| Year |
Citation |
Score |
| 2024 |
Purohit V, Steussy CN, Rosales AR, Critchelow CJ, Schmidt T, Helquist P, Wiest O, Mesecar A, Cohen AE, Stauffacher CV. pH-dependent reaction triggering in PmHMGR crystals for time-resolved crystallography. Biophysical Journal. PMID 38327055 DOI: 10.1016/j.bpj.2024.02.003 |
0.652 |
|
| 2023 |
Patel HN, Haines BE, Stauffacher CV, Helquist P, Wiest O. Computational Study of Base-Catalyzed Thiohemiacetal Decomposition in HMG-CoA Reductase. The Journal of Physical Chemistry. B. PMID 37219997 DOI: 10.1021/acs.jpcb.2c08969 |
0.812 |
|
| 2023 |
Saebi M, Nan B, Herr JE, Wahlers J, Guo Z, Zurański AM, Kogej T, Norrby PO, Doyle AG, Chawla NV, Wiest O. On the use of real-world datasets for reaction yield prediction. Chemical Science. 14: 4997-5005. PMID 37206399 DOI: 10.1039/d2sc06041h |
0.641 |
|
| 2023 |
Maloney MP, Coley CW, Genheden S, Carson N, Helquist P, Norrby PO, Wiest O. Negative Data in Data Sets for Machine Learning Training. Organic Letters. 25: 2945-2947. PMID 37126483 DOI: 10.1021/acs.orglett.3c01282 |
0.748 |
|
| 2023 |
Maloney MP, Coley CW, Genheden S, Carson N, Helquist P, Norrby PO, Wiest O. Negative Data in Data Sets for Machine Learning Training. The Journal of Organic Chemistry. 88: 5239-5241. PMID 37126471 DOI: 10.1021/acs.joc.3c00844 |
0.748 |
|
| 2022 |
Wahlers J, Rosales AR, Berkel N, Forbes A, Helquist P, Norrby PO, Wiest O. A Quantum-Guided Molecular Mechanics Force Field for the Ferrocene Scaffold. The Journal of Organic Chemistry. 87: 12334-12341. PMID 36066498 DOI: 10.1021/acs.joc.2c01553 |
0.784 |
|
| 2022 |
Quinn TR, Patel HN, Koh KH, Haines BE, Norrby PO, Helquist P, Wiest O. Automated fitting of transition state force fields for biomolecular simulations. Plos One. 17: e0264960. PMID 35271647 DOI: 10.1371/journal.pone.0264960 |
0.802 |
|
| 2021 |
Wahlers J, Margalef J, Hansen E, Bayesteh A, Helquist P, Diéguez M, Pàmies O, Wiest O, Norrby PO. Proofreading experimentally assigned stereochemistry through Q2MM predictions in Pd-catalyzed allylic aminations. Nature Communications. 12: 6719. PMID 34795274 DOI: 10.1038/s41467-021-27065-2 |
0.814 |
|
| 2021 |
Pipalia NH, Saad SZ, Subramanian K, Cross A, Al-Motawa A, Garg K, Blagg BSJ, Neckers L, Helquist P, Wiest O, Ory DS, Maxfield FR. HSP90 inhibitors reduce cholesterol storage in Niemann-Pick type C1 mutant fibroblasts. Journal of Lipid Research. 100114. PMID 34481829 DOI: 10.1016/j.jlr.2021.100114 |
0.601 |
|
| 2021 |
Cruz DL, Pipalia N, Mao S, Gadi D, Liu G, Grigalunas M, O'Neill M, Quinn TR, Kipper A, Ekebergh A, Dimmling A, Gartner C, Melancon BJ, Wagner FF, Holson E, ... ... Wiest O, et al. Inhibition of Histone Deacetylases 1, 2, and 3 Enhances Clearance of Cholesterol Accumulation in Niemann-Pick C1 Fibroblasts. Acs Pharmacology & Translational Science. 4: 1136-1148. PMID 34151204 DOI: 10.1021/acsptsci.1c00033 |
0.602 |
|
| 2021 |
Quinn TR, Steussy CN, Haines BE, Lei J, Wang W, Sheong FK, Stauffacher CV, Huang X, Norrby PO, Helquist P, Wiest O. Microsecond timescale MD simulations at the transition state of HMGR predict remote allosteric residues. Chemical Science. 12: 6413-6418. PMID 34084441 DOI: 10.1039/d1sc00102g |
0.793 |
|
| 2021 |
Wahlers J, Maloney M, Salahi F, Rosales AR, Helquist P, Norrby PO, Wiest O. Stereoselectivity Predictions for the Pd-Catalyzed 1,4-Conjugate Addition Using Quantum-Guided Molecular Mechanics. The Journal of Organic Chemistry. PMID 33769065 DOI: 10.1021/acs.joc.1c00136 |
0.789 |
|
| 2021 |
Quinn TR, Steussy CN, Haines BE, Lei J, Wang W, Sheong FK, Stauffacher CV, Huang X, Norrby P, Helquist P, Wiest O. Microsecond timescale MD simulations at the transition state of PmHMGR predict remote allosteric residues Chemical Science. 12: 6413-6418. DOI: 10.1039/D1SC00102G |
0.62 |
|
| 2020 |
Work EM, Ferraudi G, Kiefer L, Liu G, Grigalunas M, Bhardwaj A, Kaur R, Dempsey JM, Wüstner D, Helquist P, Wiest O. Design, Synthesis, and Evaluation of a Luminescent Cholesterol Mimic. The Journal of Organic Chemistry. PMID 33369429 DOI: 10.1021/acs.joc.0c02460 |
0.627 |
|
| 2020 |
Salahi F, Wiest O. Regioselective Alkylation of Pyridinium Riboses. European Journal of Organic Chemistry. 2020: 446-449. PMID 32457563 DOI: 10.1002/Ejoc.201901603 |
0.788 |
|
| 2020 |
Rosales A, Ross SP, Helquist P, Norrby PO, Sigman MS, Wiest O. Transition State Force Field for the Asymmetric Redox Relay Heck Reaction. Journal of the American Chemical Society. PMID 32249569 DOI: 10.1021/Jacs.0C01979 |
0.806 |
|
| 2020 |
Purohit V, Rosales T, Critchelow C, Steussy C, Schmidt T, Wiest O, Helquist P, Stauffacher CV. Developing a pH-Jump Chemical Triggering Method for Time-Resolved Diffraction in Bacterial HMG-CoA Reductase Biophysical Journal. 118: 137a. DOI: 10.1016/J.Bpj.2019.11.875 |
0.628 |
|
| 2019 |
Davidson J, Molitor E, Moores S, Gale SE, Subramanian K, Jiang X, Sidhu R, Kell P, Zhang J, Fujiwara H, Davidson C, Helquist P, Melancon BJ, Grigalunas M, Liu G, ... ... Wiest O, et al. 2-Hydroxypropyl-β-cyclodextrin is the active component in a triple combination formulation for treatment of Niemann-Pick C1 disease. Biochimica Et Biophysica Acta. Molecular and Cell Biology of Lipids. PMID 31051283 DOI: 10.1016/J.Bbalip.2019.04.011 |
