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Karl A. Scheidt, Ph.D. - Publications

Affiliations: 
2002- Chemistry Northwestern University, Evanston, IL 
Area:
Organic, Synthetic, Bio-Organic, Medicinal Chemistry, Chemical Biology, Catalysis, Materials
Website:
https://chemistry.northwestern.edu/people/core-faculty/profiles/karl-scheidt.html
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224 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2025 Scheidt K, Cao J, Schull C. Deconstructive Radical-Radical Coupling for Programmable Remote Acylation. Angewandte Chemie (International Ed. in English). e202507542. PMID 40425491 DOI: 10.1002/anie.202507542  0.417
2023 Rourke MJ, McGill MJ, Yang D, Farnam EJ, Zhu JL, Scheidt KA. Photoredox-Catalyzed Radical-Radical Coupling of Potassium Trifluoroborates with Acyl Azoliums. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 34: 2175-2180. PMID 38948905 DOI: 10.1055/s-0041-1738448  0.808
2023 Nam Y, Tam AT, Miller ER, Scheidt KA. A Platform for the Synthesis of Corynantheine-Type Corynanthe Alkaloids. Journal of the American Chemical Society. PMID 38153983 DOI: 10.1021/jacs.3c12556  0.628
2023 Cao J, Zhu JL, Scheidt KA. Photoinduced cerium-catalyzed C-H acylation of unactivated alkanes. Chemical Science. 15: 154-159. PMID 38131082 DOI: 10.1039/d3sc05162e  0.371
2023 Rourke MJ, Wang CT, Schull CR, Scheidt KA. Acyl Azolium-Photoredox-Enabled Synthesis of -Keto Sulfides. Acs Catalysis. 13: 7987-7994. PMID 37969469 DOI: 10.1021/acscatal.3c01558  0.802
2023 Tanaka N, Zhu JL, Valencia OL, Schull CR, Scheidt KA. Cooperative Carbene Photocatalysis for β-Amino Ester Synthesis. Journal of the American Chemical Society. PMID 37906227 DOI: 10.1021/jacs.3c09875  0.821
2023 Byun S, Hwang MU, Wise HR, Bay AV, Cheong PH, Scheidt KA. Light-Driven Enantioselective Carbene-Catalyzed Radical-Radical Coupling. Angewandte Chemie (International Ed. in English). 62: e202312829. PMID 37845183 DOI: 10.1002/anie.202312829  0.639
2023 Kim DR, Orr MJ, Kwong AJ, Deibler KK, Munshi HH, Bridges CS, Chen TJ, Zhang X, Lacorazza HD, Scheidt KA. Rational Design of Highly Potent and Selective Covalent MAP2K7 Inhibitors. Acs Medicinal Chemistry Letters. 14: 606-613. PMID 37197477 DOI: 10.1021/acsmedchemlett.3c00029  0.78
2023 Zhu JL, Schull CR, Tam AT, Rentería-Gómez Á, Gogoi AR, Gutierrez O, Scheidt KA. Photoinduced Acylations Via Azolium-Promoted Intermolecular Hydrogen Atom Transfer. Journal of the American Chemical Society. 145: 1535-1541. PMID 36625715 DOI: 10.1021/jacs.2c12845  0.8
2022 Byun S, Farah AO, Wise HR, Katchmar A, Cheong PH, Scheidt KA. Enantioselective Copper-Catalyzed Borylative Amidation of Allenes. Journal of the American Chemical Society. PMID 36473196 DOI: 10.1021/jacs.2c10507  0.652
2022 Liu Y, Betori RC, Pagacz J, Frost GB, Efimova EV, Wu D, Wolfgeher DJ, Bryan TM, Cohen SB, Scheidt KA, Kron SJ. Targeting telomerase reverse transcriptase with the covalent inhibitor NU-1 confers immunogenic radiation sensitization. Cell Chemical Biology. PMID 36206753 DOI: 10.1016/j.chembiol.2022.09.002  0.765
2022 McCollum MM, Larmore M, Ishihara S, Ng LCT, Kimura LF, Guadarrama E, Ta MC, Vien TN, Frost GB, Scheidt KA, Miller RE, DeCaen PG. Targeting the tamoxifen receptor within sodium channels to block osteoarthritic pain. Cell Reports. 40: 111248. PMID 36001977 DOI: 10.1016/j.celrep.2022.111248  0.752
2022 Bay AV, Farnam EJ, Scheidt KA. Synthesis of Cyclohexanones by a Tandem Photocatalyzed Annulation. Journal of the American Chemical Society. 144: 7030-7037. PMID 35316053 DOI: 10.1021/jacs.1c13105  0.414
2021 Miller ER, Scheidt KA. Enantioselective Syntheses of Yohimbine Alkaloids: Proving Grounds for New Catalytic Transformations. Synthesis. 54: 1217-1230. PMID 36187077 DOI: 10.1055/a-1684-2942  0.609
2021 Wang P, Fitzpatrick KP, Scheidt KA. Combined Photoredox and Carbene Catalysis for the Synthesis of γ-Aryloxy Ketones. Advanced Synthesis & Catalysis. 364: 518-524. PMID 35431717 DOI: 10.1002/adsc.202101354  0.642
2021 Betori RC, McDonald BR, Scheidt KA. Correction: Reductive annulations of arylidene malonates with unsaturated electrophiles using photoredox/Lewis acid cooperative catalysis. Chemical Science. 12: 5688. PMID 35340933 DOI: 10.1039/d1sc90070f  0.757
2021 Scheidt K, Bay AV, Kitzpatrick KP, González-Montiel GA, Farah AO, Cheong PH. Light-Driven Carbene Catalysis for the Synthesis of Aliphatic and α-Amino Ketones. Angewandte Chemie (International Ed. in English). PMID 34097802 DOI: 10.1002/anie.202105354  0.626
2020 Zhu JL, Laws SW, Rourke MJ, Scheidt KA. Radical coupling of -ketoesters and amides promoted by Brønsted/Lewis acids. Green Synthesis and Catalysis. 1: 70-74. PMID 34485961 DOI: 10.1016/j.gresc.2020.06.003  0.815
2020 Maskeri MA, Brueckner AC, Feoktistova T, O'Connor MJ, Walden DM, Cheong PH, Scheidt KA. Mechanism and origins of selectivity in the enantioselective oxa-Pictet-Spengler reaction: a cooperative catalytic complex from a hydrogen bond donor and chiral phosphoric acid. Chemical Science. 11: 8736-8743. PMID 34123127 DOI: 10.1039/d0sc03250f  0.816
2020 Bayly AA, McDonald BR, Mrksich M, Scheidt KA. High-throughput photocapture approach for reaction discovery. Proceedings of the National Academy of Sciences of the United States of America. PMID 32482866 DOI: 10.1073/Pnas.2003347117  0.783
2020 Scheidt K, Davies A, Fitzpatrick K, Betori R. Combined Photoredox and Carbene Catalysis for the Synthesis of Ketones from Carboxylic Acids. Angewandte Chemie (International Ed. in English). PMID 32119162 DOI: 10.1002/Anie.202001824  0.658
2020 Maskeri MA, Schrader ML, Scheidt KA. A Sequential Umpolung/Enzymatic Dynamic Kinetic Resolution Strategy for the Synthesis of γ-Lactones. Chemistry (Weinheim An Der Bergstrasse, Germany). 26: 5794-5798. PMID 32084294 DOI: 10.1002/Chem.202000747  0.823
2020 Miller ER, Hovey MT, Scheidt KA. A Concise, Enantioselective Approach for the Synthesis of Yohimbine Alkaloids. Journal of the American Chemical Society. PMID 31951394 DOI: 10.1021/Jacs.9B12319  0.687
2020 Maskeri MA, Brueckner AC, Feoktistova T, O'Connor MJ, Walden DM, Cheong PH, Scheidt KA. Mechanism and origins of selectivity in the enantioselective oxa-Pictet–Spengler reaction: a cooperative catalytic complex from a hydrogen bond donor and chiral phosphoric acid Chemical Science. 11: 8736-8743. DOI: 10.1039/D0Sc03250F  0.816
2020 Fitzpatrick KP, Schwamb CB, Check CT, Jang KP, Barsoum DN, Scheidt KA. Development of Ferrocene-Based Planar Chiral Imidazopyridinium Salts for Catalysis Organometallics. 39: 2705-2712. DOI: 10.1021/Acs.Organomet.0C00312  0.364
