| Year |
Citation |
Score |
| 2024 |
Garrison NG, Holt E, Wang M, Rowshanpour R, Kiame N, Lam W, Borukhova F, Dudding T, Lectka T. Complementary Tandem Reaction Manifolds and "Switch Mechanisms" in the Reaction of Epoxides with Selectfluor. The Journal of Organic Chemistry. PMID 39356244 DOI: 10.1021/acs.joc.4c01470 |
0.628 |
|
| 2023 |
Ruskin J, Sachs RK, Wang M, Dekeyser R, Lew Z, Williams P, Hwang H, Majumdar A, Dudding T, Lectka T. Metal Ion-Induced Large Fragment Deactivation: A Different Strategy for Site-Selectivity in a Complex Molecule. Angewandte Chemie (International Ed. in English). e202317070. PMID 38063469 DOI: 10.1002/anie.202317070 |
0.585 |
|
| 2023 |
Holt E, Ruskin J, Garrison NG, Vemulapalli S, Lam W, Kiame N, Henriquez N, Borukhova F, Williams J, Dudding T, Lectka T. Photoactivated Pyridine Directed Fluorination through Hydrogen Atom Transfer. The Journal of Organic Chemistry. PMID 38033293 DOI: 10.1021/acs.joc.3c02146 |
0.568 |
|
| 2023 |
Wang M, Rowshanpour R, Guan L, Ruskin J, Nguyen PM, Wang Y, Zhang QA, Liu R, Ling B, Woltornist R, Stephens AM, Prasad A, Dudding T, Lectka T, Pitts CR. Competition between C-C and C-H Bond Fluorination: A Continuum of Electron Transfer and Hydrogen Atom Transfer Mechanisms. Journal of the American Chemical Society. 145: 22442-22455. PMID 37791901 DOI: 10.1021/jacs.3c06477 |
0.802 |
|
| 2023 |
Kazim M, Wang M, Vemulapalli S, Nguyen PM, Wang Y, Siegler MA, Dudding T, Lectka T. How Do Face-to-Face Stacked Aromatic Rings Activate Each Other to Electrophilic Aromatic Substitution? Organic Letters. PMID 37279142 DOI: 10.1021/acs.orglett.3c01401 |
0.549 |
|
| 2023 |
Kazim M, Feng Z, Vemulapalli S, Siegler MA, Chopra A, Nguyen PM, Holl MG, Guan L, Dudding T, Tantillo DJ, Lectka T. Through-Space, Lone-Pair Promoted Aromatic Substitution: A Relay Mechanism Can Beat Out Direct Activation. Chemistry (Weinheim An Der Bergstrasse, Germany). e202301550. PMID 37219499 DOI: 10.1002/chem.202301550 |
0.806 |
|
| 2023 |
Holt E, Garrison NG, Rowshanpour R, Kim JJ, Henriquez N, Lam W, Kiame N, Williams J, Zhao S, Dudding T, Lectka T. C-C Bond Activation and Demethylenation of Epoxides by Amine Radical Dications. The Journal of Organic Chemistry. PMID 37159569 DOI: 10.1021/acs.joc.3c00605 |
0.594 |
|
| 2022 |
Harry SA, Vemulapalli S, Dudding T, Lectka T. Rational Computational Design of Systems Exhibiting Strong Halogen Bonding Involving Fluorine in Bicyclic Diamine Derivatives. The Journal of Organic Chemistry. 87: 8413-8419. PMID 35658438 DOI: 10.1021/acs.joc.2c00497 |
0.546 |
|
| 2022 |
Capilato JN, Harry SA, Siegler MA, Lectka T. Spectroscopic and Crystallographic Characterization of the R N -C-H⋅⋅⋅X Interaction. Chemistry (Weinheim An Der Bergstrasse, Germany). 28: e202103922. PMID 35133051 DOI: 10.1002/chem.202103922 |
0.783 |
|
| 2021 |
Dehnen S, Schafer LL, Lectka T, Togni A. Fluorine: A Very Special Element and Its Very Special Impacts on Chemistry. The Journal of Organic Chemistry. 86: 16213-16219. PMID 34806389 DOI: 10.1021/acs.joc.1c02745 |
0.399 |
|
| 2021 |
Dehnen S, Schafer LL, Lectka T, Togni A. Fluorine: A Very Special Element and Its Very Special Impacts on Chemistry. Organic Letters. 23: 9013-9019. PMID 34806386 DOI: 10.1021/acs.orglett.1c03799 |
0.399 |
|
| 2021 |
Dehnen S, Schafer LL, Lectka T, Togni A. Fluorine: A Very Special Element and Its Very Special Impacts on Chemistry. Inorganic Chemistry. 60: 17419-17425. PMID 34806365 DOI: 10.1021/acs.inorgchem.1c03509 |
0.399 |
|
| 2021 |
Hoffmann KF, Wiesner A, Müller C, Steinhauer S, Beckers H, Kazim M, Pitts CR, Lectka T, Riedel S. Structural proof of a [C-F-C] fluoronium cation. Nature Communications. 12: 5275. PMID 34489464 DOI: 10.1038/s41467-021-25592-6 |
0.653 |
|
| 2021 |
Capilato JN, Lectka T. Arene Amination Instead of Fluorination: Substitution Pattern Governs the Reactivity of Dialkoxybenzenes with Selectfluor. The Journal of Organic Chemistry. 86: 5771-5777. PMID 33787260 DOI: 10.1021/acs.joc.1c00231 |
0.806 |
|
| 2020 |
Capilato JN, Siegler MA, Rowshanpour R, Dudding T, Lectka T. Cooperative Noncovalent Interactions Lead to a Highly Diastereoselective Sulfonyl-Directed Fluorination of Steroidal α,β-Unsaturated Hydrazones. The Journal of Organic Chemistry. PMID 33300794 DOI: 10.1021/acs.joc.0c02716 |
0.801 |
|
| 2020 |
Ghorbani F, Harry SA, Capilato JN, Pitts CR, Joram J, Peters GN, Tovar JD, Smajlagic I, Siegler MA, Dudding T, Lectka T. Carbonyl-Directed Aliphatic Fluorination: A Special Type of Hydrogen Atom Transfer Beats Out Norrish II. Journal of the American Chemical Society. PMID 32786786 DOI: 10.1021/Jacs.0C07004 |
0.792 |
|
| 2020 |
Smajlagic I, Kazim M, Lectka T, Dudding T. DFT Case Study of the Mechanism of a Metal-Free Oxygen Atom Insertion into a -Quinone Methide C(sp)-C(sp) Bond. The Journal of Organic Chemistry. PMID 32633515 DOI: 10.1021/Acs.Joc.0C01371 |
0.788 |
|
| 2020 |
