Cooperative Lewis Acid/N-Heterocyclic Carbene Catalysis
Cohen, D. T.; Scheidt, K. A.
Chem. Sci. 2012, 3, 53-57.
Single-Molecule Tip-Enhanced Raman Spectroscopy
Sonntag, M. D.; Klingsporn, J. M.; Garibay, L. J.; Roberts, J. M.; Dieringer, J. A.; Seideman, T.; Scheidt, K. A.; Jensen, L.; Schatz, G. C.; Van Duyne, R. P.
J. Phys. Chem. C. 2012, 116, 478-483.
Two Azolium Rings are Better than One: A Strategy for Controlling Catenation and Morphology in Zn and Cu Metal-Organic Frameworks
Roberts, J. M.; Farha, O. K.; Sarjeant, A. A.; Hupp, J. T.; Scheidt, K. A.
Cryst. Growth Des. 2011, 11, 4747-4750.
(S)-5-Benzyl-2-mesityl-6,6-dimethyl-6,8-dihydro-5H-[1,2,4]triazolo[3,4-C][1,4]oxazin-2-ium tetrafluoroborate
Eichman, C. C.; Cohen, D. T.; Scheidt, K. A.
The Electronic Encyclopedia of Reagents for Organic Synthesis, 2011.
N-Heterocyclic Carbene-Promoted Rauhut-Currier Reactions between Vinyl Sulfones and α,β-Unsaturated Aldehydes
Atienza, R. L.; Scheidt, K. A.Aust. J. Chem. 2011, 64, 1158-1164.
Enantioselective Synthesis of (–)-Exiguolide by Iterative Stereoselective Dioxinone-Directed Prins Cyclizations
Crane, E. A.; Zabawa, T. P.; Farmer, R. L. Scheidt, K. A.
Angew. Chem. Int. Ed. 2011, 50, 9112-9115.
N-Heterocyclic Carbene-Catalyzed Rearrangements of Vinyl Sulfones
Atienza, R. L.; Roth, H. R.; Scheidt, K. A.
Chem. Sci. 2011, 2, 1772-1776
Highly Stereoselective Brønsted Acid Catalyzed Synthesis of Spirooxindole Pyrans
Wang, J.; Crane, E. A.; Scheidt, K. A.
Org. Lett. 2011, 13, 3086-3089.
Synthesis of (–)-Okilactomycin by a Prins-Type Fragment-Assembly Strategy
Tenenbaum, J. M.; Morris, W. J.; Custar, D. W.; Scheidt, K. A.
Angew. Chem. Int. Ed. 2011, 50, 5892-5895.
Single-Molecule Surface-Enhanced Raman Spectroscopy of Crystal Violet Isotopologues: Theory and Experiment
Kleinman, S. L.; Ringe, E.; Valley, N.; Wustholz, K. L.; Phillips, E. M.; Scheidt, K. A.; Schatz, G. C.; Van Duyne, R. V.
J. Am. Chem. Soc. 2011, 133, 4115-4122.
NHC-Catalyzed/Titanium(IV)–Mediated Highly Diastereo- and Enantioselective Dimerization of Enals
Cohen, D.; Cardinal-David, B.; Roberts, J. M.; Sarjeant, A. A.; Scheidt, K. A.
Org. Lett. 2011, 13, 1068-1071.
Lewis Acid Activated Synthesis of Highly Substituted Cyclopentanes by the N-Heterocyclic Carbene Catalyzed Addition of Homoenolate Equivalents to Unsaturated Ketoesters
Cohen, D.; Cardinal-David, B.; Scheidt, K. A.
Angew. Chem. Int. Ed. 2011, 50, 1678-1682.
N-Heterocyclic Carbene-Catalyzed Conjugate Additions of Alcohols
Phillips, E. M.; Riedrich, M.; Scheidt, K. A.
J. Am. Chem. Soc. 2010, 132, 13179–13181.
Prins-Type Macrocyclizations as an Efficient Ring-Closing Strategy in Natural Product Synthesis
Crane, E. A.; Scheidt, K. A.
Angew. Chem. Int. Ed. 2010, 49, 8316 – 8326.
Concise Syntheses of the Abyssinones and Discovery of New Inhibitors of Prostate Cancer and MMP-2 Expression
Farmer, R. L.; Biddle, M. M.; Nibbs, A. E.; Huang, X.; Bergan, R. C.; Scheidt, K. A.
ACS Med. Chem. Lett. 2010, 1, 400–405.
Amide Bonds Made in Reverse
Scheidt, K. A.
Nature News and Views 2010, 465, 1020–1022.
Cooperative N-Heterocyclic Carbene/Lewis Acid Catalysis for Highly Stereoselective Annulation Reactions with Homoenolates
Cardinal-David, B.; Raup, D. E. A; Scheidt, K. A.