2019 Mishra RK, Deibler KK, Clutter MR, Vagadia PP, O'Connor M, Schiltz GE, Bergan R, Scheidt KA. Modeling MEK4 Kinase Inhibitors Through Perturbed Electrostatic Potential (ESP) Charges. Journal of Chemical Information and Modeling. PMID 31566378 DOI: 10.1021/Acs.Jcim.9B00490  0.774
2019 Scheidt K, Betori R, May C. Combined Photoredox/Enzymatic C-H Benzylic Hydroxylations Rick C. Betoria, Catherine M. Maya, Karl A. Scheidt*a. Angewandte Chemie (International Ed. in English). PMID 31465617 DOI: 10.1002/Ange.201909426  0.305
2019 Scheidt K, Squitieri R, Fitzpatrick K, Jaworski A. Synthesis and Evaluation of Azolium-Based Halogen Bond Donors. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31112630 DOI: 10.1002/Chem.201902298  0.654
2019 Betori RC, McDonald BR, Scheidt KA. Reductive annulations of arylidene malonates with unsaturated electrophiles using photoredox/Lewis acid cooperative catalysis. Chemical Science. 10: 3353-3359. PMID 30996923 DOI: 10.1039/C9Sc00302A  0.798
2019 Scheidt K, Lee A, Zhu J, Feoktistova T, Brueckner A, Cheong P. Carbene-Catalyzed Enantioselective Decarboxylative Annulations to Access Dihydrobenzoxazinones and Quinolones. Angewandte Chemie (International Ed. in English). PMID 30843323 DOI: 10.1002/Anie.201900600  0.646
2019 Scheidt K, Deibler KK, Schiltz GE, Clutter MR, Mishra RK, Vagadia PP, O'Connor M, George MD, Gordon R, Fowler G, Bergan R. Synthesis and Biological Evaluation of 3-Arylindazoles as Selective MEK4 Inhibitors. Chemmedchem. PMID 30707493 DOI: 10.1002/Cmdc.201900019  0.78
2019 Betori RC, Scheidt KA. Reductive Arylation of Arylidene Malonates Using Photoredox Catalysis Acs Catalysis. 9: 10350-10357. DOI: 10.1021/Acscatal.9B03608  0.391
2018 Lopez SS, Jaworski AA, Scheidt KA. NHC-Catalyzed Formal [2+2] Annulations of Allenoates for the Synthesis of Substituted Oxetanes. The Journal of Organic Chemistry. PMID 30427675 DOI: 10.1021/Acs.Joc.8B02464  0.517
2018 Scheidt K, Maskeri M, O'Connor M, Jaworski AA, Davies A. A Cooperative Hydrogen Bond Donor/Brønsted Acid System for the Enantioselective Synthesis of Tetrahydropyrans. Angewandte Chemie (International Ed. in English). PMID 30380196 DOI: 10.1002/Anie.201811383  0.817
2018 McDonald BR, Scheidt KA. Intermolecular Reductive Couplings of Arylidene Malonates via Lewis Acid/Photoredox Cooperative Catalysis. Organic Letters. PMID 30346177 DOI: 10.1021/Acs.Orglett.8B02893  0.796
2018 Schwamb CB, Fitzpatrick KP, Brueckner AC, Richardson HC, Cheong PH, Scheidt KA. Correction to "Enantioselective Synthesis of α-Amidoboronates Catalyzed by Planar-Chiral NHC-Cu(I) Complexes". Journal of the American Chemical Society. PMID 30299942 DOI: 10.1021/Jacs.8B10073  0.728
2018 Schwamb CB, Fitzpatrick KP, Brueckner AC, Richardson HC, Cheong PH, Scheidt KA. Enantioselective Synthesis of α-Amidoboronates Catalyzed by Planar-Chiral NHC-Cu(I) Complexes. Journal of the American Chemical Society. PMID 30102526 DOI: 10.1021/Jacs.8B05045  0.749
2018 Xu L, Gordon R, Farmer R, Pattanayak A, Binkowski A, Huang X, Avram M, Krishna S, Voll E, Pavese J, Chavez J, Bruce J, Mazar A, Nibbs A, Anderson W, ... ... Scheidt K, et al. Precision therapeutic targeting of human cancer cell motility. Nature Communications. 9: 2454. PMID 29934502 DOI: 10.1038/S41467-018-04465-5  0.777
2018 Lee A, Betori R, Crane E, Scheidt KA. An Enantioselective Cross Dehydrogenative Coupling Catalysis Approach to Substituted Tetrahydropyrans. Journal of the American Chemical Society. PMID 29714480 DOI: 10.1021/Jacs.8B03063  0.795
2018 Uno BE, Dicken RD, Redfern LR, Stern CM, Krzywicki GG, Scheidt KA. Calcium(ii)-catalyzed enantioselective conjugate additions of amines. Chemical Science. 9: 1634-1639. PMID 29675209 DOI: 10.1039/C7Sc05205G  0.712
2018 Malik N, Iyamu ID, Scheidt KA, Schiltz GE. Synthesis of a novel fused pyrrolodiazepine-based library with anti-cancer activity. Tetrahedron Letters. 59: 1513-1516. PMID 29610541 DOI: 10.1016/J.Tetlet.2018.03.021  0.386
2018 Murauski KJR, Jaworski AA, Scheidt KA. A continuing challenge: N-heterocyclic carbene-catalyzed syntheses of γ-butyrolactones. Chemical Society Reviews. PMID 29372207 DOI: 10.1039/C7Cs00386B  0.5
2018 Uno BE, Deibler KK, Villa C, Raghuraman A, Scheidt KA. Conjugate Additions of Amines to Maleimides via Cooperative Catalysis Advanced Synthesis & Catalysis. 360: 1719-1725. DOI: 10.1002/Adsc.201800160  0.43
2017 Murauski KJR, Walden DM, Cheong PH, Scheidt KA. A Cooperative Ternary Catalysis System for Asymmetric Lactonizations of α-Ketoesters. Advanced Synthesis & Catalysis. 359: 3713-3719. PMID 30473657 DOI: 10.1002/Adsc.201701015  0.655
2017 Betori RC, Miller ER, Scheidt KA. A Biocatalytic Route to Highly Enantioenriched β-Hydroxydioxinones. Advanced Synthesis & Catalysis. 359: 1131-1137. PMID 29104524 DOI: 10.1002/Adsc.201700095  0.582
2017 Walden DM, Jaworski AA, Johnston RC, Hovey MT, Baker HV, Meyer MP, Scheidt KA, Cheong PH. On the Formation of Aza-ortho-quinone Methides Under Room Temperature Conditions: Cs2CO3 Effect. The Journal of Organic Chemistry. PMID 28649838 DOI: 10.1021/Acs.Joc.7B00697  0.741
2017 Scheidt K, Hovey T, Cohen D, Walden D, Cheong P. A Carbene Catalysis Strategy for the Synthesis of Protoilludane Natural Products. Angewandte Chemie (International Ed. in English). PMID 28632913 DOI: 10.1002/Anie.201705308  0.745
2017 Wang MH, Barsoum D, Schwamb CB, Cohen DT, Goess BC, Riedrich M, Chan A, Maki BE, Mishra RK, Scheidt KA. Catalytic, Enantioselective β-Protonation through a Cooperative Activation Strategy. The Journal of Organic Chemistry. PMID 28441019 DOI: 10.1021/Acs.Joc.7B00334  0.821
2017 Deibler KK, Mishra RK, Clutter MR, Antanasijevic A, Bergan R, Caffrey M, Scheidt KA. A Chemical Probe Strategy for Interrogating Inhibitor Selectivity Across the MEK kinase Family. Acs Chemical Biology. PMID 28263556 DOI: 10.1021/Acschembio.6B01060  0.777
2017 List B, Shevchenko GA, Betori RC, Miller ER, Scheidt KA. Biocatalytic Synthesis of β-Hydroxydioxinones Synfacts. 13: 539-1137. DOI: 10.1055/S-0036-1590378  0.328
2017 Beniah G, Chen X, Uno BE, Liu K, Leitsch EK, Jeon J, Heath WH, Scheidt KA, Torkelson JM. Combined Effects of Carbonate and Soft-Segment Molecular Structures on the Nanophase Separation and Properties of Segmented Polyhydroxyurethane Macromolecules. 50: 3193-3203. DOI: 10.1021/Acs.Macromol.6B02513  0.62
2017 Beniah G, Uno BE, Lan T, Jeon J, Heath WH, Scheidt KA, Torkelson JM. Tuning nanophase separation behavior in segmented polyhydroxyurethane via judicious choice of soft segment Polymer. 110: 218-227. DOI: 10.1016/J.Polymer.2017.01.017  0.59