Kazim M, Guan L, Chopra A, Sun R, Siegler MA, Lectka T. Switching a HO···π Interaction to a Nonconventional OH···π Hydrogen Bond: A Completed Crystallographic Puzzle. The Journal of Organic Chemistry. PMID 32633510 DOI: 10.1021/Acs.Joc.0C01121 |
0.792 |
|
| 2020 |
Kazim M, Siegler MA, Lectka T. Close Amide NH···F Hydrogen Bonding Interactions in 1,8-Disubstituted Naphthalenes. The Journal of Organic Chemistry. PMID 32227992 DOI: 10.1021/Acs.Joc.0C00553 |
0.32 |
|
| 2020 |
Capilato JN, Pitts CR, Rowshanpour R, Dudding T, Lectka T. Site-Selective Photochemical Fluorination of Ketals: Unanticipated Outcomes in Selectivity and Stability. The Journal of Organic Chemistry. PMID 32031800 DOI: 10.1021/Acs.Joc.9B03047 |
0.816 |
|
| 2019 |
Holl MG, Pitts CR, Lectka T. Quest for a Symmetric [C-F-C] Fluoronium Ion in Solution: A Winding Path to Ultimate Success. Accounts of Chemical Research. PMID 31877026 DOI: 10.1021/Acs.Accounts.9B00554 |
0.68 |
|
| 2019 |
Capilato JN, Bume DD, Lee WH, Hoffenberg LES, Jokhai RT, Lectka T. Correction to Fluorofunctionalization of C═C Bonds with Selectfluor: Synthesis of β-Fluoropiperazines through a Substrate-Guided Reactivity Switch. The Journal of Organic Chemistry. PMID 31718185 DOI: 10.1021/acs.joc.9b02989 |
0.792 |
|
| 2019 |
Kazim M, Foy H, Siegler MA, Dudding T, Lectka T. Discovery and Mechanistic Study of a Totally Organic C-C Oxygen Insertion Reaction. The Journal of Organic Chemistry. PMID 31577426 DOI: 10.1021/Acs.Joc.9B02238 |
0.631 |
|
| 2019 |
Liu G, Ciborowski SM, Pitts CR, Graham JD, Buytendyk AM, Lectka T, Bowen KH. Observation of the dipole- and quadrupole-bound anions of 1,4-dicyanocyclohexane. Physical Chemistry Chemical Physics : Pccp. PMID 31397463 DOI: 10.1039/C9Cp04010B |
0.657 |
|
| 2019 |
Young JD, Honick CR, Zhou J, Pitts CR, Ghorbani F, Peters GM, Lectka T, Tovar JD, Bragg AE. Energy- and conformer-dependent excited-state relaxation of an E/Z photoswitchable thienyl-ethene. Physical Chemistry Chemical Physics : Pccp. PMID 30920561 DOI: 10.1039/C9Cp01226E |
0.654 |
|
| 2019 |
Kazim M, Siegler MA, Lectka T. A Case of Serendipity: Synthesis, Characterization, and Unique Chemistry of a Stable, Ring-Unsubstituted Aliphatic p-Quinone Methide. Organic Letters. PMID 30859826 DOI: 10.1021/Acs.Orglett.9B00615 |
0.394 |
|
| 2019 |
York GD, Siegler MA, Patel DD, Lectka T. Synthesis and X-Ray crystallography of a substituted trityl fluoride: Ordering power of a C-F bond Journal of Fluorine Chemistry. 228: 109377. DOI: 10.1016/J.Jfluchem.2019.109377 |
0.305 |
|
| 2018 |
Capilato JN, Bume DD, Lee WH, Hoffenberg LES, Jokhai RT, Lectka T. Fluorofunctionalization of C═C Bonds with Selectfluor: Synthesis of β-Fluoropiperazines through a Substrate-Guided Reactivity Switch. The Journal of Organic Chemistry. PMID 30418026 DOI: 10.1021/Acs.Joc.8B02429 |
0.826 |
|
| 2018 |
Bume DD, Harry SA, Lectka T, Pitts CR. Catalyzed and Promoted Aliphatic Fluorination. The Journal of Organic Chemistry. PMID 29894188 DOI: 10.1021/Acs.Joc.8B00982 |
0.711 |
|
| 2018 |
Pitts CR, Holl MG, Lectka T. Spectroscopic Characterization of a [C-F-C]+ Fluoronium Ion in Solution. Angewandte Chemie (International Ed. in English). PMID 29316122 DOI: 10.1002/Anie.201712021 |
0.665 |
|
| 2018 |
Bume DD, Harry SA, Pitts CR, Lectka T. Sensitized Aliphatic Fluorination Directed by Terpenoidal Enones: A "Visible Light" Approach. The Journal of Organic Chemistry. PMID 29293338 DOI: 10.1021/Acs.Joc.7B02807 |
0.678 |
|
| 2018 |
Holl MG, Pitts CR, Lectka T. Fluor in einer C-F-Bindung als Schlüssel für die Käfigbildung Angewandte Chemie. 130: 2806-2815. DOI: 10.1002/Ange.201710423 |
0.639 |
|
| 2017 |
Bume DD, Pitts CR, Ghorbani F, Harry SA, Capilato JN, Siegler MA, Lectka T. Ketones as directing groups in photocatalytic sp(3) C-H fluorination. Chemical Science. 8: 6918-6923. PMID 29147517 DOI: 10.1039/C7Sc02703F |
0.806 |
|
| 2017 |
Holl MG, Pitts CR, Lectka T. Fluorine in a C-F Bond as the Key to Cage Formation. Angewandte Chemie (International Ed. in English). PMID 29141116 DOI: 10.1002/Anie.201710423 |
0.677 |
|
| 2017 |
Guan L, Holl MG, Pitts CR, Struble MD, Siegler MA, Lectka T. Through-space Activation can Override Substituent Effects in Electrophilic Aromatic Substitution. Journal of the American Chemical Society. PMID 28992687 DOI: 10.1021/Jacs.7B09792 |
0.8 |
|
| 2017 |
Pitts CR, Siegler MA, Lectka T. An Intermolecular Aliphatic C-F---H-C Interaction in the Presence of "Stronger" Hydrogen Bond Acceptors: Crystallographic, Computational, and IR Studies. The Journal of Organic Chemistry. PMID 28240908 DOI: 10.1021/Acs.Joc.7B00268 |
0.677 |
|
| 2017 |
Pitts CR, Bume DD, Harry SA, Siegler MA, Lectka T. Multiple Enone-Directed Reactivity Modes Lead to the Selective Photochemical Fluorination of Polycyclic Terpenoid Derivatives. Journal of the American Chemical Society. PMID 28146358 DOI: 10.1021/Jacs.7B00335 |
0.702 |
|
| 2016 |