0.76 |
|
| 2018 |
Le DN, Hansen E, Khan HA, Kim B, Wiest O, Dong VM. Hydrogenation catalyst generates cyclic peptide stereocentres in sequence. Nature Chemistry. PMID 30061616 DOI: 10.1038/S41557-018-0089-5 |
0.643 |
|
| 2018 |
Rosales AR, Quinn TR, Wahlers J, Tomberg A, Zhang X, Helquist P, Wiest O, Norrby PO. Application of Q2MM to predictions in stereoselective synthesis. Chemical Communications (Cambridge, England). PMID 29971313 DOI: 10.1039/C8Cc03695K |
0.802 |
|
| 2018 |
Salahi F, Purohit V, Ferraudi G, Stauffacher C, Wiest O, Helquist P. pHP-Tethered N-Acyl Carbamate: A Photocage for Nicotinamide. Organic Letters. 20: 2547-2550. PMID 29652162 DOI: 10.1021/Acs.Orglett.8B00697 |
0.768 |
|
| 2018 |
Rosales AR, Wahlers J, Limé E, Meadows RE, Leslie KW, Savin R, Bell F, Hansen E, Helquist P, Munday RH, Wiest O, Norrby P. Rapid virtual screening of enantioselective catalysts using CatVS Nature Catalysis. 2: 41-45. DOI: 10.1038/s41929-018-0193-3 |
0.762 |
|
| 2018 |
Zhang X, Tutkowski B, Oliver A, Helquist P, Wiest O. Mechanistic Study of the Nickel-Catalyzed α,β-Coupling of Saturated Ketones Acs Catalysis. 8: 1740-1747. DOI: 10.1021/Acscatal.7B04105 |
0.677 |
|
| 2017 |
Ma J, Rosales AR, Huang X, Harms K, Riedel R, Wiest O, Meggers E. Visible-Light-Activated Asymmetric β-C-H Functionalization of Acceptor-Substituted Ketones with 1,2-Dicarbonyl Compounds. Journal of the American Chemical Society. PMID 29161036 DOI: 10.1021/Jacs.7B09152 |
0.792 |
|
| 2017 |
Zhang X, Chen K, Wu YD, Wiest O. Protein dynamics and structural waters in bromodomains. Plos One. 12: e0186570. PMID 29077715 DOI: 10.1371/Journal.Pone.0186570 |
0.459 |
|
| 2017 |
Huang X, Quinn TR, Harms K, Webster RD, Zhang L, Wiest O, Meggers E. Direct Visible-Light-Excited Asymmetric Lewis Acid Catalysis of Intermolecular [2+2] Photocycloadditions. Journal of the American Chemical Society. PMID 28644024 DOI: 10.1021/Jacs.7B04363 |
0.335 |
|
| 2017 |
Tutkowski B, Meggers E, Wiest O. Understanding Rate Acceleration and Stereoinduction of an Asymmetric Giese Reaction Mediated by a Chiral Rhodium Catalyst. Journal of the American Chemical Society. PMID 28558465 DOI: 10.1021/Jacs.7B01786 |
0.354 |
|
| 2017 |
Zhang C, Tutkowski B, DeLuca RJ, Joyce LA, Wiest O, Sigman MS. Palladium-Catalyzed Enantioselective Heck Alkenylation of Trisubstituted Allylic Alkenols: A Redox-Relay Strategy to Construct Vicinal Stereocenters. Chemical Science. 8: 2277-2282. PMID 28435657 DOI: 10.1039/C6Sc04585E |
0.384 |
|
| 2017 |
Tutkowski B, Kerdphon S, Limé E, Helquist P, Andersson PG, Wiest O, Norrby P. Revisiting the Stereodetermining Step in Enantioselective Iridium-Catalyzed Imine Hydrogenation Acs Catalysis. 8: 615-623. DOI: 10.1021/Acscatal.7B02386 |
0.794 |
|
| 2016 |
Grigalunas M, Wiest O, Helquist P. Single-Flask Multicomponent Synthesis of Highly Substituted α-Pyrones via a Sequential Enolate Arylation and Alkenylation Strategy. Organic Letters. 18: 5724-5727. PMID 27768319 DOI: 10.1021/Acs.Orglett.6B02969 |
0.666 |
|
| 2016 |
Xu L, Zhang X, McCammant MS, Sigman MS, Wu YD, Wiest O. Mechanism and Selectivity in the Pd-Catalyzed Difunctionalization of Isoprene. The Journal of Organic Chemistry. PMID 27486829 DOI: 10.1021/Acs.Joc.6B01317 |
0.56 |
|
| 2016 |
Xu W, Arieno M, Löw H, Huang K, Xie X, Cruchter T, Ma Q, Xi J, Huang B, Wiest O, Gong L, Meggers E. Metal-Templated Design: Enantioselective Hydrogen-Bond-Driven Catalysis Requiring Only Parts-per-Million Catalyst Loading. Journal of the American Chemical Society. PMID 27336458 DOI: 10.1021/Jacs.6B02769 |
0.786 |
|
| 2016 |
Lee JM, Zhang X, Norrby PO, Helquist P, Wiest O. Stereoselectivity in (Acyloxy)borane-Catalyzed Mukaiyama Aldol Reactions. The Journal of Organic Chemistry. PMID 27247023 DOI: 10.1021/Acs.Joc.6B00594 |
0.812 |
|
| 2016 |
Hansen E, Lime E, Norrby PO, Wiest O. Anomeric Effects in Sulfamides. The Journal of Physical Chemistry. A. PMID 27135551 DOI: 10.1021/Acs.Jpca.6B02757 |
0.771 |
|
| 2016 |
Hansen E, Rosales AR, Tutkowski B, Norrby PO, Wiest O. Prediction of Stereochemistry using Q2MM. Accounts of Chemical Research. PMID 27064579 DOI: 10.1021/Acs.Accounts.6B00037 |
0.813 |
|
| 2015 |
Hilton MJ, Cheng B, Buckley BR, Xu L, Wiest O, Sigman MS. Relative reactivity of alkenyl alcohols in the palladium-catalyzed redox-relay Heck reaction. Tetrahedron. 71: 6513-6518. PMID 26392640 DOI: 10.1016/J.Tet.2015.05.020 |
0.323 |
|
| 2015 |
Grigalunas M, Norrby PO, Wiest O, Helquist P. Single-Flask Multicomponent Palladium-Catalyzed α,γ-Coupling of Ketone Enolates: Facile Preparation of Complex Carbon Scaffolds. Angewandte Chemie (International Ed. in English). 54: 11822-5. PMID 26276904 DOI: 10.1002/Anie.201505895 |
0.784 |
|
| 2015 |
Clausen DJ, Smith WB, Haines BE, Wiest O, Bradner JE, Williams RM. Modular synthesis and biological activity of pyridyl-based analogs of the potent Class I Histone Deacetylase Inhibitor Largazole. Bioorganic & Medicinal Chemistry. 23: 5061-74. PMID 26054247 DOI: 10.1016/J.Bmc.2015.03.063 |