2017 Betori RC, Miller ER, Scheidt KA. Front Cover Picture: A Biocatalytic Route to Highly Enantioenriched β‐Hydroxydioxinones (Adv. Synth. Catal. 7/2017) Advanced Synthesis & Catalysis. 359: 1065-1065. DOI: 10.1002/Adsc.201700229  0.309
2016 Wang MH, Scheidt KA. Cooperative Catalysis and Activation with N-Heterocyclic Carbenes. Angewandte Chemie (International Ed. in English). PMID 27763702 DOI: 10.1002/Anie.201605319  0.432
2016 Jaworski AA, Scheidt KA. Emerging Roles of in Situ Generated Quinone Methides in Metal-Free Catalysis. The Journal of Organic Chemistry. PMID 27513764 DOI: 10.1021/Acs.Joc.6B01367  0.341
2016 Sharma HA, Todd Hovey M, Scheidt KA. Azaindole synthesis through dual activation catalysis with N-heterocyclic carbenes. Chemical Communications (Cambridge, England). PMID 27363788 DOI: 10.1039/C6Cc04735A  0.713
2016 Leitsch EK, Beniah G, Liu K, Lan T, Heath WH, Scheidt KA, Torkelson JM. Nonisocyanate Thermoplastic Polyhydroxyurethane Elastomers via Cyclic Carbonate Aminolysis: Critical Role of Hydroxyl Groups in Controlling Nanophase Separation Acs Macro Letters. 5: 424-429. DOI: 10.1021/Acsmacrolett.6B00102  0.368
2016 Hall EA, Redfern LR, Wang MH, Scheidt KA. Lewis Acid Activation of a Hydrogen Bond Donor Metal-Organic Framework for Catalysis Acs Catalysis. 6: 3248-3252. DOI: 10.1021/Acscatal.6B00424  0.317
2016 Beniah G, Liu K, Heath WH, Miller MD, Scheidt KA, Torkelson JM. Novel thermoplastic polyhydroxyurethane elastomers as effective damping materials over broad temperature ranges European Polymer Journal. 84: 770-783. DOI: 10.1016/J.Eurpolymj.2016.05.031  0.35
2015 Wang MH, Cohen DT, Schwamb CB, Mishra RK, Scheidt KA. Enantioselective β-Protonation by a Cooperative Catalysis Strategy. Journal of the American Chemical Society. 137: 5891-4. PMID 25929160 DOI: 10.1055/S-0034-1381154  0.626
2015 Younai A, Zeng BS, Meltzer HY, Scheidt KA. Enantioselective Syntheses of Heteroyohimbine Natural Products: A Unified Approach through Cooperative Catalysis. Angewandte Chemie (International Ed. in English). 54: 6900-4. PMID 25914164 DOI: 10.1002/Anie.201502011  0.403
2015 McDonald BR, Scheidt KA. Pyranone natural products as inspirations for catalytic reaction discovery and development. Accounts of Chemical Research. 48: 1172-83. PMID 25742935 DOI: 10.1021/Ar5004576  0.835
2015 Lee A, Scheidt KA. N-Heterocyclic carbene-catalyzed enantioselective annulations: a dual activation strategy for a formal [4+2] addition for dihydrocoumarins. Chemical Communications (Cambridge, England). 51: 3407-10. PMID 25623173 DOI: 10.1039/C4Cc09590A  0.6
2015 Check CT, Jang KP, Schwamb CB, Wong AS, Wang MH, Scheidt KA. Ferrocene-based planar chiral imidazopyridinium salts for catalysis. Angewandte Chemie (International Ed. in English). 54: 4264-8. PMID 25619772 DOI: 10.1002/Anie.201410118  0.589
2015 Cohen DT, Johnston RC, Rosson NT, Cheong PH, Scheidt KA. Functionalized cyclopentenes through a tandem NHC-catalyzed dynamic kinetic resolution and ambient temperature decarboxylation: mechanistic insight and synthetic application. Chemical Communications (Cambridge, England). 51: 2690-3. PMID 25575249 DOI: 10.1039/C4Cc09308A  0.792
2015 McDonald BR, Nibbs AE, Scheidt KA. A biomimetic strategy to access the silybins: total synthesis of (-)-isosilybin A. Organic Letters. 17: 98-101. PMID 25517432 DOI: 10.1021/Ol503303W  0.805
2015 Lombardo VM, Dhulst EA, Leitsch EK, Wilmot N, Heath WH, Gies AP, Miller MD, Torkelson JM, Scheidt KA. Cooperative catalysis of cyclic carbonate ring opening: Application towards non-isocyanate polyurethane materials European Journal of Organic Chemistry. 2015: 2791-2795. DOI: 10.1002/Ejoc.201500313  0.683
2014 Zeng BS, Yu X, Siu PW, Scheidt KA. Catalytic enantioselective synthesis of 2-aryl-chromenes. Chemical Science (Royal Society of Chemistry : 2010). 5: 2277-2281. PMID 25705366 DOI: 10.1039/C4Sc00423J  0.69
2014 Liu K, Hovey MT, Scheidt KA. A Cooperative N-Heterocyclic Carbene/Palladium Catalysis System. Chemical Science (Royal Society of Chemistry : 2010). 5: 4026-4031. PMID 25364496 DOI: 10.1039/C4Sc01536C  0.463
2014 Johnston RC, Cohen DT, Eichman CC, Scheidt KA, Cheong PH. Catalytic Kinetic Resolution of a Dynamic Racemate: Highly Stereoselective β-Lactone Formation by N-Heterocyclic Carbene Catalysis. Chemical Science (Royal Society of Chemistry : 2010). 5: 1974-1982. PMID 25045464 DOI: 10.1039/C4Sc00317A  0.824
2014 Hovey MT, Check CT, Sipher AF, Scheidt KA. N-heterocyclic-carbene-catalyzed synthesis of 2-aryl indoles. Angewandte Chemie (International Ed. in English). 53: 9603-7. PMID 25044815 DOI: 10.1002/Anie.201405035  0.484
2014 Lee A, Younai A, Price CK, Izquierdo J, Mishra RK, Scheidt KA. Enantioselective annulations for dihydroquinolones by in situ generation of azolium enolates. Journal of the American Chemical Society. 136: 10589-92. PMID 25017004 DOI: 10.1021/Ja505880R  0.628
2014 Lee A, Scheidt KA. A cooperative N-heterocyclic carbene/chiral phosphate catalysis system for allenolate annulations. Angewandte Chemie (International Ed. in English). 53: 7594-8. PMID 24895280 DOI: 10.1002/Anie.201403446  0.572
2014 Jang KP, Hutson GE, Johnston RC, McCusker EO, Cheong PH, Scheidt KA. Asymmetric homoenolate additions to acyl phosphonates through rational design of a tailored N-heterocyclic carbene catalyst. Journal of the American Chemical Society. 136: 76-9. PMID 24299299 DOI: 10.1021/Ja410932T  0.805
2013 McCusker EO, Scheidt KA. Enantioselective N-heterocyclic carbene catalyzed annulation reactions with imidazolidinones. Angewandte Chemie (International Ed. in English). 52: 13616-20. PMID 24249661 DOI: 10.1002/Anie.201307292  0.811
2013 Lombardo VM, Thomas CD, Scheidt KA. A tandem isomerization/prins strategy: iridium(III)/Brønsted acid cooperative catalysis. Angewandte Chemie (International Ed. in English). 52: 12910-4. PMID 24218144 DOI: 10.1002/Anie.201306462  0.76
2013 Siu PW, Brown ZJ, Farha OK, Hupp JT, Scheidt KA. A mixed dicarboxylate strut approach to enhancing catalytic activity of a de novo urea derivative of metal-organic framework UiO-67. Chemical Communications (Cambridge, England). 49: 10920-2. PMID 24132049 DOI: 10.1039/C3Cc47177B  0.635
2013 Farmer RL, Scheidt KA. A Concise Enantioselective Synthesis and Cytotoxic Evaluation of the Anticancer Rotenoid Deguelin Enabled by a Tandem Knoevenagel/Conjugate Addition/Decarboxylation Sequence. Chemical Science (Royal Society of Chemistry : 2010). 4: 3304-3309. PMID 24101971 DOI: 10.1039/C3Sc50424G  0.756
2013 Katz MJ, Brown ZJ, Colón YJ, Siu PW, Scheidt KA, Snurr RQ, Hupp JT, Farha OK. A facile synthesis of UiO-66, UiO-67 and their derivatives. Chemical Communications (Cambridge, England). 49: 9449-51. PMID 24008272 DOI: 10.1039/C3Cc46105J  0.665