Struble MD, Guan L, Siegler MA, Lectka T. A C-F Bond Directed Diels-Alder Reaction. The Journal of Organic Chemistry. PMID 27467448 DOI: 10.1021/Acs.Joc.6B01489 |
0.801 |
|
| 2016 |
Holl MG, Struble MD, Singal P, Siegler MA, Lectka T. Positioning a Carbon-Fluorine Bond over the π Cloud of an Aromatic Ring: A Different Type of Arene Activation. Angewandte Chemie (International Ed. in English). PMID 27145463 DOI: 10.1002/Anie.201601989 |
0.41 |
|
| 2016 |
Pitts CR, Ling B, Snyder JA, Bragg AE, Lectka T. Aminofluorination of Cyclopropanes: A Multifold Approach through a Common, Catalytically Generated Intermediate. Journal of the American Chemical Society. PMID 27136383 DOI: 10.1021/Jacs.6B02838 |
0.71 |
|
| 2016 |
Bume DD, Pitts CR, Jokhai RT, Lectka T. Direct, visible light-sensitized benzylic C H fluorination of peptides using dibenzosuberenone: selectivity for phenylalanine-like residues Tetrahedron. 72: 6031-6036. DOI: 10.1016/J.Tet.2016.08.018 |
0.688 |
|
| 2016 |
Holl MG, Struble MD, Siegler MA, Lectka T. The close interaction of a C F bond with a carbonyl π–system: Attractive, repulsive, or both? Journal of Fluorine Chemistry. 188: 126-130. DOI: 10.1016/J.Jfluchem.2016.06.016 |
0.328 |
|
| 2016 |
Bume DD, Pitts CR, Lectka T. Tandem C-C Bond Cleavage of Cyclopropanols and Oxidative Aromatization by Manganese(IV) Oxide in a Direct C-H to C-C Functionalization of Heteroaromatics European Journal of Organic Chemistry. 2016: 26-30. DOI: 10.1002/Ejoc.201501405 |
0.705 |
|
| 2016 |
Bume DD, Pitts CR, Lectka T. ChemInform Abstract: Tandem C-C Bond Cleavage of Cyclopropanols and Oxidative Aromatization by Manganese(IV) Oxide in a Direct C-H to C-C Functionalization of Heteroaromatics. Cheminform. 47. DOI: 10.1002/CHIN.201621044 |
0.637 |
|
| 2015 |
Pitts CR, Bloom MS, Bume DD, Zhang QA, Lectka T. Unstrained C-C bond activation and directed fluorination through photocatalytically-generated radical cations. Chemical Science. 6: 5225-5229. PMID 29449927 DOI: 10.1039/C5Sc01973G |
0.725 |
|
| 2015 |
Keolopile ZG, Gutowski M, Buonaugurio AM, Collins E, Zhang X, Erb JM, Lectka T, Bowen KH, Allan M. On the Importance of Time Scale and Local Environment in Electron-Driven Proton Transfer. The Anion of Acetoacetic Acid. Journal of the American Chemical Society. PMID 26486969 DOI: 10.1021/Jacs.5B08134 |
0.607 |
|
| 2015 |
Struble MD, Holl MG, Scerba MT, Siegler MA, Lectka T. Search for a Symmetrical C-F-C Fluoronium Ion in Solution: Kinetic Isotope Effects, Synthetic Labeling, and Computational, Solvent, and Rate Studies. Journal of the American Chemical Society. 137: 11476-90. PMID 26275357 DOI: 10.1021/Jacs.5B07066 |
0.72 |
|
| 2015 |
Bloom S, Bume DD, Pitts CR, Lectka T. Site-Selective Approach to β-Fluorination: Photocatalyzed Ring Opening of Cyclopropanols. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 8060-3. PMID 25877004 DOI: 10.1002/Chem.201501081 |
0.798 |
|
| 2015 |
Pitts CR, Bloom MS, Bume DD, Zhang QA, Lectka T. Unstrained C-C bond activation and directed fluorination through photocatalytically-generated radical cations Chemical Science. 6: 5225-5229. DOI: 10.1039/c5sc01973g |
0.65 |
|
| 2014 |
Bloom S, McCann M, Lectka T. Photocatalyzed benzylic fluorination: shedding "light" on the involvement of electron transfer. Organic Letters. 16: 6338-41. PMID 25493423 DOI: 10.1021/Ol503094M |
0.637 |
|
| 2014 |
Griswold A, Bloom S, Lectka T. A chelating nucleophile plays a starring role: 1,8-naphthyridine-catalyzed polycomponent α,α-difluorination of acid chlorides. The Journal of Organic Chemistry. 79: 9830-4. PMID 25222052 DOI: 10.1021/Jo501534K |
0.668 |
|
| 2014 |
Pitts CR, Ling B, Woltornist R, Liu R, Lectka T. Triethylborane-initiated radical chain fluorination: a synthetic method derived from mechanistic insight. The Journal of Organic Chemistry. 79: 8895-9. PMID 25137438 DOI: 10.1021/Jo501520E |
0.682 |
|
| 2014 |
Struble MD, Kelly C, Siegler MA, Lectka T. Search for a strong, virtually "no-shift" hydrogen bond: a cage molecule with an exceptional OH⋅⋅⋅F interaction. Angewandte Chemie (International Ed. in English). 53: 8924-8. PMID 24989940 DOI: 10.1002/Anie.201403599 |
0.308 |
|
| 2014 |
Pitts CR, Bloom S, Woltornist R, Auvenshine DJ, Ryzhkov LR, Siegler MA, Lectka T. Direct, catalytic monofluorination of sp³ C-H bonds: a radical-based mechanism with ionic selectivity. Journal of the American Chemical Society. 136: 9780-91. PMID 24943675 DOI: 10.1021/Ja505136J |
0.788 |
|
| 2014 |
Pitts CR, Lectka T. Chemical synthesis of β-lactams: asymmetric catalysis and other recent advances. Chemical Reviews. 114: 7930-53. PMID 24555548 DOI: 10.1021/Cr4005549 |
0.702 |
|
| 2014 |
Bloom S, Knippel JL, Lectka T. A photocatalyzed aliphatic fluorination Chemical Science. 5: 1175-1178. DOI: 10.1039/C3Sc53261E |
0.687 |
|
| 2014 |
Bloom S, Knippel JL, Holl MG, Barber R, Lectka T. A cooperative allylic fluorination: Combination of nucleophilic and electrophilic fluorine sources Tetrahedron Letters. 55: 4576-4580. DOI: 10.1016/J.Tetlet.2014.05.093 |