0.693 |
|
| 2015 |
Grigalunas M, Ankner T, Norrby PO, Wiest O, Helquist P. Ni-Catalyzed Alkenylation of Ketone Enolates under Mild Conditions: Catalyst Identification and Optimization. Journal of the American Chemical Society. 137: 7019-22. PMID 26024472 DOI: 10.1021/Jacs.5B02945 |
0.785 |
|
| 2015 |
Byrd KM, Arieno MD, Kennelly ME, Estiu G, Wiest O, Helquist P. Design and synthesis of a crosslinker for studying intracellular steroid trafficking pathways. Bioorganic & Medicinal Chemistry. 23: 3843-51. PMID 25890696 DOI: 10.1016/J.Bmc.2015.03.053 |
0.758 |
|
| 2015 |
Decroos C, Clausen DJ, Haines BE, Wiest O, Williams RM, Christianson DW. Variable active site loop conformations accommodate the binding of macrocyclic largazole analogues to HDAC8. Biochemistry. 54: 2126-35. PMID 25793284 DOI: 10.1021/Acs.Biochem.5B00010 |
0.697 |
|
| 2015 |
Tutkowski BM, Grigalunas M, Wiest O, Helquist P. A nickel-catalyzed α,β-coupling of saturated ketones Tetrahedron Letters. 56: 3468-3472. DOI: 10.1016/J.Tetlet.2015.02.061 |
0.681 |
|
| 2015 |
Tutkowski BM, Grigalunas M, Wiest O, Helquist P. ChemInform Abstract: A Nickel-Catalyzed α,β-Coupling of Saturated Ketones. Cheminform. 46: no-no. DOI: 10.1002/chin.201538102 |
0.608 |
|
| 2014 |
Limé E, Lundholm MD, Forbes A, Wiest O, Helquist P, Norrby PO. Stereoselectivity in Asymmetric Catalysis: The Case of Ruthenium-Catalyzed Ketone Hydrogenation. Journal of Chemical Theory and Computation. 10: 2427-35. PMID 26580763 DOI: 10.1021/Ct500178W |
0.807 |
|
| 2014 |
Hilton MJ, Xu LP, Norrby PO, Wu YD, Wiest O, Sigman MS. Investigating the nature of palladium chain-walking in the enantioselective redox-relay Heck reaction of alkenyl alcohols. The Journal of Organic Chemistry. 79: 11841-50. PMID 25186804 DOI: 10.1021/Jo501813D |
0.783 |
|
| 2014 |
Chen K, Zhang X, Wu YD, Wiest O. Inhibition and mechanism of HDAC8 revisited. Journal of the American Chemical Society. 136: 11636-43. PMID 25060069 DOI: 10.1021/Ja501548P |
0.431 |
|
| 2014 |
Grigalunas M, Ankner T, Norrby PO, Wiest O, Helquist P. Palladium-catalyzed alkenylation of ketone enolates under mild conditions. Organic Letters. 16: 3970-3. PMID 25032503 DOI: 10.1021/Ol5017965 |
0.775 |
|
| 2014 |
Haines BE, Wiest O. SET-induced biaryl cross-coupling: an S(RN)1 reaction. The Journal of Organic Chemistry. 79: 2771-4. PMID 24564385 DOI: 10.1021/Jo500222D |
0.734 |
|
| 2014 |
Collins CG, Lee JM, Oliver AG, Wiest O, Smith BD. Internal and external stereoisomers of squaraine rotaxane endoperoxide: synthesis, chemical differences, and structural revision. The Journal of Organic Chemistry. 79: 1120-30. PMID 24428682 DOI: 10.1021/Jo402564K |
0.343 |
|
| 2014 |
Xu L, Hilton MJ, Zhang X, Norrby PO, Wu YD, Sigman MS, Wiest O. Mechanism, reactivity, and selectivity in palladium-catalyzed redox-relay Heck arylations of alkenyl alcohols. Journal of the American Chemical Society. 136: 1960-7. PMID 24410393 DOI: 10.1021/Ja4109616 |
0.738 |
|
| 2014 |
Limé E, Lundholm MD, Forbes A, Wiest O, Helquist P, Norrby PO. Stereoselectivity in asymmetric catalysis: The case of ruthenium-catalyzed ketone hydrogenation Journal of Chemical Theory and Computation. 10: 2427-2435. DOI: 10.1021/ct500178w |
0.769 |
|
| 2014 |
Forbes A, Verdolino V, Helquist P, Wiest O. Transition metal-catalyzed hydrogenations Computational Organometallic Chemistry. 61-112. DOI: 10.1007/978-3-642-25258-7_4 |
0.623 |
|
| 2013 |
Cheng GJ, Song LJ, Yang YF, Zhang X, Wiest O, Wu YD. Computational Studies on the Mechanism of the Copper-Catalyzed sp -CH Cross-Dehydrogenative Coupling Reaction. Chempluschem. 78: 943-951. PMID 31986718 DOI: 10.1002/Cplu.201300117 |
0.519 |
|
| 2013 |
Bourbon P, Peng Q, Ferraudi G, Stauffacher C, Wiest O, Helquist P. Development of carbamate-tethered coumarins as phototriggers for caged nicotinamide. Bioorganic & Medicinal Chemistry Letters. 23: 6321-4. PMID 24125882 DOI: 10.1016/J.Bmcl.2013.09.067 |
0.689 |
|
| 2013 |
Helquist P, Maxfield FR, Wiech NL, Wiest O. Treatment of Niemann--pick type C disease by histone deacetylase inhibitors. Neurotherapeutics : the Journal of the American Society For Experimental Neurotherapeutics. 10: 688-97. PMID 24048860 DOI: 10.1007/S13311-013-0217-2 |
0.628 |
|
| 2013 |
Haines BE, Wiest O, Stauffacher CV. The increasingly complex mechanism of HMG-CoA reductase. Accounts of Chemical Research. 46: 2416-26. PMID 23898905 DOI: 10.1021/Ar3003267 |
0.721 |
|
| 2013 |
Bourbon P, Peng Q, Ferraudi G, Stauffacher C, Wiest O, Helquist P. Synthesis and photochemical behavior of coumarin-caged cholesterol. Bioorganic & Medicinal Chemistry Letters. 23: 2162-5. PMID 23434228 DOI: 10.1016/J.Bmcl.2013.01.095 |
0.647 |
|
| 2013 |
Cosner CC, Bhaskara Reddy Iska V, Chatterjee A, Markiewicz JT, Corden SJ, Löfstedt J, Ankner T, Richer J, Hulett T, Schauer DJ, Wiest O, Helquist P. Evolution of concise and flexible synthetic strategies for trichostatic acid and the potent histone deacetylase inhibitor trichostatin A European Journal of Organic Chemistry. 162-172. DOI: 10.1002/Ejoc.201201233 |
0.679 |
|
| 2012 |
