007, 48, 984.
- Theoretical rationale for regioselection in phosphine catalyzed allenoate additions to acrylates, imines and aldehdyes. Dudding, T.; Kwon, O.; Mercier, E. Org. Lett. 2006, 8, 3643-3646.
- Phosphine-Catalyzed Synthesis of 1,3-Dioxan-4-ylidenes. Zhu, X-F; Henry, C. E.; Wang, J.; Dudding, T.; Kwon, O. Org. Lett. 2005, 7, 1387-1390.
- Computational Predictions of Stereochemistry in Asymmetric Thiazolium and Triazolium Catalyzed Benzoin Condensations. Dudding, T.; Houk, K. N. Proc. Natl. Acad. Sci. U.S.A. 2004, 101, 5770-5775.
- A Multistage, One-Pot Procedure Mediated by a Single Catalyst: A New Approach to the Catalytic Asymmetric Synthesis of Alpha-Amino Acids. Hafez, A. M.; Dudding, T.; Wagerle, T. R.; Shah, M. H.; Taggi, A. E.; Lectka, T. J. Org. Chem. 2003, 68, 5819-5825.
- Molecular Mechanics Calculations as Predictors of Enantioselectivity for Chiral Nucleophile Catalyzed Reactions. Taggi, A. E.; Hafez, A. M.; Dudding, T.; Lectka, T. Tetrahedron 2002, 58, 8351-8356.
- A Structure-Activity Study of Spermicidal and anti-HIV properties of Hydroxylated Cationic Surfactants. Wong, Yue Ling; Hubieki, M.; Curfman, C. L.; Doncel, G. F.; Dudding, T. C.; Savle, P. S.; Gandour, R. D. Bioorganic & Medicinal Chemistry 2002, 10, 3599-3608.
- A Catalyst that Plays Multiple Roles: Asymmetric Synthesis of -Substituted Aspartic Acid Derivatives through a Four-Stage, One-Pot Procedure. Dudding, T.; Hafez, A. M.; Taggi, A. E.; Wagerle, T. R.; Lectka, T. Org. Lett. 2002, 4, 387-390.
- Catalytic, Enantioselective Alkylation of -Imino Esters Derivatives. Ferraris, D.; Young, B.; Cox, C.; Dudding, T.; Drury, W.J. III; Ryzhkov, L.; Taggi, A. E.; Lectka, T. J. Am. Chem. Soc. 2002, 124, 67-77.
- Spermicidal, Anti-HIV, and Micellar Properties of Di- and Trihydroxylated Cationic Surfactants. Wong, Yue-Ling; Curfman, C. L.; Doncel, G. F.; Hubieki, M. P.; Dudding, T. C.; Savle, P. S.; Gandour, R. D. Tetrahedron 2002, 58, 45-54.
- Asymmetric Catalysis on Sequentially-linked Columns. Hafez, A. M.; Taggi, A. E.; Dudding, T.; Lectka, T. J. Am. Chem. Soc. 2001, 123, 10853-10859.
- Base- and Acid-catalyzed Interconversions of O-acyl- and N-acyl-ethanolamines: A Cautionary Note for Lipid Analysis. Markey, S. P.; Dudding, T.; Wang, Tao-Chin L. J. Lipid Research 2000, 41, 657-662.
- Catalytic, Enantioselective Alkylation of N,O- and N,N-Acetals and Hemiacetals. Ferraris, D.; Young, B.; Dudding, T.; Drury, W. J. III; Lectka, T. Tetrahedron 1999, 55, 8869-8882.
- Catalytic Enantioselective Alkylation Reactions of N,O-Acetals. Ferraris, D.; Young, B.; Dudding, T.; Drury, W. J. III; Lectka, T. J. Org. Chem. 1999, 64, 2168-2169.
- Diastereo- and Enantioselective Alkylation of Alpha-Imino Esters with Cyclic Enol Silanes Catalyzed by (R)-Tol-BINAP-CuClO4•(MeCN)2. Ferraris, D.; Young, B.; Cox, C.; Drury, W. J. III; Dudding, T.; Lectka, T. J. Org. Chem. 1998, 63, 6090-6091.
- Catalytic, Enantioselective Alkylation of Alpha-Imino Esters Using Late Transition Metal Phosphine Complexes as Catalysts. Ferraris, D.; Young, B.; Dudding, T.; Lectka, T. J. Am. Chem. Soc. 1998, 120, 4548-4549.
- Use of pH-Zone-Refining Countercurrent Chromatography to Separate 2- and 6-Nitro-4-Chloro-Methoxybenzoic Acid. Dudding, T. C.; Mekonnen B.; Ito,Y.; Ziffer, H. J. Liq. Chrom. & Rel. Technol. 1998, 21, 195-201.
- Oxidation of 2-Methoxynaphthlene by Toluene, Naphthalene and Biphenyl Dioxygenases: Structure and Absolute Stereochemistry of Metabolites. Whited, G. M.; Downie, J. C.; Hudlicky, T.; Fearnley, S. P.; Dudding, T. C.; Oliva, H. F.; Parker, D. Bioorganic & Medicinal Chemistry 1994, 2, 727-734.
- Microbial Oxidation of Aromatics in Enantiocontrolled Synthesis. Part 1. Expedient and General Asymmetric Synthesis of Inositols and Carbohydrates via an Unusual Oxidation of a Polarized Diene with Potassium Permanganate. Hudlicky, T.; Mandel, M.; Rouden, J.; Lee, R. S.; Bachmann, B.; Dudding, T. C.; Yost, K. J.; Merols, J. S. J. Chem. Soc., Perkin1 1994, 2, 1553-1567.