0.702 |
|
| 2013 |
Bloom S, Sharber SA, Holl MG, Knippel JL, Lectka T. Metal-catalyzed benzylic fluorination as a synthetic equivalent to 1,4-conjugate addition of fluoride. The Journal of Organic Chemistry. 78: 11082-6. PMID 24073747 DOI: 10.1021/Jo401796G |
0.67 |
|
| 2013 |
DeBlase AF, Bloom S, Lectka T, Jordan KD, McCoy AB, Johnson MA. Origin of the diffuse vibrational signature of a cyclic intramolecular proton bond: Anharmonic analysis of protonated 1,8-disubstituted naphthalene ions. The Journal of Chemical Physics. 139: 024301. PMID 23862937 DOI: 10.1063/1.4810878 |
0.614 |
|
| 2013 |
Struble MD, Scerba MT, Siegler M, Lectka T. Evidence for a symmetrical fluoronium ion in solution. Science (New York, N.Y.). 340: 57-60. PMID 23559245 DOI: 10.1126/Science.1231247 |
0.698 |
|
| 2013 |
Bloom S, Pitts CR, Woltornist R, Griswold A, Holl MG, Lectka T. Iron(II)-catalyzed benzylic fluorination. Organic Letters. 15: 1722-4. PMID 23527764 DOI: 10.1021/Ol400424S |
0.792 |
|
| 2013 |
Deblase AF, Scerba MT, Lectka T, Johnson MA. Vibrational predissociation spectroscopy of Ar-tagged, trisubstituted silyl cations Chemical Physics Letters. 568: 9-13. DOI: 10.1016/J.Cplett.2013.03.002 |
0.673 |
|
| 2012 |
Bloom S, Pitts CR, Miller DC, Haselton N, Holl MG, Urheim E, Lectka T. A polycomponent metal-catalyzed aliphatic, allylic, and benzylic fluorination. Angewandte Chemie (International Ed. in English). 51: 10580-3. PMID 22976771 DOI: 10.1002/Anie.201203642 |
0.811 |
|
| 2012 |
Erb J, Strull J, Miller D, He J, Lectka T. The Diels-Alder cyclization of ketenimines. Organic Letters. 14: 2191-3. PMID 22480176 DOI: 10.1021/Ol300742T |
0.687 |
|
| 2012 |
Scerba MT, DeBlase AF, Bloom S, Dudding T, Johnson MA, Lectka T. Characterization of highly unusual NH+-O hydrogen bonding to ester ether oxygen atoms through spectroscopic and computational studies. The Journal of Physical Chemistry. A. 116: 3556-60. PMID 22394264 DOI: 10.1021/Jp211688V |
0.791 |
|
| 2012 |
Scerba MT, Bloom S, Haselton N, Siegler M, Jaffe J, Lectka T. Interaction of a C-F bond with the π-system of a C═C bond or "head on" with a proximate C-H bond. The Journal of Organic Chemistry. 77: 1605-9. PMID 22283798 DOI: 10.1021/Jo2024152 |
0.776 |
|
| 2012 |
Bloom S, Scerba MT, Erb J, Lectka T. ChemInform Abstract: Tricomponent Catalytic α,α-Difluorination of Acid Chlorides. Cheminform. 43: no-no. DOI: 10.1002/chin.201206057 |
0.782 |
|
| 2011 |
Scerba MT, Leavitt CM, Diener ME, DeBlase AF, Guasco TL, Siegler MA, Bair N, Johnson MA, Lectka T. NH+-F hydrogen bonding in a fluorinated "proton sponge" derivative: integration of solution, solid-state, gas-phase, and computational studies. The Journal of Organic Chemistry. 76: 7975-84. PMID 21888333 DOI: 10.1021/Jo2015328 |
0.705 |
|
| 2011 |
Bloom S, Scerba MT, Erb J, Lectka T. Tricomponent catalytic α,α-difluorination of acid chlorides. Organic Letters. 13: 5068-71. PMID 21875036 DOI: 10.1021/Ol2019295 |
0.819 |
|
| 2011 |
Erb J, Paull DH, Dudding T, Belding L, Lectka T. From bifunctional to trifunctional (tricomponent nucleophile-transition metal-lewis acid) catalysis: the catalytic, enantioselective α-fluorination of acid chlorides. Journal of the American Chemical Society. 133: 7536-46. PMID 21513338 DOI: 10.1021/Ja2014345 |
0.838 |
|
| 2010 |
Erb J, Alden-Danforth E, Kopf N, Scerba MT, Lectka T. Combining asymmetric catalysis with natural product functionalization through enantioselective alpha-fluorination. The Journal of Organic Chemistry. 75: 969-71. PMID 20039641 DOI: 10.1021/Jo9024072 |
0.811 |
|
| 2010 |
France S, Wack H, Hafez AM, Taggi AE, Witsil DR, Lectka T. ChemInform Abstract: Bifunctional Asymmetric Catalysis: A Tandem Nucleophile/Lewis Acid Promoted Synthesis of β-Lactams. Cheminform. 33: no-no. DOI: 10.1002/chin.200238091 |
0.755 |
|
| 2010 |
Ferraris D, Young B, Cox C, Dudding T, Drury III WJ, Ryzhkov L, Taggi AE, Lectka T. ChemInform Abstract: Catalytic, Enantioselective Alkylation of α-Imino Esters: The Synthesis of Nonnatural α-Amino Acid Derivatives. Cheminform. 33: no-no. DOI: 10.1002/chin.200224036 |
0.651 |
|
| 2010 |
Wack H, Taggi AE, Hafez AM, Drury III WJ, Lectka T. ChemInform Abstract: Catalytic, Asymmetric α-Halogenation. Cheminform. 32: no-no. DOI: 10.1002/chin.200124065 |
0.729 |
|
| 2010 |
Evans DA, Barnes DM, Johnson JS, Lectka T, von Matt P, Miller SJ, Murry JA, Norcross RD, Shaughnessy EA, Campos KR. ChemInform Abstract: Bis(oxazoline) and Bis(oxazolinyl)pyridine Copper Complexes as Enantioselective Diels-Alder Catalysts: Reaction Scope and Synthetic Applications. Cheminform. 30: no-no. DOI: 10.1002/chin.199952044 |
0.614 |
|
| 2010 |
Evans DA, Miller SJ, Lectka T, von Matt P. ChemInform Abstract: Chiral Bis(oxazoline)copper(II) Complexes as Lewis Acid Catalysts for the Enantioselective Diels-Alder Reaction. Cheminform. 30: no-no. DOI: 10.1002/chin.199952043 |