Wehrmann ZT, Hulett TW, Huegel KL, Vaughan KT, Wiest O, Helquist P, Goodson H. Quantitative comparison of the efficacy of various compounds in lowering intracellular cholesterol levels in Niemann-Pick type C fibroblasts. Plos One. 7: e48561. PMID 23144769 DOI: 10.1371/Journal.Pone.0048561 |
0.637 |
|
| 2012 |
Haines BE, Steussy CN, Stauffacher CV, Wiest O. Molecular modeling of the reaction pathway and hydride transfer reactions of HMG-CoA reductase. Biochemistry. 51: 7983-95. PMID 22971202 DOI: 10.1021/Bi3008593 |
0.756 |
|
| 2012 |
Lee JM, Helquist P, Wiest O. Diastereoselectivity in Lewis-acid-catalyzed Mukaiyama aldol reactions: a DFT study. Journal of the American Chemical Society. 134: 14973-81. PMID 22891640 DOI: 10.1021/Ja3052975 |
0.705 |
|
| 2012 |
Bourbon P, Peng Q, Ferraudi G, Stauffacher C, Wiest O, Helquist P. Synthesis, photophysical, photochemical, and computational studies of coumarin-labeled nicotinamide derivatives. The Journal of Organic Chemistry. 77: 2756-62. PMID 22360284 DOI: 10.1021/Jo2025527 |
0.679 |
|
| 2011 |
Wiest O, Helquist P. Chemistry. Striking a balance to control stereochemistry. Science (New York, N.Y.). 333: 1831-2. PMID 21960616 DOI: 10.1126/science.1211195 |
0.592 |
|
| 2011 |
Pipalia NH, Cosner CC, Huang A, Chatterjee A, Bourbon P, Farley N, Helquist P, Wiest O, Maxfield FR. Histone deacetylase inhibitor treatment dramatically reduces cholesterol accumulation in Niemann-Pick type C1 mutant human fibroblasts. Proceedings of the National Academy of Sciences of the United States of America. 108: 5620-5. PMID 21436030 DOI: 10.1073/Pnas.1014890108 |
0.636 |
|
| 2011 |
Wiest O, Helquist P. Chemistry: Striking a balance to control stereochemistry Science. 333: 1831-1832. DOI: 10.1126/Science.1211195 |
0.703 |
|
| 2011 |
Zuo C, Wiest O, Wu Y. Structures and conformations of heteroatom-bridged calixarenes Journal of Physical Organic Chemistry. 24: 1157-1165. DOI: 10.1002/Poc.1840 |
0.493 |
|
| 2010 |
Filippakopoulos P, Qi J, Picaud S, Shen Y, Smith WB, Fedorov O, Morse EM, Keates T, Hickman TT, Felletar I, Philpott M, Munro S, McKeown MR, Wang Y, Christie AL, ... ... Wiest O, et al. Selective inhibition of BET bromodomains. Nature. 468: 1067-73. PMID 20871596 DOI: 10.1038/Nature09504 |
0.453 |
|
| 2010 |
Markiewicz JT, Wiest O, Helquist P. Synthesis of primary aryl amines through a copper-assisted aromatic substitution reaction with sodium azide. The Journal of Organic Chemistry. 75: 4887-90. PMID 20568788 DOI: 10.1021/Jo101002P |
0.687 |
|
| 2010 |
Rosenbaum AI, Cosner CC, Mariani CJ, Maxfield FR, Wiest O, Helquist P. Thiadiazole carbamates: potent inhibitors of lysosomal acid lipase and potential Niemann-Pick type C disease therapeutics. Journal of Medicinal Chemistry. 53: 5281-9. PMID 20557099 DOI: 10.1021/Jm100499S |
0.666 |
|
| 2010 |
Homan KT, Balasubramaniam D, Zabell APR, Wiest O, Helquist P, Stauffacher CV. Identification of novel inhibitors for a low molecular weight protein tyrosine phosphatase via virtual screening Bioorganic and Medicinal Chemistry. 18: 5449-5456. PMID 20538467 DOI: 10.1016/J.Bmc.2010.04.050 |
0.647 |
|
| 2010 |
Markiewicz JT, Schauer DJ, Löfstedt J, Corden SJ, Wiest O, Helquist P. Synthesis of 4-methyldienoates using a vinylogous Horner-Wadsworth-Emmons reagent. Application to the synthesis of trichostatic acid. The Journal of Organic Chemistry. 75: 2061-4. PMID 20158219 DOI: 10.1021/Jo902422Y |
0.675 |
|
| 2010 |
Chatterjee A, Richer J, Hulett T, Iska VBR, Wiest O, Helquist P. An efficient synthesis of (±)-trichostatic acid and analogues: A new route to (±)-trichostatin A Organic Letters. 12: 832-834. PMID 20104892 DOI: 10.1021/Ol9029116 |
0.655 |
|
| 2010 |
Iska VBR, Verdolino V, Wiest O, Helquist P. Mild and efficient desymmetrization of diynes via hydroamination: Application to the synthesis of (±)-monomorine I Journal of Organic Chemistry. 75: 1325-1328. PMID 20088529 DOI: 10.1021/Jo902674J |
0.672 |
|
| 2010 |
Lill SON, Forbes A, Donoghue P, Verdolino V, Wiest O, Rydberg P, Norrby P. Application of Q2MM to Stereoselective Reactions Current Organic Chemistry. 14: 1629-1645. DOI: 10.2174/138527210793563224 |
0.791 |
|
| 2010 |
Verdolino V, Forbes A, Helquist P, Norrby PO, Wiest O. On the mechanism of the rhodium catalyzed acrylamide hydrogenation Journal of Molecular Catalysis a: Chemical. 324: 9-14. DOI: 10.1016/J.Molcata.2010.02.026 |
0.804 |
|
| 2010 |
WIEST O, HOUK KN. ChemInform Abstract: Density Functional Theory Calculations of Pericyclic Reaction Transition Structures Cheminform. 28: no-no. DOI: 10.1002/chin.199714335 |
0.362 |
|
| 2010 |
WIEST O, STECKHAN E. ChemInform Abstract: Electron Transfer Catalyzed Diels-Alder Reactions with 2-Vinylindoles. Cheminform. 24: no-no. DOI: 10.1002/chin.199340094 |
0.579 |
|
| 2010 |
Nilsson Lill SO, Forbes A, Donoghue P, Verdolino V, Wiest O, Rydberg P, Norrby PO. Application of q2mm to stereoselective reactions Current Organic Chemistry. 14: 1629-1645. |
0.792 |
|
| 2009 |
Cosner CC, Markiewicz JT, Bourbon P, Mariani CJ, Wiest O, Rujoi M, Rosenbaum AI, Huang AY, Maxfield FR, Helquist P. Investigation of N-aryl-3-alkylidenepyrrolinones as potential Niemann-Pick type C disease therapeutics. Journal of Medicinal Chemistry. 52: 6494-8. PMID 19772346 DOI: 10.1021/Jm900707N |