2013 Izquierdo J, Orue A, Scheidt KA. A dual Lewis base activation strategy for enantioselective carbene-catalyzed annulations. Journal of the American Chemical Society. 135: 10634-7. PMID 23829462 DOI: 10.1021/Ja405833M  0.611
2013 Tenenbaum JM, Morris WJ, Custar DW, Scheidt KA. Exploring prins strategies for the synthesis of okilactomycin Strategies and Tactics in Organic Synthesis. 9: 231-248. DOI: 10.1016/B978-0-08-099362-1.00008-4  0.838
2013 Cardinal-David B, Scheidt KA. Carbene catalysis: Beyond the benzoin and stetter reactions Topics in Organometallic Chemistry. 44: 233-260. DOI: 10.1007/3418-2012-47  0.783
2013 Cohen DT, Eichman CC, Phillips EM, Zarefsky ER, Scheidt KA. Corrigendum: Catalytic Dynamic Kinetic Resolutions with N-Heterocyclic Carbenes: Asymmetric Synthesis of Highly Substituted β-Lactones Angewandte Chemie International Edition. 52: 5203-5203. DOI: 10.1002/Anie.201302333  0.824
2013 Scheidt KA, Phillips EM, Dugal-Tessier J. N-Heterocyclic Carbene-Catalyzed Aldol Desymmetrizations Asymmetric Synthesis Ii: More Methods and Applications. 309-316. DOI: 10.1002/9783527652235.ch39  0.809
2012 Cohen DT, Scheidt KA. Cooperative Lewis acid/N-heterocyclic carbene catalysis. Chemical Science (Royal Society of Chemistry : 2010). 3: 53-57. PMID 26413259 DOI: 10.1039/C1Sc00621E  0.626
2012 Izquierdo J, Hutson GE, Cohen DT, Scheidt KA. A continuum of progress: applications of N-hetereocyclic carbene catalysis in total synthesis. Angewandte Chemie (International Ed. in English). 51: 11686-98. PMID 23074146 DOI: 10.1002/Anie.201203704  0.834
2012 Nibbs AE, Scheidt KA. Asymmetric Methods for the Synthesis of Flavanones, Chromanones, and Azaflavanones. European Journal of Organic Chemistry. 2012: 449-462. PMID 22876166 DOI: 10.1002/Ejoc.201101228  0.796
2012 Cui J, Chai DI, Miller C, Hao J, Thomas C, Wang J, Scheidt KA, Kozmin SA. Assembly of four diverse heterocyclic libraries enabled by Prins cyclization, Au-catalyzed enyne cycloisomerization, and automated amide synthesis. The Journal of Organic Chemistry. 77: 7435-70. PMID 22860634 DOI: 10.1021/Jo301061R  0.749
2012 Cohen DT, Eichman CC, Phillips EM, Zarefsky ER, Scheidt KA. Catalytic dynamic kinetic resolutions with N-heterocyclic carbenes: asymmetric synthesis of highly substituted β-lactones. Angewandte Chemie (International Ed. in English). 51: 7309-13. PMID 22700327 DOI: 10.1002/Anie.201203382  0.838
2012 Dugal-Tessier J, O'Bryan EA, Schroeder TB, Cohen DT, Scheidt KA. An N-heterocyclic carbene/Lewis acid strategy for the stereoselective synthesis of spirooxindole lactones. Angewandte Chemie (International Ed. in English). 51: 4963-7. PMID 22489096 DOI: 10.1002/Anie.201201643  0.844
2012 Roberts JM, Fini BM, Sarjeant AA, Farha OK, Hupp JT, Scheidt KA. Urea metal-organic frameworks as effective and size-selective hydrogen-bond catalysts. Journal of the American Chemical Society. 134: 3334-7. PMID 22296523 DOI: 10.1021/Ja2108118  0.354
2012 Xu L, Farmer R, Huang X, Pruell S, Voll E, Pavese J, Valsecchi M, Biddle M, Nibbs A, Avram M, Scheidt KA, Bergan RC. Abstract 4752: Selective inhibition of cancer metastasis with a novel small therapeutic molecule Cancer Research. 72: 4752-4752. DOI: 10.1158/1538-7445.Am2012-4752  0.786
2012 Krishna SN, Luan C, Minasov G, Shuvalova L, Farmer RL, Nibbs A, Scheidt KA, Anderson WF, Bergan RC. Abstract 4751: Structure and inhibition of mitogen-activated protein kinase kinase 4 (MEK4): A prostate cancer pro-invasion protein Cancer Research. 72: 4751-4751. DOI: 10.1158/1538-7445.Am2012-4751  0.782
2012 Brekan JA, Chernyak D, White KL, Scheidt KA. Lewis base-promoted carbon-carbon sp 3-sp 3 coupling reactions of α-silyl silylethers Chemical Science. 3: 1205-1210. DOI: 10.1039/C2Sc00581F  0.819
2012 Cohen DT, Scheidt KA. Cooperative Lewis acid/N-heterocyclic carbene catalysis Chemical Science. 3: 53-57. DOI: 10.1039/c1sc00621e  0.513
2012 Lalonde MB, Farha OK, Scheidt KA, Hupp JT. N -heterocyclic carbene-like catalysis by a metal-organic framework material Acs Catalysis. 2: 1550-1554. DOI: 10.1021/Cs300260F  0.398
2012 Izquierdo J, Hutson GE, Cohen DT, Scheidt KA. Anwendungen der Katalyse mit N-heterocyclischen Carbenen in Totalsynthesen Angewandte Chemie. 124: 11854-11866. DOI: 10.1002/Ange.201203704  0.762
2011 Atienza RL, Roth HS, Scheidt KA. N-heterocyclic carbene-catalyzed rearrangements of vinyl sulfones. Chemical Science (Royal Society of Chemistry : 2010). 2: 1772-1776. PMID 22448316 DOI: 10.1039/C1Sc00194A  0.782
2011 Atienza RL, Scheidt KA. N-Heterocyclic Carbene-Promoted Rauhut]Currier Reactions between Vinyl Sulfones and α,β-Unsaturated Aldehydes. Australian Journal of Chemistry. 64: 1158-1164. PMID 22399824 DOI: 10.1071/Ch11264  0.769
2011 Crane EA, Zabawa TP, Farmer RL, Scheidt KA. Enantioselective synthesis of (-)-exiguolide by iterative stereoselective dioxinone-directed Prins cyclizations. Angewandte Chemie (International Ed. in English). 50: 9112-5. PMID 21932228 DOI: 10.1002/Anie.201102790  0.793
2011 Wang J, Crane EA, Scheidt KA. Highly stereoselective Brønsted acid catalyzed synthesis of spirooxindole pyrans. Organic Letters. 13: 3086-9. PMID 21591768 DOI: 10.1021/Ol200987C  0.833
2011 Tenenbaum JM, Morris WJ, Custar DW, Scheidt KA. Synthesis of (-)-okilactomycin by a Prins-type fragment-assembly strategy. Angewandte Chemie (International Ed. in English). 50: 5892-5. PMID 21560215 DOI: 10.1002/Anie.201102037  0.801
2011 Kleinman SL, Ringe E, Valley N, Wustholz KL, Phillips E, Scheidt KA, Schatz GC, Van Duyne RP. Single-molecule surface-enhanced Raman spectroscopy of crystal violet isotopologues: theory and experiment. Journal of the American Chemical Society. 133: 4115-22. PMID 21348518 DOI: 10.1021/Ja110964D  0.516
2011 Cohen DT, Cardinal-David B, Scheidt KA. Lewis acid activated synthesis of highly substituted cyclopentanes by the N-heterocyclic carbene catalyzed addition of homoenolate equivalents to unsaturated ketoesters. Angewandte Chemie (International Ed. in English). 50: 1678-82. PMID 21308931 DOI: 10.1002/Anie.201005908  0.853
2011 Cohen DT, Cardinal-David B, Roberts JM, Sarjeant AA, Scheidt KA. NHC-catalyzed/titanium(IV)-mediated highly diastereo- and enantioselective dimerization of enals. Organic Letters. 13: 1068-71. PMID 21271734 DOI: 10.1021/Ol103112V  0.829
2011 Xu L, Farmer R, Huang X, Valsecchi M, Pavese J, Voll E, Biddle M, Nibbs A, Pruell S, Avram M, Scheidt K, Bergan RC. Abstract C177: Chemical-driven biological probing: Discovery of a novel antimetastatic drug. Molecular Cancer Therapeutics. 10. DOI: 10.1158/1535-7163.Targ-11-C177  0.785