0.493 |
|
| 2010 |
FERRARIS D, YOUNG B, COX C, DRURY WJI, DUDDING T, LECTKA T. ChemInform Abstract: Diastereo- and Enantioselective Alkylation of α-Imino Esters with Enol Silanes Catalyzed by (R)-Tol-BINAP-CuClO4×(MeCN)2. Cheminform. 30: no-no. DOI: 10.1002/chin.199907209 |
0.617 |
|
| 2010 |
EVANS DA, LECTKA T, MILLER SJ. ChemInform Abstract: Bis(imine)-Copper(II) Complexes as Chiral Lewis Acid Catalysts for the Diels-Alder Reaction. Cheminform. 25: no-no. DOI: 10.1002/chin.199404060 |
0.488 |
|
| 2010 |
EVANS DA, MILLER SJ, LECTKA T. ChemInform Abstract: Bis(oxazoline)copper(II) Complexes as Chiral Catalysts for the Enantioselective Diels-Alder Reaction. Cheminform. 24: no-no. DOI: 10.1002/chin.199348065 |
0.461 |
|
| 2009 |
Paull DH, Weatherwax A, Lectka T. Catalytic, asymmetric reactions of ketenes and ketene enolates. Tetrahedron. 65: 3771-6803. PMID 21494417 DOI: 10.1016/J.Tet.2009.05.079 |
0.813 |
|
| 2009 |
Abraham CJ, Paull DH, Dogo-Isonagie C, Lectka T. Diastereoselective Synthesis of trans-beta-Lactams Using a Simple Multifunctional Catalyst. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 10: 1651-1654. PMID 20442797 DOI: 10.1055/S-0029-1217348 |
0.827 |
|
| 2009 |
Lectka T, Paull D, Scerba M, Alden-Danforth E, Widger L. α-Fluorination of Acid Chlorides Synfacts. 2009: 0291-0291. DOI: 10.1055/S-0028-1087785 |
0.793 |
|
| 2009 |
Li X, Grubisic A, Eustis S, Wang D, Lectka T, Ganteför GF, Bowen KH, Burgert R, Schnöckel H. The reaction of aluminum cluster anions with tetrakis(dimethylamino)ethylene (TDMAE): Insertion of an aluminum anion into a C-N bond Chemical Physics Letters. 481: 190-193. DOI: 10.1016/J.Cplett.2009.09.101 |
0.304 |
|
| 2009 |
Abraham CJ, Paull DH, Dogo-Isonagie C, Lectka T. ChemInform Abstract: Diastereoselective Synthesis of trans-β-Lactams Using a Simple Multifunctional Catalyst. Cheminform. 40. DOI: 10.1002/chin.200944111 |
0.813 |
|
| 2009 |
Paull DH, Scerba MT, Alden-Danforth E, Widger LR, Lectka T. ChemInform Abstract: Catalytic, Asymmetric α-Fluorination of Acid Chlorides: Dual Metal-Ketene Enolate Activation. Cheminform. 40. DOI: 10.1002/chin.200920034 |
0.81 |
|
| 2008 |
Abraham CJ, Paull DH, Bekele T, Scerba MT, Dudding T, Lectka T. A surprising mechanistic "switch" in Lewis acid activation: a bifunctional, asymmetric approach to alpha-hydroxy acid derivatives. Journal of the American Chemical Society. 130: 17085-94. PMID 19053448 DOI: 10.1021/Ja806818A |
0.837 |
|
| 2008 |
Paull DH, Scerba MT, Alden-Danforth E, Widger LR, Lectka T. Catalytic, asymmetric alpha-fluorination of acid chlorides: dual metal-ketene enolate activation. Journal of the American Chemical Society. 130: 17260-1. PMID 19049284 DOI: 10.1021/Ja807792C |
0.826 |
|
| 2008 |
Alden-Danforth E, Scerba MT, Lectka T. Asymmetric cycloadditions of o-quinone methides employing chiral ammonium fluoride precatalysts. Organic Letters. 10: 4951-3. PMID 18850717 DOI: 10.1021/Ol802029E |
0.838 |
|
| 2008 |
Paull DH, Abraham CJ, Scerba MT, Alden-Danforth E, Lectka T. Bifunctional asymmetric catalysis: cooperative Lewis acid/base systems. Accounts of Chemical Research. 41: 655-63. PMID 18402470 DOI: 10.1021/Ar700261A |
0.83 |
|
| 2007 |
Paull DH, Alden-Danforth E, Wolfer J, Dogo-Isonagie C, Abraham CJ, Lectka T. An Asymmetric, bifunctional catalytic approach to non-natural alpha-amino acid derivatives. The Journal of Organic Chemistry. 72: 5380-2. PMID 17555354 DOI: 10.1021/Jo070472X |
0.832 |
|
| 2007 |
Paull DH, Wolfer J, Grebinski JW, Weatherwax A, Lectka T. Catalytic, asymmetric inverse electron demand hetero diels-alder reactions of o-benzoquinone derivatives and ketene enolates Chimia. 61: 240-246. DOI: 10.2533/Chimia.2007.240 |
0.835 |
|
| 2007 |
Lectka T, Abraham C, Paull D, Scerba M, Grebinski J. Bifunctional Inverse Electron Demand Hetero-Diels-Alder Reactions Synfacts. 2007: 0072-0072. DOI: 10.1055/S-2006-955718 |
0.794 |
|
| 2007 |
Lectka T, Wolfer J, Bekele T, Abraham C, Dogo-Isonagie C. Highly Enantioselective Synthesis of 1,4-Benzoxazinones and α-Amino Acids Synfacts. 2007: 0092-0092. DOI: 10.1055/S-2006-955660 |
0.755 |
|
| 2007 |
Dogo-Isonagie C, Bekele T, France S, Wolfer J, Weatherwax A, Taggi AE, Paull DH, Dudding T, Lectka T. A mechanistic study on the catalytic, asymmetric α-bromination of acid chlorides European Journal of Organic Chemistry. 1091-1100. DOI: 10.1002/Ejoc.200600819 |
0.808 |
|
| 2006 |
Dogo-Isonagie C, Bekele T, France S, Wolfer J, Weatherwax A, Taggi AE, Lectka T. Scalable methodology for the catalytic, asymmetric alpha-bromination of acid chlorides. The Journal of Organic Chemistry. 71: 8946-9. PMID 17081026 DOI: 10.1021/Jo061522L |
0.82 |
|
| 2006 |
Wolfer J, Bekele T, Abraham CJ, Dogo-Isonagie C, Lectka T. Catalytic, asymmetric synthesis of 1,4-benzoxazinones: a remarkably enantioselective route to alpha-amino acid derivatives from o-benzoquinone imides. Angewandte Chemie (International Ed. in English). 45: 7398-400. PMID 17036371 DOI: 10.1002/Anie.200602801 |