0.649 |
|
| 2009 |
Zuo CS, Wiest O, Wu YD. Parameterization and validation of solvation corrected atomic radii. The Journal of Physical Chemistry. A. 113: 12028-34. PMID 19719098 DOI: 10.1021/Jp905865G |
0.478 |
|
| 2009 |
Lan Y, Deng L, Liu J, Wang C, Wiest O, Yang Z, Wu YD. On the mechanism of the palladium catalyzed intramolecular Pauson-Khand-type reaction. The Journal of Organic Chemistry. 74: 5049-58. PMID 19469502 DOI: 10.1021/Jo900919V |
0.563 |
|
| 2009 |
Wiech NL, Fisher JF, Helquist P, Wiest O. Inhibition of histone deacetylases: A pharmacological approach to the treatment of non-cancer disorders Current Topics in Medicinal Chemistry. 9: 257-271. PMID 19355990 DOI: 10.2174/156802609788085241 |
0.63 |
|
| 2009 |
Donoghue PJ, Helquist P, Norrby PO, Wiest O. Prediction of enantioselectivity in rhodium catalyzed hydrogenations. Journal of the American Chemical Society. 131: 410-1. PMID 19140780 DOI: 10.1021/Ja806246H |
0.791 |
|
| 2009 |
Helquist P, Wiest O. Current status of drug therapy development for Niemann-Pick type C disease Drugs of the Future. 34: 315-331. DOI: 10.1358/Dof.2009.034.04.1352412 |
0.617 |
|
| 2008 |
Donoghue PJ, Helquist P, Norrby PO, Wiest O. Development of a Q2MM Force Field for the Asymmetric Rhodium Catalyzed Hydrogenation of Enamides. Journal of Chemical Theory and Computation. 4: 1313-23. PMID 26631706 DOI: 10.1021/Ct800132A |
0.809 |
|
| 2008 |
O'Daniel PI, Jefferson M, Wiest O, Seley-Radtke KL. A computational study of expanded heterocyclic nucleosides in DNA. Journal of Biomolecular Structure & Dynamics. 26: 283-92. PMID 18808194 DOI: 10.1080/07391102.2008.10507243 |
0.329 |
|
| 2008 |
Sevov CS, Wiest O. Selectivity in the electron transfer catalyzed Diels-Alder reaction of (R)-alpha-phellandrene and 4-methoxystyrene. The Journal of Organic Chemistry. 73: 7909-15. PMID 18785777 DOI: 10.1021/Jo8002562 |
0.765 |
|
| 2008 |
Carney JM, Donoghue PJ, Wuest WM, Wiest O, Helquist P. Intramolecular hydroamination of aminoalkynes with silver-phenanthroline catalysts. Organic Letters. 10: 3903-6. PMID 18662005 DOI: 10.1021/Ol801458G |
0.788 |
|
| 2008 |
Estiu G, Greenberg E, Harrison CB, Kwiatkowski NP, Mazitschek R, Bradner JE, Wiest O. Structural origin of selectivity in class II-selective histone deacetylase inhibitors. Journal of Medicinal Chemistry. 51: 2898-906. PMID 18412327 DOI: 10.1021/Jm7015254 |
0.541 |
|
| 2008 |
Plummer JM, Weitgenant JA, Noll BC, Lauher JW, Wiest O, Helquist P. Synthesis, structure, and metal complexation behavior of a new type of functionalized chiral phenanthroline derivative. The Journal of Organic Chemistry. 73: 3911-4. PMID 18399656 DOI: 10.1021/Jo702566M |
0.66 |
|
| 2008 |
O'Neil LL, Wiest O. Structures and energetics of base flipping of the thymine dimer depend on DNA sequence. The Journal of Physical Chemistry. B. 112: 4113-22. PMID 18335922 DOI: 10.1021/Jp7102935 |
0.668 |
|
| 2008 |
Chung LW, Wiest O, Wu YD. A theoretical study on the trans-addition intramolecular hydroacylation of 4-alkynals catalyzed by cationic rhodium complexes. The Journal of Organic Chemistry. 73: 2649-55. PMID 18324834 DOI: 10.1021/Jo702582J |
0.556 |
|
| 2008 |
O'Neil LL, Wiest O. Sequence dependence in base flipping: experimental and computational studies. Organic & Biomolecular Chemistry. 6: 485-92. PMID 18219418 DOI: 10.1039/B713318A |
0.671 |
|
| 2008 |
Donoghue PJ, Helquist P, Norrby PO, Wiest O. Development of a Q2MM force field for the asymmetric rhodium catalyzed hydrogenation of enamides Journal of Chemical Theory and Computation. 4: 1313-1323. DOI: 10.1021/ct800132a |
0.782 |
|
| 2007 |
O'Neil LL, Grossfield A, Wiest O. Base flipping of the thymine dimer in duplex DNA. The Journal of Physical Chemistry. B. 111: 11843-9. PMID 17867670 DOI: 10.1021/Jp074043E |
0.673 |
|
| 2007 |
Wang D, Helquist P, Wiest O. Zinc binding in HDAC inhibitors: A DFT study Journal of Organic Chemistry. 72: 5446-5449. PMID 17579460 DOI: 10.1021/Jo070739S |
0.655 |
|
| 2007 |
Donoghue PJ, Helquist P, Wiest O. Ligand and substrate effects on the mechanism of rhodium-catalyzed hydrogenation of enamides. The Journal of Organic Chemistry. 72: 839-47. PMID 17253803 DOI: 10.1021/Jo0619276 |
0.794 |
|
| 2007 |
Fortner KC, Laitar DS, Muldoon J, Pu L, Braun-Sand SB, Wiest O, Brown SN. Ultrafast and ultraslow oxygen atom transfer reactions between late metal centers. Journal of the American Chemical Society. 129: 588-600. PMID 17227022 DOI: 10.1021/Ja065713H |
0.75 |
|
| 2007 |
Valley NA, Wiest O. Methyl substituent effects in radical cation Diels-Alder reactions. The Journal of Organic Chemistry. 72: 559-66. PMID 17221974 DOI: 10.1021/Jo0620361 |
0.362 |
|
| 2007 |
Donoghue PJ, Kieken E, Helquist P, Wiest O. Development of a Q2MM force field for the silver(I)-catalyzed hydroamination of alkynes Advanced Synthesis and Catalysis. 349: 2647-2654. DOI: 10.1002/Adsc.200700374 |
0.807 |
|
| 2006 |