2011 Atienza RL, Scheidt KA. N-heterocyclic carbene-promoted rauhutcurrier reactions between vinyl sulfones and α,β-unsaturated aldehydes Australian Journal of Chemistry. 64: 1158-1164. DOI: 10.1071/CH11264  0.744
2011 Cohen DT, Cardinal-David B, Roberts JM, Sarjeant AA, Scheidt KA. Titanium-Mediated Diastereo- and Enantioselective Dimerizationof Enals Synfacts. 2011: 665-665. DOI: 10.1055/S-0030-1260366  0.81
2011 Cohen DT, Cardinal-David B, Scheidt KA. NHC-Catalyzed Addition of Homoenolate Equivalents to UnsaturatedKeto Esters Synfacts. 2011: 437-437. DOI: 10.1055/S-0030-1259613  0.839
2011 Farmer RL, Biddle MM, Nibbs AE, Huang X, Xu L, Bergan RC, Scheidt KA. Erratum: Concise syntheses of the abyssinones and discovery of new inhibitors of prostate cancer and MMP-2 expression (ACS Medicinal Chemistry Letters (2010) 1 (400-405) DOI: 10.1021/ml100110x) Acs Medicinal Chemistry Letters. 2. DOI: 10.1021/Ml1003102  0.768
2011 Cohen DT, Cardinal-David B, Scheidt KA. Innentitelbild: Lewis Acid Activated Synthesis of Highly Substituted Cyclopentanes by the N-Heterocyclic Carbene Catalyzed Addition of Homoenolate Equivalents to Unsaturated Ketoesters (Angew. Chem. 7/2011) Angewandte Chemie. 123: 1484-1484. DOI: 10.1002/Ange.201007985  0.838
2010 Farmer RL, Biddle MM, Nibbs AE, Huang X, Bergan RC, Scheidt KA. Concise syntheses of the abyssinones and discovery of new inhibitors of prostate cancer and MMP-2 expression. Acs Medicinal Chemistry Letters. 1: 400-405. PMID 21116437 DOI: 10.1021/Ml100110X  0.798
2010 Crane EA, Scheidt KA. Prins-type macrocyclizations as an efficient ring-closing strategy in natural product synthesis. Angewandte Chemie (International Ed. in English). 49: 8316-26. PMID 20931580 DOI: 10.1002/Anie.201002809  0.806
2010 Phillips EM, Riedrich M, Scheidt KA. N-heterocyclic carbene-catalyzed conjugate additions of alcohols. Journal of the American Chemical Society. 132: 13179-81. PMID 20809579 DOI: 10.1021/Ja1061196  0.814
2010 Raup DE, Cardinal-David B, Holte D, Scheidt KA. Cooperative catalysis by carbenes and Lewis acids in a highly stereoselective route to gamma-lactams. Nature Chemistry. 2: 766-71. PMID 20729898 DOI: 10.1038/Nchem.727  0.834
2010 Scheidt K. Organic chemistry: Amide bonds made in reverse Nature. 465: 1020-1022. PMID 20577201 DOI: 10.1038/4651020A  0.334
2010 Phillips EM, Roberts JM, Scheidt KA. Catalytic enantioselective total syntheses of bakkenolides I, J, and S: application of a carbene-catalyzed desymmetrization. Organic Letters. 12: 2830-3. PMID 20469924 DOI: 10.1021/Ol100938J  0.692
2010 Cardinal-David B, Raup DE, Scheidt KA. Cooperative N-heterocyclic carbene/Lewis acid catalysis for highly stereoselective annulation reactions with homoenolates. Journal of the American Chemical Society. 132: 5345-7. PMID 20345186 DOI: 10.1021/Ja910666N  0.834
2010 Brekan JA, Reynolds TE, Scheidt KA. Enantioselective synthesis of substituted indanones from silyloxyallenes. Journal of the American Chemical Society. 132: 1472-3. PMID 20085317 DOI: 10.1021/Ja909669E  0.832
2010 Xu L, Farmer R, huang x, Pavese J, Voll E, Irene O, Biddle M, Nibbs A, Valsecchi M, Scheidt K, Bergan R. Abstract B58: Discovery of a novel drug KBU2046 that inhibits conversion of human prostate cancer to a metastatic phenotype Cancer Prevention Research. 3. DOI: 10.1158/1940-6207.Prev-10-B58  0.779
2010 Phillips EM, Roberts JM, Scheidt KA. NHC-Catalyzed Desymmetrization in Natural Product Synthesis Synfacts. 2010: 951-951. DOI: 10.1055/S-0030-1257801  0.432
2010 Brekan JA, Reynolds TE, Scheidt KA. Enantioselective Synthesis of Substituted Indanones Synfacts. 2010: 569-569. DOI: 10.1055/S-0029-1219642  0.835
2010 Kawanaka Y, Phillips EM, Scheidt KA. Enantioselective N-Heterocyclic Carbene Catalyzed MannichReaction Synfacts. 2010: 227-227. DOI: 10.1055/S-0029-1219136  0.398
2010 Evans DA, Scheidt KA, Downey CW. ChemInform Abstract: Synthesis of (-)-Epibatidine Cheminform. 33: no-no. DOI: 10.1002/chin.200204220  0.812
2010 Evans DA, Scheidt KA, Johnston JN, Willis MC. ChemInform Abstract: Enantioselective and Diastereoselective Mukaiyama-Michael Reactions Catalyzed by Bis(oxazoline) Copper(II) Complexes. Cheminform. 32: no-no. DOI: 10.1002/chin.200137074  0.721
2010 Scheidt KA, Tasaka A, Bannister TD, Wendt MD, Roush WR. ChemInform Abstract: Total Synthesis of (-)-Bafilomycin A1 (I): Application of Diastereoselective Crotylboration and Methyl Ketone Aldol Reactions. Cheminform. 30: no-no. DOI: 10.1002/chin.199934259  0.49
2010 ROUSH WR, GWALTNEY SLI, CHENG J, SCHEIDT KA, MCKERROW JH, HANSELL E. ChemInform Abstract: Vinyl Sulfonate Esters and Vinyl Sulfonamides: Potent, Irreversible Inhibitors of Cysteine Proteases. Cheminform. 30: no-no. DOI: 10.1002/chin.199909224  0.43
2010 SCHEIDT KA, CHEN H, FOLLOWS BC, CHEMLER SR, COFFEY DS, ROUSH WR. ChemInform Abstract: Tris(dimethylamino)sulfonium Difluorotrimethylsilicate, a Mild Reagent for the Removal of Silicon Protecting Groups. Cheminform. 30: no-no. DOI: 10.1002/chin.199907076  0.639
2010 Crane EA, Scheidt KA. Die Prins-Makrocyclisierung als effiziente Ringschluss-Strategie in der Naturstoffsynthese Angewandte Chemie. 122: 8494-8505. DOI: 10.1002/Ange.201002809  0.711
2009 Mathies AK, Mattson AE, Scheidt KA. Intermolecular Cross-Acyloin Reactions by Fluoride-Promoted Additions of O-Silyl Thiazolium Carbinols. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 2009: 377-383. PMID 21132061 DOI: 10.1055/S-0028-1087555  0.82
2009 Phillips EM, Wadamoto M, Scheidt KA. Synthesis of Enantioenriched α,α-Disubstituted Cyclopentenes Catalyzed by N-Heterocyclic Carbenes. Synthesis. 4: 687-690. PMID 21085623 DOI: 10.1055/S-0028-1083284  0.837
2009 Phillips EM, Chan A, Scheidt KA. Discovering New Reactions with N-Heterocyclic Carbene Catalysis. Aldrichimica Acta. 42: 55-66. PMID 21072130  0.68
2009 Maki BE, Chan A, Phillips EM, Scheidt KA. N-Heterocyclic Carbene-Catalyzed Oxidations. Tetrahedron. 65: 3102-3109. PMID 20161230 DOI: 10.1016/J.Tet.2008.10.033  0.779
2009 Kawanaka Y, Phillips EM, Scheidt KA. N-heterocyclic carbene-catalyzed enantioselective Mannich reactions with alpha-aryloxyacetaldehydes. Journal of the American Chemical Society. 131: 18028-9. PMID 20000857 DOI: 10.1021/Ja9094044  0.816
2009 Custar DW, Zabawa TP, Hines J, Crews CM, Scheidt KA. Total synthesis and structure-activity investigation of the marine natural product neopeltolide. Journal of the American Chemical Society. 131: 12406-14. PMID 19663512 DOI: 10.1021/Ja904604X  0.813
2009 Nibbs AE, Baize AL, Herter RM, Scheidt KA. Catalytic asymmetric alkylation of substituted isoflavanones. Organic Letters. 11: 4010-3. PMID 19658430 DOI: 10.1021/Ol901676F  0.811