0.822 |
|
| 2006 |
Abraham CJ, Paull DH, Scerba MT, Grebinski JW, Lectka T. Catalytic, enantioselective bifunctional inverse electron demand hetero-Diels-Alder reactions of ketene enolates and o-benzoquinone diimides. Journal of the American Chemical Society. 128: 13370-1. PMID 17031945 DOI: 10.1021/Ja065754D |
0.83 |
|
| 2006 |
Bekele T, Shah MH, Wolfer J, Abraham CJ, Weatherwax A, Lectka T. Catalytic, enantioselective [4 + 2]-cycloadditions of ketene enolates and o-quinones: efficient entry to chiral, alpha-oxygenated carboxylic acid derivatives. Journal of the American Chemical Society. 128: 1810-1. PMID 16464078 DOI: 10.1021/Ja058077G |
0.838 |
|
| 2006 |
Bekele T, Shah MH, Wolfer J, Abraham CJ, Weatherwax A, Lectka T. Enantioselective [4+2] Cycloadditions of Ketenes with o-Quinones Synfacts. 2006: 387-387. DOI: 10.1055/S-2006-932102 |
0.705 |
|
| 2006 |
Lectka T. Stereoselective and catalyzed halogenation reactions Tetrahedron. 62: 7149. DOI: 10.1016/j.tet.2006.05.035 |
0.314 |
|
| 2005 |
Weatherwax A, Abraham CJ, Lectka T. An anionic nucleophilic catalyst system for the diastereoselective synthesis of trans-beta-lactams. Organic Letters. 7: 3461-3. PMID 16048317 DOI: 10.1021/Ol0511070 |
0.823 |
|
| 2005 |
France S, Bernstein D, Weatherwax A, Lectka T. Performing the synthesis of a complex molecule on sequentially linked columns: toward the development of a "synthesis machine". Organic Letters. 7: 3009-12. PMID 15987192 DOI: 10.1021/Ol050980Y |
0.783 |
|
| 2005 |
France S, Shah MH, Weatherwax A, Wack H, Roth JP, Lectka T. Bifunctional Lewis acid-nucleophile-based asymmetric catalysis: mechanistic evidence for imine activation working in tandem with chiral enolate formation in the synthesis of beta-lactams. Journal of the American Chemical Society. 127: 1206-15. PMID 15669860 DOI: 10.1021/Ja044179F |
0.831 |
|
| 2005 |
Bernstein D, France S, Wolfer J, Lectka T. A column-based 'flush and flow' system for the asymmetric α-chlorination of acid halides Tetrahedron Asymmetry. 16: 3481-3483. DOI: 10.1016/J.Tetasy.2005.09.014 |
0.815 |
|
| 2005 |
France S, Weatherwax A, Lectka T. Recent developments in catalytic, asymmetric α-halogenation: A new frontier in asymmetric catalysis European Journal of Organic Chemistry. 475-479. DOI: 10.1002/Ejoc.200400517 |
0.697 |
|
| 2004 |
France S, Weatherwax A, Taggi AE, Lectka T. Advances in the catalytic, asymmetric synthesis of beta-lactams. Accounts of Chemical Research. 37: 592-600. PMID 15311958 DOI: 10.1021/Ar030055G |
0.804 |
|
| 2004 |
Wack H, France S, Hafez AM, Drury WJ, Weatherwax A, Lectka T. Development of a new dimeric cyclophane ligand: application to enhanced diastereo- and enantioselectivity in the catalytic synthesis of beta-lactams. The Journal of Organic Chemistry. 69: 4531-3. PMID 15202914 DOI: 10.1021/Jo049804D |
0.802 |
|
| 2004 |
France S, Wack H, Taggi AE, Hafez AM, Wagerle TR, Shah MH, Dusich CL, Lectka T. Catalytic, asymmetric alpha-chlorination of acid halides. Journal of the American Chemical Society. 126: 4245-55. PMID 15053614 DOI: 10.1021/Ja039046T |
0.834 |
|
| 2004 |
France S, Weatherwax A, Taggi AE, Lectka T. Advances in the Catalytic, Asymmetric Synthesis of β-Lactams Cheminform. 35. DOI: 10.1002/chin.200444286 |
0.647 |
|
| 2004 |
France S, Wack H, Taggi AE, Hafez AM, Wagerle TR, Shah MH, Dusich CL, Lectka T. Catalytic, Asymmetric α-Chlorination of Acid Halides. Cheminform. 35. DOI: 10.1002/chin.200432037 |
0.751 |
|
| 2003 |
France S, Guerin DJ, Miller SJ, Lectka T. Nucleophilic chiral amines as catalysts in asymmetric synthesis. Chemical Reviews. 103: 2985-3012. PMID 12914489 DOI: 10.1021/Cr020061A |
0.767 |
|
| 2003 |
Hafez AM, Dudding T, Wagerle TR, Shah MH, Taggi AE, Lectka T. A multistage, one-pot procedure mediated by a single catalyst: a new approach to the catalytic asymmetric synthesis of beta-amino acids. The Journal of Organic Chemistry. 68: 5819-25. PMID 12868913 DOI: 10.1021/Jo034150E |
0.839 |
|
| 2003 |
Taggi AE, Hafez AM, Lectka T. Alpha-imino esters: versatile substrates for the catalytic, asymmetric synthesis of alpha- and beta-amino acids and beta-lactams. Accounts of Chemical Research. 36: 10-9. PMID 12534300 DOI: 10.1021/Ar020137P |
0.818 |
|
| 2003 |
Shah MH, France S, Lectka T. Bicarbonate Salts as Cost-Effective Bases for the Synthesis of Ketenes and Their Synthetic Equivalents Applied to the Asymmetric Synthesis of β-Lactams Synlett. 1937-1939. DOI: 10.1055/S-2003-41497 |
0.392 |
|
| 2003 |
Taggi AE, Hafez AM, Lectka T. α-Imino Esters: Versatile Substrates for the Catalytic, Asymmetric Synthesis of α- and β-Amino Acids and β-Lactams Cheminform. 34. DOI: 10.1002/chin.200316293 |
0.731 |
|
| 2002 |