O'Neil LL, Wiest O. Acyclic or long-bond intermediate in the electron-transfer-catalyzed dimerization of 4-methoxystyrene. The Journal of Organic Chemistry. 71: 8926-33. PMID 17081024 DOI: 10.1021/Jo061745B |
0.719 |
|
| 2006 |
Donoghue PJ, Wiest O. Structure and reactivity of radical ions: new twists on old concepts. Chemistry (Weinheim An Der Bergstrasse, Germany). 12: 7018-26. PMID 16874832 DOI: 10.1002/Chem.200600554 |
0.805 |
|
| 2006 |
Weitgenant JA, Katsuyama I, Bigi MA, Corden SJ, Markiewicz JT, Zabell APR, Homan KT, Wiest O, Stauffacher CV, Helquist P. Synthesis of a 5-azaindole phosphonic acid as a computationally designed inhibitor of the low molecular weight phosphatase HCPTP Heterocycles. 70: 599-607. DOI: 10.3987/Com-06-S(W)38 |
0.651 |
|
| 2006 |
Saettel NJ, Wiest O. Explicit and implicit solvation of radical ions: the cycloreversion of CPD dimers Tetrahedron. 62: 6490-6500. DOI: 10.1016/J.Tet.2006.03.059 |
0.742 |
|
| 2005 |
Harrison CB, O'Neil LL, Wiest O. Computational studies of DNA photolyase. The Journal of Physical Chemistry. A. 109: 7001-12. PMID 16834063 DOI: 10.1021/Jp051075Y |
0.747 |
|
| 2005 |
Nicolaescu AR, Wiest O, Kamat PV. Mechanistic pathways of the hydroxyl radical reactions of quinoline. 2. Computational analysis of hydroxyl radical attack at C atoms. The Journal of Physical Chemistry. A. 109: 2829-35. PMID 16833597 DOI: 10.1021/Jp045016G |
0.354 |
|
| 2005 |
Nicolaescu AR, Wiest O, Kamat PV. Mechanistic pathways of the hydroxyl radical reactions of quinoline. 1. Identification, distribution, and yields of hydroxylated products. The Journal of Physical Chemistry. A. 109: 2822-8. PMID 16833596 DOI: 10.1021/Jp0450179 |
0.331 |
|
| 2005 |
O'Neil LL, Wiest O. A selective, noncovalent assay for base flipping in DNA. Journal of the American Chemical Society. 127: 16800-1. PMID 16316222 DOI: 10.1021/Ja056274+ |
0.667 |
|
| 2005 |
Wang DF, Helquist P, Wiech NL, Wiest O. Toward selective histone deacetylase inhibitor design: homology modeling, docking studies, and molecular dynamics simulations of human class I histone deacetylases. Journal of Medicinal Chemistry. 48: 6936-47. PMID 16250652 DOI: 10.1021/Jm0505011 |
0.642 |
|
| 2005 |
Wright SK, DeClue MS, Mandal A, Lee L, Wiest O, Cleland WW, Hilvert D. Isotope effects on the enzymatic and nonenzymatic reactions of chorismate. Journal of the American Chemical Society. 127: 12957-64. PMID 16159290 DOI: 10.1021/Ja052929V |
0.315 |
|
| 2005 |
Kieken E, Wiest O, Helquist P, Cucciolito ME, Flores G, Vitagliano A, Norrby PO. Chiral diamine-silver (I)-alkene complexes: A quantum chemical and NMR study Organometallics. 24: 3737-3745. DOI: 10.1021/Om050275T |
0.785 |
|
| 2004 |
Wiest O, Harrison CB, Saettel NJ, Cibulka R, Sax M, König B. Design, synthesis, and evaluation of a biomimetic artificial photolyase model. The Journal of Organic Chemistry. 69: 8183-5. PMID 15549785 DOI: 10.1021/Jo0494329 |
0.782 |
|
| 2004 |
Wang DF, Wiest O, Helquist P, Lan-Hargest HY, Wiech NL. On the function of the 14 A long internal cavity of histone deacetylase-like protein: implications for the design of histone deacetylase inhibitors. Journal of Medicinal Chemistry. 47: 3409-17. PMID 15189037 DOI: 10.1021/Jm0498497 |
0.653 |
|
| 2004 |
Ding P, Miller MJ, Chen Y, Helquist P, Oliver AJ, Wiest O. Syntheses of conformationally constricted molecules as potential NAALADase/PSMA inhibitors. Organic Letters. 6: 1805-8. PMID 15151419 DOI: 10.1021/Ol049473R |
0.667 |
|
| 2004 |
Zabell APR, Corden S, Helquist P, Stauffacher CV, Wiest O. Inhibition studies with rationally designed inhibitors of the human low molecular weight protein tyrosine phosphatase Bioorganic and Medicinal Chemistry. 12: 1867-1880. PMID 15051056 DOI: 10.1016/J.Bmc.2004.01.042 |
0.66 |
|
| 2004 |
Wang DF, Wiest O, Helquist P, Lan-Hargest HY, Wiech NL. QSAR studies of PC-3 cell line inhibition activity of TSA and SAHA-like hydroxamic acids. Bioorganic & Medicinal Chemistry Letters. 14: 707-11. PMID 14741273 DOI: 10.1016/J.Bmcl.2003.11.062 |
0.648 |
|
| 2004 |
Pauvert M, Laine P, Jonas M, Wiest O. Toward an artificial oxidative DNA photolyase. The Journal of Organic Chemistry. 69: 543-8. PMID 14725471 DOI: 10.1021/Jo0354600 |
0.323 |
|
| 2004 |
Peller J, Wiest O, Kamat PV. Hydroxyl Radical's Role in the Remediation of a Common Herbicide, 2,4-Dichlorophenoxyacetic Acid (2,4-D) The Journal of Physical Chemistry A. 108: 10925-10933. DOI: 10.1021/Jp046450L |
0.696 |
|
| 2003 |
Peller J, Wiest O, Kamat PV. Mechanism of hydroxyl radical-induced breakdown of the herbicide 2,4-dichlorophenoxyacetic acid (2,4-d). Chemistry (Weinheim An Der Bergstrasse, Germany). 9: 5379-87. PMID 14613148 DOI: 10.1002/Chem.200204469 |
0.719 |
|
| 2003 |
Oliver AJ, Wiest O, Helquist P, Miller MJ, Tenniswood M. Conformational and SAR analysis of NAALADase and PSMA inhibitors. Bioorganic & Medicinal Chemistry. 11: 4455-61. PMID 13129582 DOI: 10.1016/S0968-0896(03)00427-9 |
0.658 |
|
| 2003 |
Peller J, Wiest O, Kamat PV. Synergy of combining sonolysis and photocatalysis in the degradation and mineralization of chlorinated aromatic compounds. Environmental Science & Technology. 37: 1926-32. PMID 12775067 DOI: 10.1021/Es0261630 |