2009 Maki BE, Patterson EV, Cramer CJ, Scheidt KA. Impact of solvent polarity on N-heterocyclic carbene-catalyzed beta-protonations of homoenolate equivalents. Organic Letters. 11: 3942-5. PMID 19645427 DOI: 10.1021/Ol901545M  0.628
2009 Lettan RB, Galliford CV, Woodward CC, Scheidt KA. Amide enolate additions to acylsilanes: in situ generation of unusual and stereoselective homoenolate equivalents. Journal of the American Chemical Society. 131: 8805-14. PMID 19505076 DOI: 10.1021/Ja808811U  0.822
2009 Lee J, Farha OK, Roberts J, Scheidt KA, Nguyen ST, Hupp JT. Metal-organic framework materials as catalysts. Chemical Society Reviews. 38: 1450-9. PMID 19384447 DOI: 10.1039/B807080F  0.479
2009 Maki BE, Scheidt KA. Single-flask synthesis of N-acylated indoles by catalytic dehydrogenative coupling with primary alcohols. Organic Letters. 11: 1651-4. PMID 19320508 DOI: 10.1021/Ol900306V  0.647
2009 Phillips EM, Wadamoto M, Roth HS, Ott AW, Scheidt KA. NHC-catalyzed reactions of aryloxyacetaldehydes: a domino elimination/conjugate addition/acylation process for the synthesis of substituted coumarins. Organic Letters. 11: 105-8. PMID 19049403 DOI: 10.1021/Ol802448C  0.846
2009 Reynolds TE, Binkley MS, Scheidt KA. Addition to Sulfinylimines via Brook Rearrangement of Hydroxypropargylsilanes Synfacts. 2009: 182-182. DOI: 10.1055/S-0028-1087645  0.649
2009 Stokes GY, Buchbinder AM, Gibbs-Davis JM, Scheidt KA, Geiger FM. Chemically diverse environmental interfaces and their reactions with ozone studied by sum frequency generation Vibrational Spectroscopy. 50: 86-98. DOI: 10.1016/J.Vibspec.2008.08.003  0.578
2009 Reynolds TE, Binkley MS, Scheidt KA. ChemInform Abstract: Highly Selective α-Acylvinyl Anion Additions to Imines. Cheminform. 40. DOI: 10.1002/chin.200915064  0.581
2009 Phillips EM, Chan A, Scheidt KA. Discovering new reactions with N-heterocyclic carbene catalysis Aldrichimica Acta. 42: 55-66.  0.68
2008 Maki BE, Chan A, Scheidt KA. Protonation of Homoenolate Equivalents Generated by N-Heterocyclic Carbenes. Synthesis. 2008: 1306-1315. PMID 22347730 DOI: 10.1055/S-2008-1072516  0.72
2008 Gibbs-Davis JM, Kruk JJ, Konek CT, Scheidt KA, Geiger FM. Jammed acid-base reactions at interfaces. Journal of the American Chemical Society. 130: 15444-7. PMID 19006409 DOI: 10.1021/Ja804302S  0.543
2008 Reynolds TE, Binkley MS, Scheidt KA. Highly selective alpha-acylvinyl anion additions to imines. Organic Letters. 10: 5227-30. PMID 18959427 DOI: 10.1021/Ol802227T  0.644
2008 Stokes GY, Buchbinder AM, Gibbs-Davis JM, Scheidt KA, Geiger FM. Heterogeneous ozone oxidation reactions of 1-pentene, cyclopentene, cyclohexene, and a menthenol derivative studied by sum frequency generation. The Journal of Physical Chemistry. A. 112: 11688-98. PMID 18942815 DOI: 10.1021/Jp803277S  0.587
2008 Maki BE, Scheidt KA. N-heterocyclic carbene-catalyzed oxidation of unactivated aldehydes to esters. Organic Letters. 10: 4331-4. PMID 18759433 DOI: 10.1021/Ol8018488  0.641
2008 Reynolds TE, Binkley MS, Scheidt KA. Lewis acid-catalyzed conjugate additions of silyloxyallenes: a selective solution to the intermolecular Rauhut-Currier problem. Organic Letters. 10: 2449-52. PMID 18476709 DOI: 10.1021/Ol800745Q  0.693
2008 Galliford CV, Scheidt KA. An unusual dianion equivalent from acylsilanes for the synthesis of substituted beta-keto esters. Chemical Communications (Cambridge, England). 1926-8. PMID 18401521 DOI: 10.1039/B801597J  0.804
2008 Lettan RB, Woodward CC, Scheidt KA. Highly stereoselective synthesis of substituted gamma-lactams from acylsilanes. Angewandte Chemie (International Ed. in English). 47: 2294-7. PMID 18270992 DOI: 10.1002/Anie.200705229  0.828
2008 Chan A, Scheidt KA. Direct amination of homoenolates catalyzed by N-heterocyclic carbenes. Journal of the American Chemical Society. 130: 2740-1. PMID 18260665 DOI: 10.1021/Ja711130P  0.615
2008 Phillips EM, Reynolds TE, Scheidt KA. Highly diastereo- and enantioselective additions of homoenolates to nitrones catalyzed by N-heterocyclic carbenes. Journal of the American Chemical Society. 130: 2416-7. PMID 18232690 DOI: 10.1021/Ja710521M  0.77
2008 Handa M, Scheidt KA, Bossart M, Zheng N, Roush WR. Studies on the synthesis of apoptolidin A. 1. Synthesis of the C(1)-C(11) fragment. The Journal of Organic Chemistry. 73: 1031-5. PMID 18163645 DOI: 10.1021/Jo702250Z  0.713
2008 Custar DW, Zabawa TP, Scheidt KA. Total synthesis and structural revision of the marine macrolide neopeltolide. Journal of the American Chemical Society. 130: 804-5. PMID 18161979 DOI: 10.1021/Ja710080Q  0.813
2008 Scheidt K, Custar D, Zabawa T. Synthesis of Neopeltolide Synfacts. 2008: 0677-0677. DOI: 10.1055/S-2008-1077862  0.809
2008 Lettan RBI, Woodward CC, Scheidt KA. ChemInform Abstract: Highly Stereoselective Synthesis of Substituted γ-Lactams from Acylsilanes. Cheminform. 39. DOI: 10.1002/chin.200829109  0.366
2008 Handa M, Scheidt KA, Bossart M, Zheng N, Roush WR. ChemInform Abstract: Studies on the Synthesis of Apoptolidin A (I). Part 1. Synthesis of the C(1)-C(11) Fragment. Cheminform. 39. DOI: 10.1002/chin.200822211  0.617
2007 Dieringer JA, Lettan RB, Scheidt KA, Van Duyne RP. A frequency domain existence proof of single-molecule surface-enhanced Raman spectroscopy. Journal of the American Chemical Society. 129: 16249-56. PMID 18052068 DOI: 10.1021/Ja077243C  0.757
2007 Galliford CV, Scheidt KA. Pyrrolidinyl-spirooxindole natural products as inspirations for the development of potential therapeutic agents. Angewandte Chemie (International Ed. in English). 46: 8748-58. PMID 17943924 DOI: 10.1002/Anie.200701342  0.775
2007 Reynolds TE, Scheidt KA. Catalytic enantioselective alpha-acylvinyl anion reactions of silyloxyallenes. Angewandte Chemie (International Ed. in English). 46: 7806-9. PMID 17849415 DOI: 10.1002/Anie.200702818  0.74
2007 Wadamoto M, Phillips EM, Reynolds TE, Scheidt KA. Enantioselective synthesis of alpha,alpha-disubstituted cyclopentenes by an N-heterocyclic carbene-catalyzed desymmetrization of 1,3-diketones. Journal of the American Chemical Society. 129: 10098-9. PMID 17663558 DOI: 10.1021/Ja073987E  0.832
2007 Evans DA, Fandrick KR, Song HJ, Scheidt KA, Xu R. Enantioselective Friedel-Crafts alkylations catalyzed by bis(oxazolinyl)pyridine-scandium(III) triflate complexes. Journal of the American Chemical Society. 129: 10029-41. PMID 17658808 DOI: 10.1021/Ja072976I  0.777
2007 Reynolds TE, Stern CA, Scheidt KA. N-heterocyclic carbene-initiated alpha-acylvinyl anion reactivity: additions of alpha-hydroxypropargylsilanes to aldehydes. Organic Letters. 9: 2581-4. PMID 17539656 DOI: 10.1021/Ol0710515  0.652