Hafez AM, Taggi AE, Lectka T. Sequential column asymmetric catalysis. Chemistry (Weinheim An Der Bergstrasse, Germany). 8: 4114-9. PMID 12298001 DOI: 10.1002/1521-3765(20020916)8:18<4114::Aid-Chem4114>3.0.Co;2-Q |
0.804 |
|
| 2002 |
Taggi AE, Hafez AM, Wack H, Young B, Ferraris D, Lectka T. The development of the first catalyzed reaction of ketenes and imines: catalytic, asymmetric synthesis of beta-lactams. Journal of the American Chemical Society. 124: 6626-35. PMID 12047183 DOI: 10.1021/Ja0258226 |
0.824 |
|
| 2002 |
France S, Wack H, Hafez AM, Taggi AE, Witsil DR, Lectka T. Bifunctional asymmetric catalysis: a tandem nucleophile/Lewis acid promoted synthesis of beta-lactams. Organic Letters. 4: 1603-5. PMID 11975639 DOI: 10.1021/Ol025805L |
0.828 |
|
| 2002 |
Taggi AE, Wack H, Hafez AM, France S, Lectka T. Generation of ketenes from acid chlorides using NaH/crown ether shuttle-deprotonation for use in asymmetric catalysis. Organic Letters. 4: 627-9. PMID 11843608 DOI: 10.1021/Ol0172525 |
0.834 |
|
| 2002 |
Dudding T, Hafez AM, Taggi AE, Wagerle TR, Lectka T. A catalyst that plays multiple roles: asymmetric synthesis of beta-substituted aspartic acid derivatives through a four-stage, one-pot procedure. Organic Letters. 4: 387-90. PMID 11820886 DOI: 10.1021/Ol017087T |
0.834 |
|
| 2002 |
Ferraris D, Young B, Cox C, Dudding T, Drury WJ, Ryzhkov L, Taggi AE, Lectka T. Catalytic, enantioselective alkylation of alpha-imino esters: the synthesis of nonnatural alpha-amino acid derivatives. Journal of the American Chemical Society. 124: 67-77. PMID 11772063 DOI: 10.1021/Ja016838J |
0.841 |
|
| 2002 |
Taggi AE, Hafez AM, Dudding T, Lectka T. Molecular mechanics calculations as predictors of enantioselectivity for chiral nucleophile catalyzed reactions Tetrahedron. 58: 8351-8356. DOI: 10.1016/S0040-4020(02)00987-0 |
0.819 |
|
| 2002 |
Stone MB, Chen Y, Rittner J, Yardimci H, Reich DH, Broholm C, Ferraris DV, Lectka T. Frustrated three-dimensional quantum spin liquid in CuHpCl Physical Review B - Condensed Matter and Materials Physics. 65: 644231-6442312. |
0.492 |
|
| 2001 |
Hafez AM, Taggi AE, Dudding T, Lectka T. Asymmetric catalysis on sequentially-linked columns. Journal of the American Chemical Society. 123: 10853-9. PMID 11686686 DOI: 10.1021/Ja016556J |
0.834 |
|
| 2001 |
Wack H, Taggi AE, Hafez AM, Drury WJ, Lectka T. Catalytic, asymmetric alpha-halogenation. Journal of the American Chemical Society. 123: 1531-2. PMID 11456741 DOI: 10.1021/Ja005791J |
0.786 |
|
| 2001 |
Hafez AM, Taggi AE, Wack H, Esterbrook J, Lectka T. Reactive ketenes through a carbonate/amine shuttle deprotonation strategy: catalytic, enantioselective alpha-bromination of acid chlorides. Organic Letters. 3: 2049-51. PMID 11418046 DOI: 10.1021/Ol0160147 |
0.821 |
|
| 2000 |
Cox C, Lectka T. Synthetic catalysis of amide isomerization. Accounts of Chemical Research. 33: 849-58. PMID 11123884 DOI: 10.1021/Ar990165G |
0.397 |
|
| 2000 |
Hafez AM, Taggi AE, Wack H, Drury WJ, Lectka T. Column asymmetric catalysis for beta-lactam synthesis. Organic Letters. 2: 3963-5. PMID 11112618 DOI: 10.1021/Ol006659R |
0.819 |
|
| 2000 |
Taggi AE, Hafez AM, Wack H, Young B, Drury WJ, Lectka T. Catalytic, asymmetric synthesis of β-lactams [11] Journal of the American Chemical Society. 122: 7831-7832. DOI: 10.1021/Ja001754G |
0.795 |
|
| 2000 |
Taggi AE, Hafez AM, Wack H, Young B, Drury III WJ, Lectka T. ChemInform Abstract: Catalytic, Asymmetric Synthesis of β-Lactams. Cheminform. 31: no-no. DOI: 10.1002/chin.200047107 |
0.735 |
|
| 1999 |
Cox C, Wack H, Lectka T. Strong Hydrogen Bonding to the Amide Nitrogen Atom in an "Amide Proton Sponge": Consequences for Structure and Reactivity. Angewandte Chemie (International Ed. in English). 38: 798-800. PMID 29711794 DOI: 10.1002/(Sici)1521-3773(19990315)38:6<798::Aid-Anie798>3.0.Co;2-W |
0.801 |
|
| 1999 |
Wack H, Drury WJ, Taggi AE, Ferraris D, Lectka T. Nucleophilic metal complexes as acylation catalysts: solvent-dependent "switch" mechanisms leading to the first catalyzed Staudinger reaction. Organic Letters. 1: 1985-8. PMID 10836055 DOI: 10.1021/Ol9903234 |
0.817 |
|
| 1999 |
Cox C, Lectka T. Intramolecular acid-catalyzed amide isomerization in aqueous solution. Organic Letters. 1: 749-52. PMID 10823201 DOI: 10.1021/Ol9901265 |
0.417 |
|
| 1999 |
Ferraris D, Dudding T, Young B, Drury WJ, Lectka T. Catalytic, enantioselective alkylations of N,O-acetals Journal of Organic Chemistry. 64: 2168-2169. DOI: 10.1021/Jo982421T |
0.794 |
|
| 1999 |
Cox C, Wack H, Lectka T. Nucleophilic catalysis of amide isomerization [17] Journal of the American Chemical Society. 121: 7963-7964. DOI: 10.1021/Ja991487I |
0.546 |
|
| 1999 |
Evans DA, Barnes DM, Johnson JS, Lectka T, Von Matt P, Miller SJ, Murry JA, Norcross RD, Shaughnessy EA, Campos KR. Bis(oxazoline) and bis(oxazolinyl)pyridine copper complexes as enantioselective Diels-Alder catalysts: Reaction scope and synthetic applications Journal of the American Chemical Society. 121: 7582-7594. DOI: 10.1021/Ja991191C |