0.706 |
|
| 2003 |
Saettel NJ, Wiest O. Sterically crowded bicyclo[1.1.0]butane radical cations. The Journal of Organic Chemistry. 68: 4549-52. PMID 12762768 DOI: 10.1021/Jo0267549 |
0.716 |
|
| 2003 |
Braun-Sand SB, Wiest O. Biasing Mixed-Valence Transition Metal Complexes in Search of Bistable Complexes for Molecular Computing Journal of Physical Chemistry B. 107: 9624-9628. DOI: 10.1021/Jp034208T |
0.752 |
|
| 2003 |
Braun-Sand SB, Wiest O. Theoretical studies of mixed-valence transition metal complexes for molecular computing Journal of Physical Chemistry A. 107: 285-291. DOI: 10.1021/Jp0265945 |
0.769 |
|
| 2003 |
Wiest O, Oxgaard J, Saettel NJ. Structure and reactivity of hydrocarbon radical cations Advances in Physical Organic Chemistry. 38: 87-109. DOI: 10.1016/S0065-3160(03)38002-5 |
0.801 |
|
| 2003 |
Oxgaard J, Wiest O. Substituent Effects in the Vinylcyclopropane Radical Cation Rearrangement: A Computational Road to a New Synthetic Tool European Journal of Organic Chemistry. 2003: 1454-1462. DOI: 10.1002/Ejoc.200390204 |
0.694 |
|
| 2002 |
Saettel NJ, Wiest O, Singleton DA, Meyer MP. Isotope effects and the mechanism of an electron-transfer-catalyzed Diels-Alder reaction. Journal of the American Chemical Society. 124: 11552-9. PMID 12236770 DOI: 10.1021/Ja026924Z |
0.745 |
|
| 2002 |
Wandel H, Wiest O. Enediynes in 11-membered rings. Synthesis, structure, and reactivity of highly strained but unusually stable macrocycles. Journal of Organic Chemistry. 67: 388-393. PMID 11798308 DOI: 10.1021/Jo0106041 |
0.306 |
|
| 2002 |
Stauffacher CV, Zabell APR, Katsuyama I, Helquist P, Wiest O. Computationally designed inhibitors of the low molecular weight phosphatase HCPTP Acta Crystallographica Section a Foundations of Crystallography. 58: c62-c62. DOI: 10.1107/S0108767302087561 |
0.594 |
|
| 2002 |
Oxgaard J, Wiest O. Rehybridized 1,3-butadiene radical cations: How far will a radical cation go to maintain conjugation? Journal of Physical Chemistry A. 106: 3967-3974. DOI: 10.1021/Jp020041C |
0.678 |
|
| 2001 |
Shireman BT, Miller MJ, Jonas M, Wiest O. Conformational study and enantioselective, regiospecific syntheses of novel aminoxy trans-proline analogues derived from an acylnitroso Diels-Alder cycloaddition. The Journal of Organic Chemistry. 66: 6046-56. PMID 11529730 DOI: 10.1021/Jo010284L |
0.352 |
|
| 2001 |
Radosevich AT, Wiest O. Quantum mechanical study of the ring-closing reaction of the hexatriene radical cation. The Journal of Organic Chemistry. 66: 5808-13. PMID 11511256 DOI: 10.1021/Jo0103524 |
0.701 |
|
| 2001 |
Saettel NJ, Wiest O. DFT study of the [2+2] cycloreversion of uracil dimer anion radical: waters matter. Journal of the American Chemical Society. 123: 2693-4. PMID 11456951 DOI: 10.1021/Ja005775M |
0.689 |
|
| 2001 |
El-Bahraoui J, Wiest O, Feichtinger D, Plattner DA. Rate Enhancement and Enantioselectivity of the Jacobsen–Katsuki Epoxidation: The Significance of the Sixth Coordination Site Angewandte Chemie. 40: 2073-2076. PMID 11433447 DOI: 10.1002/1521-3773(20010601)40:11<2073::Aid-Anie2073>3.0.Co;2-Y |
0.317 |
|
| 2001 |
Oxgaard J, Wiest O. Symmetry, radical ions, and butadienes: Exploring the limits of density functional theory Journal of Physical Chemistry A. 105: 8236-8240. DOI: 10.1021/Jp011336D |
0.674 |
|
| 2001 |
Hirt UH, Schuster MFH, French AN, Wiest OG, Wirth T. Chiral hypervalent organo-iodine(III) compounds European Journal of Organic Chemistry. 1569-1579. DOI: 10.1002/1099-0690(200104)2001:8<1569::Aid-Ejoc1569>3.0.Co;2-T |
0.392 |
|
| 2001 |
Saettel NJ, Oxgaard J, Wiest O. Pericyclic Reactions of Radical Cations European Journal of Organic Chemistry. 2001: 1429-1439. DOI: 10.1002/1099-0690(200104)2001:8<1429::Aid-Ejoc1429>3.0.Co;2-6 |
0.812 |
|
| 2001 |
Saettel NJ, Oxgaard J, Wiest O. Pericyclic reactions of radical cations European Journal of Organic Chemistry. 1429-1439. |
0.795 |
|
| 2000 |
Swinarski DJ, Wiest O. Substituent effects in pericyclic reactions of radical cations: the ring opening of 3-substituted cyclobutene radical cations Journal of Organic Chemistry. 65: 6708-6714. PMID 11052123 DOI: 10.1021/Jo0009494 |
0.373 |
|
| 2000 |
Nendel M, Sperling D, Wiest O, Houk KN. Computational explorations of vinylcyclopropane-cyclopentene rearrangements and competing diradical stereoisomerizations Journal of Organic Chemistry. 65: 3259-3268. PMID 10843604 DOI: 10.1021/Jo991026F |
0.452 |
|
| 2000 |
Amaudrut J, Wiest O. Epoxide formation by ring closure of the cinnamyloxy radical Organic Letters. 2: 1251-4. PMID 10810720 DOI: 10.1021/Ol005749T |
0.702 |
|
| 2000 |
Saettel NJ, Wiest O. Ab initio studies of The Journal of Organic Chemistry. 65: 2331-6. PMID 10789443 DOI: 10.1021/Jo991488T |
0.727 |
|
| 2000 |
Saettel NJ, Wiest O. Ab initio studies of [1,5]-H shifts: Pentadiene and beyond Journal of Organic Chemistry. 65: 2331-2336. DOI: 10.1021/jo991488t |
0.654 |
|
| 2000 |
Amaudrut J, Wiest O. The thermal sulfenate-sulfoxide rearrangement: A radical pair mechanism Journal of the American Chemical Society. 122: 3367-3374. DOI: 10.1021/Ja9940928 |
0.725 |