2007 Gibbs-Davis JM, Hayes PL, Scheidt KA, Geiger FM. Anion chelation by amido acid functionalized fused quartz/water interfaces studied by nonlinear optics. Journal of the American Chemical Society. 129: 7175-84. PMID 17497776 DOI: 10.1021/Ja068117W  0.536
2007 Milgram BC, Eskildsen K, Richter SM, Scheidt WR, Scheidt KA. Microwave-assisted Piloty-Robinson synthesis of 3,4-disubstituted pyrroles. The Journal of Organic Chemistry. 72: 3941-4. PMID 17432915 DOI: 10.1021/Jo070389+  0.497
2007 Chan A, Scheidt KA. Highly stereoselective formal [3 + 3] cycloaddition of enals and azomethine imines catalyzed by N-heterocyclic carbenes. Journal of the American Chemical Society. 129: 5334-5. PMID 17407298 DOI: 10.1021/Ja0709167  0.637
2007 Mattson AE, Scheidt KA. Nucleophilic acylation of o-quinone methides: an umpolung strategy for the synthesis of alpha-aryl ketones and benzofurans. Journal of the American Chemical Society. 129: 4508-9. PMID 17378561 DOI: 10.1021/Ja068189N  0.743
2007 Phillips EM, Wadamoto M, Chan A, Scheidt KA. A highly enantioselective intramolecular Michael reaction catalyzed by N-heterocyclic carbenes. Angewandte Chemie (International Ed. in English). 46: 3107-10. PMID 17366506 DOI: 10.1002/Anie.200605235  0.835
2007 Biddle MM, Lin M, Scheidt KA. Catalytic enantioselective synthesis of flavanones and chromanones. Journal of the American Chemical Society. 129: 3830-1. PMID 17348659 DOI: 10.1021/ja070394v  0.666
2007 Galliford CV, Martenson JS, Stern C, Scheidt KA. A highly diastereoselective, catalytic three-component assembly reaction for the synthesis of spiropyrrolidinyloxindoles. Chemical Communications (Cambridge, England). 631-3. PMID 17264914 DOI: 10.1039/B609155E  0.81
2007 Galliford CV, Scheidt KA. Catalytic multicomponent reactions for the synthesis of N-aryl trisubstituted pyrroles. The Journal of Organic Chemistry. 72: 1811-3. PMID 17256992 DOI: 10.1021/Jo0624086  0.829
2007 Maki BE, Chan A, Phillips EM, Scheidt KA. Tandem oxidation of allylic and benzylic alcohols to esters catalyzed by N-heterocyclic carbenes. Organic Letters. 9: 371-4. PMID 17217307 DOI: 10.1021/Ol062940F  0.782
2007 Lettan RB, Milgram BC, Scheidt KA. Synthesis of acylsilanes from morpholine amides. Synthesis of 1-(Dimethyl(phenyl)silyl)propan-1-one Organic Syntheses. 84: 22-31. DOI: 10.15227/orgsyn.084.0022  0.833
2007 Wadamoto M, Phillips EM, Reynolds TE, Scheidt KA. α,α-Disubstituted Cyclopentenes via Desymmetrization of 1,3-Diketones Synfacts. 2007: 1096-1096. DOI: 10.1055/S-2007-969005  0.578
2007 Milgram BC, Eskildsen K, Richter SM, Scheidt WR, Scheidt KA. Symmetric 3,4-Disubstituted Pyrroles via Piloty-Robinson Synthesis Synfacts. 2007: 808-808. DOI: 10.1055/S-2007-968799  0.445
2007 Scheidt K, Chan A. N-Heterocyclic Carbene Catalyzed Formal [3+3] Cycloaddition Synfacts. 2007: 0759-0759. DOI: 10.1055/s-2007-968627  0.521
2007 Scheidt K, Galliford C. Rh-Catalyzed Synthesis of N-Aryl Trisubstituted Pyrroles Synfacts. 2007: 0474-0474. DOI: 10.1055/s-2007-968470  0.805
2007 Scheidt K, Galliford C, Martenson J, Stern C. Spirooxindoles from a 3-CR of Imines, Diazoesters, and Olefin Dipolarophiles Synfacts. 2007: 0361-0361. DOI: 10.1055/S-2007-968374  0.736
2007 Scheidt K, Reynolds T, Bharadwaj A. Stereoselective α-Acylvinyl Additions Using Lewis Acids Synfacts. 2007: 0293-0293. DOI: 10.1055/S-2007-968268  0.617
2007 Scheidt K, II R, Reynolds T, Galliford C. Synthesis of Tertiary β-Hydroxy Amides via Acylsilanes Synfacts. 2007: 0303-0303. DOI: 10.1055/S-2007-968180  0.802
2007 Voges AB, Stokes GY, Gibbs-Davis JM, Lettan RB, Bertin PA, Pike RC, Nguyen ST, Scheidt KA, Geiger FM. Insights into heterogeneous atmospheric oxidation chemistry: Development of a tailor-made synthetic model for studying tropospheric surface chemistry Journal of Physical Chemistry C. 111: 1567-1578. DOI: 10.1021/Jp065277L  0.79
2007 Reynolds TE, Stern CA, Scheidt KA. N-Heterocyclic Carbene-Initiated α-Acylvinyl Anion Reactivity: Additions of α-Hydroxypropargylsilanes to Aldehydes. Cheminform. 38. DOI: 10.1002/chin.200743075  0.583
2007 Reynolds TE, Bharadwaj AR, Scheidt KA. Stereoselective Lewis Acid Catalyzed α-Acylvinyl Additions. Cheminform. 38. DOI: 10.1002/chin.200715027  0.604
2007 Galliford C, Scheidt K. Natürliche Pyrrolidinylspirooxindole als Vorlagen für die Entwicklung medizinischer Wirkstoffe Angewandte Chemie. 119: 8902-8912. DOI: 10.1002/Ange.200701342  0.724
2006 Lettan RB, Reynolds TE, Galliford CV, Scheidt KA. Synthesis of tertiary beta-hydroxy amides by enolate additions to acylsilanes. Journal of the American Chemical Society. 128: 15566-7. PMID 17147347 DOI: 10.1021/Ja065605V  0.801
2006 Reynolds TE, Bharadwaj AR, Scheidt KA. Stereoselective Lewis acid-catalyzed alpha-acylvinyl additions. Journal of the American Chemical Society. 128: 15382-3. PMID 17131998 DOI: 10.1021/Ja0653674  0.772
2006 Mattson AE, Bharadwaj AR, Zuhl AM, Scheidt KA. Thiazolium-catalyzed additions of acylsilanes: a general strategy for acyl anion addition reactions. The Journal of Organic Chemistry. 71: 5715-24. PMID 16839153 DOI: 10.1021/Jo060699C  0.81
2006 Mattson AE, Zuhl AM, Reynolds TE, Scheidt KA. Direct nucleophilic acylation of nitroalkenes promoted by a fluoride anion/thiourea combination. Journal of the American Chemical Society. 128: 4932-3. PMID 16608309 DOI: 10.1021/Ja056565I  0.821
2006 Chan A, Scheidt KA. Hydroacylation of activated ketones catalyzed by N-heterocyclic carbenes. Journal of the American Chemical Society. 128: 4558-9. PMID 16594677 DOI: 10.1055/S-2006-941790  0.654
2006 Graves CR, Scheidt KA, Nguyen ST. Enantioselective MSPV reduction of ketimines using 2-propanol and (BINOL)Al(III). Organic Letters. 8: 1229-32. PMID 16524310 DOI: 10.1021/Ol060110W  0.575
2006 Scheidt K, Mattson A, Zuhl A, Reynolds T. Direct Nucleophilic Acylation of Nitroalkenes Synfacts. 2006: 0616-0616. DOI: 10.1055/S-2006-941785  0.777
2006 Scheidt K, Nguyen S, Graves C. Highly Enantioselective Meerwein-Schmidt-Ponndorf-Verley Reduction of Ketimines Synfacts. 2006: 0461-0461. DOI: 10.1055/s-2006-934359  0.522
2006 Lettan RB, Milgram BC, Scheidt KA. Synthesis of Acylsilanes from Morpholine Amides. Synthesis of 1‐(Dimethyl(phenyl)silyl)propan‐1‐One Organic Syntheses. 22-31. DOI: 10.1002/0471264229.Os084.03  0.835
2005 Myers MC, Bharadwaj AR, Milgram BC, Scheidt KA. Catalytic conjugate additions of carbonyl anions under neutral aqueous conditions. Journal of the American Chemical Society. 127: 14675-80. PMID 16231921 DOI: 10.1021/Ja0520161  0.646
2005 Lettan Ii RB, Scheidt KA. Lewis base-catalyzed additions of alkynes using trialkoxysilylalkynes. Organic Letters. 7: 3227-30. PMID 16018627 DOI: 10.1021/Ol051030F  0.506