0.818 |
|
| 1999 |
Evans DA, Miller SJ, Lectka T, Von Matt P. Chiral bis(oxazoline)copper(II) complexes as lewis acid catalysts for the enantioselective Diels-Alder reaction Journal of the American Chemical Society. 121: 7559-7573. DOI: 10.1021/Ja991190K |
0.649 |
|
| 1999 |
Ferraris D, Young B, Dudding T, Drury WJ, Lectka T. Catalytic, enantioselective alkylations of N,O- and N,N-acetals and hemiacetals Tetrahedron. 55: 8869-8882. DOI: 10.1016/S0040-4020(99)00450-0 |
0.823 |
|
| 1999 |
Cox C, Wack H, Lectka T. Eine starke Wasserstoffbrücke zu einem Amid-Stickstoffatom in einem „Amid-Protonenschwamm”: Konsequenzen für Struktur und Reaktivität Angewandte Chemie. 111: 864-867. DOI: 10.1002/(Sici)1521-3757(19990315)111:6<864::Aid-Ange864>3.0.Co;2-S |
0.768 |
|
| 1998 |
Ferraris D, Young B, Cox C, Drury III WJ, Dudding T, Lectka T. Diastereo- and Enantioselective Alkylation of alpha-Imino Esters with Enol Silanes Catalyzed by (R)-Tol-BINAP-CuClO(4).(MeCN)(2). The Journal of Organic Chemistry. 63: 6090-6091. PMID 11672229 DOI: 10.1021/Jo981079H |
0.804 |
|
| 1998 |
Cox C, Lectka T. Solvent Effects on the Barrier to Rotation in Carbamates. The Journal of Organic Chemistry. 63: 2426-2427. PMID 11672097 DOI: 10.1021/Jo9800863 |
0.496 |
|
| 1998 |
Ferraris D, Drury WJ, Cox C, Lectka T. "Orthogonal" Lewis Acids: Catalyzed Ring Opening and Rearrangement of Acylaziridines Journal of Organic Chemistry. 63: 4568-4569. DOI: 10.1021/Jo980558D |
0.803 |
|
| 1998 |
Drury WJ, Ferraris D, Cox C, Young B, Lectka T. A novel synthesis of α-amino acid derivatives through catalytic, enantioselective ene reactions of α-imino esters [16] Journal of the American Chemical Society. 120: 11006-11007. DOI: 10.1021/Ja982257R |
0.832 |
|
| 1998 |
Cox C, Lectka T. Intramolecular catalysis of amide isomerization: Kinetic consequences of the 5-NH- -N(a) hydrogen bond in prolyl peptides Journal of the American Chemical Society. 120: 10660-10668. DOI: 10.1021/Ja9815071 |
0.517 |
|
| 1998 |
Ferraris D, Young B, Dudding T, Lectka T. Catalytic, enantioselective alkylation of α-imino esters using late transition metal phosphine complexes as catalysts Journal of the American Chemical Society. 120: 4548-4549. DOI: 10.1021/Ja9802450 |
0.835 |
|
| 1997 |
Cox C, Young, VG, Lectka T. Intramolecular Catalysis of Amide Isomerization Journal of the American Chemical Society. 119: 2307-2308. DOI: 10.1021/Ja964017M |
0.541 |
|
| 1997 |
Ferraris D, Cox C, Anand R, Lectka T. C-F bond activation by aryl carbocations: Conclusive intramolecular fluoride shifts between carbon atoms in solution and the first examples of intermolecular fluoride ion abstractions Journal of the American Chemical Society. 119: 4319-4320. DOI: 10.1021/Ja963090+ |
0.64 |
|
| 1996 |
Cox C, Ferraris D, Murthy NN, Lectka T. Copper(II)-catalyzed amide isomerization: Evidence for N-coordination Journal of the American Chemical Society. 118: 5332-5333. DOI: 10.1021/Ja960693C |
0.657 |
|
| 1993 |
McMurry JE, Lectka T. Carbocations with bent three-center, two-electron carbon-hydrogen-carbon bonds Journal of the American Chemical Society. 115: 10167-10173. DOI: 10.1021/Ja00075A036 |
0.615 |
|
| 1993 |
Evans DA, Miller SJ, Lectka T. Bis(oxazoline)copper(II) complexes as chiral catalysts for the enantioselective Diels-Alder reaction Journal of the American Chemical Society. 115: 6460-6461. DOI: 10.1021/Ja00067A091 |
0.633 |
|
| 1993 |
Evans DA, Lectka T, Miller SJ. Bis(imine)-copper(II) complexes as chiral lewis acid catalysts for the Diels-Alder reaction Tetrahedron Letters. 34: 7027-7030. DOI: 10.1016/S0040-4039(00)61588-5 |
0.606 |
|
| 1993 |
McMurry JE, Lectka T. Carbocations with bent three-center, two-electron C-H-C bonds Journal of the American Chemical Society. 115: 10167-10173. |
0.565 |
|
| 1992 |
Mcmurry JE, Lectka T. Three-center, two-electron C-H-C bonds in organic chemistry Accounts of Chemical Research. 25: 47-53. DOI: 10.1021/Ar00013A007 |
0.608 |
|
| 1990 |
McMurry JE, Lectka T. A remarkable alkane protonolysis reaction: Observation of stoichiometric hydrogen formation Journal of the American Chemical Society. 112: 869-870. DOI: 10.1021/Ja00158A058 |
0.626 |
|
| 1989 |
McMurry JE, Lectka T, Rico JG. An optimized procedure for titanium-induced carbonyl coupling Journal of Organic Chemistry. 54: 3748-3749. DOI: 10.1021/Jo00276A047 |
0.576 |
|
| 1989 |
McMurry JE, Lectka T, Hodge CN. The in-bicyclo[4.4.4]-1-tetradecyl cation: a stable substance with a three-center, two-electron carbon-hydrogen-carbon bond Journal of the American Chemical Society. 111: 8867-8872. DOI: 10.1021/Ja00206A015 |
0.594 |
|
| 1989 |
McMurry JE, Lectka T, Hodge CN. The in-bicyclo[4.4.4]-1-tetradecyl cation: A stable substance with a three-center, two-electron C-H-C bond Journal of the American Chemical Society. 111: 8867-8872. |
0.57 |
|
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