|
| 2000 |
Plattner DA, Feichtinger D, El-Bahraoui J, Wiest O. Coordination chemistry of manganese–salen complexes studied by electrospray tandem mass spectrometry: the significance of axial ligands International Journal of Mass Spectrometry. 195: 351-362. DOI: 10.1016/S1387-3806(99)00218-3 |
0.328 |
|
| 1999 |
Reddy GD, Wiest O, Hudlicky T, Schapiro V, Gonzalez D. Electron Transfer Catalyzed [2 + 2] Cycloreversion of Benzene Dimers. The Journal of Organic Chemistry. 64: 2860-2863. PMID 11674357 DOI: 10.1021/Jo982398B |
0.336 |
|
| 1999 |
Wiest O. Structure and [2+2] Cycloreversion of the Cyclobutane Radical Cation Journal of Physical Chemistry A. 103: 7907-7911. DOI: 10.1021/Jp991917R |
0.391 |
|
| 1999 |
Oxgaard J, Wiest O. The vinylcyclopropane radical cation rearrangement and related: Reactions on the C5H8·+ hypersurface Journal of the American Chemical Society. 121: 11531-11537. DOI: 10.1021/Ja9923639 |
0.694 |
|
| 1999 |
Haberl U, Wiest O, Steckhan E. Ab initio studies of the radical cation Diels-Alder reaction Journal of the American Chemical Society. 121: 6730-6736. DOI: 10.1021/Ja983993Y |
0.605 |
|
| 1999 |
Haberl U, Steckhan E, Blechert S, Wiest O. Electron-transfer-induced Diels - Alder reactions of indole and exocyclic dienes: Synthesis and quantum-chemical studies Chemistry - a European Journal. 5: 2859-2865. DOI: 10.1002/(Sici)1521-3765(19991001)5:10<2859::Aid-Chem2859>3.0.Co;2-R |
0.629 |
|
| 1998 |
Amaudrut J, Pasto DJ, Wiest O. Theoretical Studies of the Sulfenate-Sulfoxide Rearrangement. The Journal of Organic Chemistry. 63: 6061-6064. PMID 11672219 DOI: 10.1021/Jo980547K |
0.69 |
|
| 1997 |
Kast P, Tewari YB, Wiest O, Hilvert D, Houk KN, Goldberg RN. Thermodynamics of the Conversion of Chorismate to Prephenate: Experimental Results and Theoretical Predictions The Journal of Physical Chemistry B. 101: 10976-10982. DOI: 10.1021/Jp972501L |
0.437 |
|
| 1997 |
Wiest O, Montiel DC, Houk KN. Quantum Mechanical Methods and the Interpretation and Prediction of Pericyclic Reaction Mechanisms The Journal of Physical Chemistry A. 101: 8378-8388. DOI: 10.1021/Jp9717610 |
0.514 |
|
| 1997 |
Wiest O. Ab Initio Studies Of The Ring-Opening Reaction Of The Cyclobutene Radical Cation Journal of the American Chemical Society. 119: 5713-5719. DOI: 10.1021/Ja964334T |
0.341 |
|
| 1996 |
Wiest O. Density functional theory studies of the methanol radical cation hypersurface Journal of Molecular Structure-Theochem. 368: 39-48. DOI: 10.1016/S0166-1280(96)90533-3 |
0.324 |
|
| 1996 |
Wiest O, Houk KN. Density functional theory calculations of pericyclic reaction transition structures Topics in Current Chemistry. 183: 1-24. DOI: 10.1007/3-540-61131-2_1 |
0.445 |
|
| 1995 |
Wiest O, Houk KN. Stabilization of the Transition State of the Chorismate-Prephenate Rearrangement: An ab Initio Study of Enzyme and Antibody Catalysis Journal of the American Chemical Society. 117: 11628-11639. DOI: 10.1021/Ja00152A002 |
0.39 |
|
| 1995 |
Wiest O, Houk KN, Black KA, Thomas B. Secondary Kinetic Isotope Effects of Diastereotopic Protons in Pericyclic Reactions: A New Mechanistic Probe Journal of the American Chemical Society. 117: 8594-8599. DOI: 10.1021/Ja00138A015 |
0.34 |
|
| 1994 |
Wiest O, Houk KN. On the Transition State of the Chorismate-Prephenate Rearrangement The Journal of Organic Chemistry. 59: 7582-7584. DOI: 10.1021/Jo00104A008 |
0.379 |
|
| 1994 |
Wiest O, Black KA, Houk KN. Density Functional Theory Isotope Effects and Activation Energies for the Cope and Claisen Rearrangements Journal of the American Chemical Society. 116: 10336-10337. DOI: 10.1021/Ja00101A078 |
0.374 |
|
| 1993 |
Wiest O, Steckhan E. Radical cation Diels-Alder reaction of indoles and exocyclic dienes Tetrahedron Letters. 34: 6391-6394. DOI: 10.1016/0040-4039(93)85053-Y |
0.636 |
|
| 1993 |
Wiest O, Steckhan E. Electron Transfer‐Catalyzed Diels–Alder Reactions with 2‐Vinylindoles Angewandte Chemie. 32: 901-903. DOI: 10.1002/Anie.199309011 |
0.601 |
|
| 1993 |
Wiest O, Steckhan E. Electron transfer-catalyzed Diels-Alder reactions with 2-vinylindoles Angewandte Chemie (International Edition in English). 32: 901-903. |
0.575 |
|
| 1992 |
Wiest O, Steckhan E, Grein F. Selectivity in radical-cation Diels-Alder reactions of indole and electron-rich dienes: A semiempirical approach Journal of Organic Chemistry. 57: 4034-4037. DOI: 10.1021/Jo00040A060 |
0.615 |
|
| 1991 |
Gieseler A, Steckhan E, Wiest O, Knoch F. Photochemically induced radical cation Diels-Alder reaction of indole and electron-rich dienes Journal of Organic Chemistry. 56: 1405-1411. DOI: 10.1021/Jo00004A013 |
0.619 |
|
| 1990 |
Gieseler A, Steckhan E, Wiest O. Photoinduced, Electron-Transfer-Catalyzed Diels-Alder Reaction Between Indole and 1,3-Cyclohexadienes1 Synlett. 1990: 275-277. DOI: 10.1055/S-1990-21063 |
0.618 |
|
| 1990 |
GIESELER A, STECKHAN E, WIEST O. ChemInform Abstract: Photoinduced, Electron-Transfer-Catalyzed Diels-Alder Reaction Between Indole and 1,3-Cyclohexadienes. Cheminform. 21. DOI: 10.1002/chin.199039168 |
0.581 |
|
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