2005 Ballweg DM, Miller RC, Gray DL, Scheidt KA. Stereoselective synthesis of alpha-silylamines by the direct addition of silyl anions to activated imines. Organic Letters. 7: 1403-6. PMID 15787517 DOI: 10.1021/Ol050244U  0.469
2005 Morris WJ, Custar DW, Scheidt KA. Stereoselective synthesis of tetrahydropyran-4-ones from dioxinones catalyzed by scandium(III) triflate. Organic Letters. 7: 1113-6. PMID 15760152 DOI: 10.1021/Ol050093V  0.837
2005 Chan A, Scheidt KA. Conversion of alpha,beta-unsaturated aldehydes into saturated esters: an Umpolung reaction catalyzed by nucleophilic carbenes. Organic Letters. 7: 905-8. PMID 15727471 DOI: 10.1021/Ol050100F  0.594
2005 Chernick ET, Ahrens MJ, Scheidt KA, Wasielewski MR. Copper-promoted N-arylations of cyclic imides within six-membered rings: a facile route to arylene-based organic materials. The Journal of Organic Chemistry. 70: 1486-9. PMID 15704992 DOI: 10.1021/Jo0481351  0.445
2005 Morris WJ, Custar DW, Scheidt KA. Scandium(III) Triflate-Catalyzed Stereoselec­-tive Synthesis of Tetrahydropyran-4-ones Synfacts. 2005: 60-60. DOI: 10.1055/S-2005-869941  0.452
2004 Mattson AE, Scheidt KA. Catalytic additions of acylsilanes to imines: an acyl anion strategy for the direct synthesis of alpha-amino ketones. Organic Letters. 6: 4363-6. PMID 15524484 DOI: 10.1021/Ol0481129  0.749
2004 Clark CT, Milgram BC, Scheidt KA. Efficient synthesis of acylsilanes using morpholine amides. Organic Letters. 6: 3977-80. PMID 15496078 DOI: 10.1021/Ol0483854  0.48
2004 Bharadwaj AR, Scheidt KA. Catalytic multicomponent synthesis of highly substituted pyrroles utilizing a one-pot sila-Stetter/Paal-Knorr strategy. Organic Letters. 6: 2465-8. PMID 15228305 DOI: 10.1021/Ol049044T  0.688
2004 Mattson AE, Bharadwaj AR, Scheidt KA. The thiazolium-catalyzed Sila-Stetter reaction: conjugate addition of acylsilanes to unsaturated esters and ketones. Journal of the American Chemical Society. 126: 2314-5. PMID 14982429 DOI: 10.1021/Ja0318380  0.799
2004 Clark CT, Lake JF, Scheidt KA. Copper(I)-catalyzed disilylation of alkylidene malonates employing a Lewis base activation strategy. Journal of the American Chemical Society. 126: 84-5. PMID 14709071 DOI: 10.1021/Ja038530T  0.331
2004 Mattson AE, Scheidt KA. Catalytic additions of acylsilanes to imines: An acyl anion strategy for the direct synthesis of α-amino ketones Organic Letters. 6: 4363-4366.  0.717
2003 Galliford CV, Beenen MA, Nguyen ST, Scheidt KA. Catalytic, three-component assembly reaction for the synthesis of pyrrolidines. Organic Letters. 5: 3487-90. PMID 12967306 DOI: 10.1021/Ol035292Y  0.832
2003 Evans DA, Scheidt KA, Fandrick KR, Lam HW, Wu J. Enantioselective indole Friedel--Crafts alkylations catalyzed by bis(oxazolinyl)pyridine-scandium(III) triflate complexes. Journal of the American Chemical Society. 125: 10780-1. PMID 12952445 DOI: 10.1021/ja036985c  0.838
2002 Evans DA, Borg G, Scheidt KA. Remarkably stable tetrahedral intermediates: carbinols from nucleophilic additions to N-acylpyrroles. Angewandte Chemie (International Ed. in English). 41: 3188-91. PMID 12207385 DOI: 10.1002/1521-3773(20020902)41:17<3188::Aid-Anie3188>3.0.Co;2-H  0.734
2002 Scheidt KA, Bannister TD, Tasaka A, Wendt MD, Savall BM, Fegley GJ, Roush WR. Total synthesis of (-)-bafilomycin A(1). Journal of the American Chemical Society. 124: 6981-90. PMID 12059221 DOI: 10.1021/Ja017885E  0.842
2002 Roush WR, Bannister TD, Wendt MD, VanNieuwenhze MS, Gustin DJ, Dilley GJ, Lane GC, Scheidt KA, Smith WJ. An NMR method for assigning relative stereochemistry to beta-hydroxy ketones deriving from aldol reactions of methyl ketones. The Journal of Organic Chemistry. 67: 4284-9. PMID 12054964 DOI: 10.1021/Jo0164148  0.801
2002 Roush WR, Bannister TD, Wendt MD, Jablonowski JA, Scheidt KA. Studies on the synthesis of bafilomycin A(1): stereochemical aspects of the fragment assembly aldol reaction for construction of the C(13)-C25) segment. The Journal of Organic Chemistry. 67: 4275-83. PMID 12054963 DOI: 10.1021/Jo016413F  0.742
2001 Evans DA, Scheidt KA, Downey CW. Synthesis of (-)-epibatidine. Organic Letters. 3: 3009-12. PMID 11554830 DOI: 10.1021/Ol016420Q  0.845
2001 Evans DA, Scheidt KA, Johnston JN, Willis MC. Enantioselective and diastereoselective Mukaiyama-Michael reactions catalyzed by bis(oxazoline) copper(II) complexes. Journal of the American Chemical Society. 123: 4480-91. PMID 11457234 DOI: 10.1021/Ja010302G  0.77
1999 Scheidt KA, Tasaka A, Bannister TD, Wendt MD, Roush WR. Total Synthesis of (-)-Bafilomycin A : Application of Diastereoselective Crotylboration and Methyl Ketone Aldol Reactions. Angewandte Chemie (International Ed. in English). 38: 1652-1655. PMID 29710989 DOI: 10.1002/(Sici)1521-3773(19990601)38:11<1652::Aid-Anie1652>3.0.Co;2-K  0.764
1999 Scheidt KA, Tasaka A, Bannister TD, Wendt MD, Roush WR. Totalsynthese von (−)-Bafilomycin A1: Anwendung von diastereoselektiver Crotylborierung und Methylketon-Aldolreaktionen Angewandte Chemie. 111: 1760-1762. DOI: 10.1002/(Sici)1521-3757(19990601)111:11<1760::Aid-Ange1760>3.0.Co;2-A  0.396
1998 Scheidt KA, Roush WR, McKerrow JH, Selzer PM, Hansell E, Rosenthal PJ. Structure-based design, synthesis and evaluation of conformationally constrained cysteine protease inhibitors. Bioorganic & Medicinal Chemistry. 6: 2477-94. PMID 9925304 DOI: 10.1016/S0968-0896(98)80022-9  0.468
1998 Ley SV, Osborn HMI, Priepke HWM, Warriner SL, Scheidt KA, Roush WR. (1'S, 2'S)-Methyl-30,40-(1', 2' -Dimethoxycyclohexane-1', 2'-Diyl)-Alpha -D-Mannopyranoside : (Alpha -D-Mannopyranoside, Methyl 3,4-O-(1,2-Dimethoxy-1 ,2 -Cyclohexanediyl)-, 3S(S)-) Organic Syntheses. 75: 170-176. DOI: 10.15227/Orgsyn.075.0170  0.414
1998 Scheidt KA, Chen H, Follows BC, Chemler SR, Coffey DS, Roush WR. Tris(dimethylamino)sulfonium Difluorotrimethylsilicate, a Mild Reagent for the Removal of Silicon Protecting Groups The Journal of Organic Chemistry. 63: 6436-6437. DOI: 10.1021/Jo981215I  0.696
1998 Roush WR, Gwaltney SL, Cheng J, Scheidt KA, McKerrow JH, Hansell E. Vinyl sulfonate esters and vinyl sulfonamides: Potent, irreversible inhibitors of cysteine proteases [10] Journal of the American Chemical Society. 120: 10994-10995. DOI: 10.1021/Ja981792O  0.489
1998 Scheidt KA, Xu Z, Roush WR, Johannes CW, Houri AF, La DS, Cogan DA, Hofilena GE, Hoveyda AH. Applications of Zr-catalyzed carbomagnesation and Mo-catalyzed macrocyclic ring closing metathesis in asymmetric synthesis. Enantioselective synthesis of Sch 38516 (Fluvirucin B1) Chemtracts. 11: 522-530.  0.347
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