J. Am. Chem. Soc. 2010, 132, 5345–5347.
Catalytic Enantioselective Total Syntheses of Bakkenolides I, J, and S: Application of a Carbene-Catalyzed Desymmetrization
Phillips, E. M.; Roberts, J. M.; Scheidt, K. A.
Org. Lett. 2010, 12, 2830–2833.
Cooperative Catalysis by Carbenes and Lewis Acids in a Highly Stereoselective Route to γ-Lactams
Raup, D. E. A.; Cardinal-David, B.; Holte, D.; Scheidt, K. A.
Nat. Chem. 2010, 2, 766-771.
Enantioselective Synthesis of Substituted Indanones from Silyloxyallenes
Brekan, J. A.; Reynolds, T. E; Scheidt, K. A.
J. Am. Chem. Soc. 2010, 132, 1472-1473.
Discovering New Reactions with N-Heterocyclic Carbene Catalysis
Phillips, E. M.; Chan, A.; Scheidt, K. A.
Aldrichimica Acta 2009, 42, 55-66.
N-Heterocyclic Carbene-Catalyzed Enantioselective Mannich Reactions with α-Aryloxyacetaldehydes
Kawanaka, Y.; Phillips, E. M.; Scheidt, K. A.
J. Am. Chem. Soc. 2009, 131, 18028-18029.
Catalytic Asymmetric Alkylation of Substituted Isoflavanones
Nibbs, A. E.; Maize, A. L.; Herter, R. M.; Scheidt, K. A.
Org. Lett. 2009, 11, 4010-4013.
Synthesis and Gas Sorption Properties of a Metal-Azolium Framework (MAF) Material
Lee, J. Y.; Roberts, J. M.; Farha, O. K.; Sarjeant, A. A.; Scheidt, K. A.; Hupp, J. T.
Inorg. Chem. 2009, 48, 9971-9973
Impact of Solvent Polarity on N-Heterocyclic Carbene-Catalyzed β-Protonations of Homoenolate Equivalents
Maki, B. E.; Patterson, E. V.; Cramer, C. J.; Scheidt, K. A.
Org. Lett. 2009, 48, 3942-3945.
Total Synthesis and Structure-Activity Investigation of the Marine Natural Product Neopeltolide
Custar, D. W.; Zabawa, T. P.; Hines, J.; Crews, C. M.; Scheidt, K. A.
J. Am. Chem. Soc. 2009, 131, 12406-12414.
Amide Enolate Additions to Acylsilanes: In Situ Generation of Unusual and Stereoselective Homoenolate Equivalents
Lettan, R. B., II; Galliford, C. V.; Woodward, C. C.; Scheidt, K. A.
J. Am. Chem. Soc. 2009, 131, 8805-8814.
Metal-Organic Framework Materials as Catalysts
Lee, J. Y.; Farha, O. K.; Roberts, J. T; Scheidt, K. A.; Nguyen, S. T.; Hupp, J. T.
Chem. Soc. Rev. 2009, 38, 1450-1459.
MEK4 Function, Genistein Treatment, and Invasion of Human Prostate Cancer Cells
Xu, L.; Ding, Y.; Catalona, W. J.; Yang, X. J.; Anderson, W. F.; Jovanovic, B.; Wellman, K.; Kilmer, J.; Huang, X.; Scheidt, K. A.; Montgomery, R. B.; Bergan, R. C.
J. Nat. Can. Inst. 2009, 101, 1141-1155.
Single-Flask Synthesis of N-Acylated Indoles by Catalytic Dehydrogenative Coupling with Primary Alcohols
Maki, B. E.; Scheidt, K. A.
Org. Lett. 2009, 11, 1651-1654.
NHC-Catalyzed Reactions of Aryloxyacetaldehydes: A Domino Elimination/Conjugate Addition/Acylation Process for the Synthesis of Substituted Coumarins
Phillips, E. M.; Wadamoto, M.; Roth, H. S.; Ott, A. W.; Scheidt, K. A.
Org. Lett. 2009, 11, 105-108.
Intermolecular Crossed-Acyloin Reactions by Fluoride-Promoted Additions of O-Silyl Thiazolium Carbinols
Mathies, A. K.; Mattson, A. E.; Scheidt, K. A.
Synlett, Invited Contribution to Special Edition For Journal Awardees, 2009, 2009, 377-383.
Synthesis of Enantioenriched α,α-Disubstituted Cyclopentenes Catalyzed by N-Heterocyclic Carbenes
Phillips, E. M.; Wadamoto, M.; Scheidt, K. A.
Synthesis, Invited PSP article, 2009, 687-690.
N-Heterocyclic Carbene-Catalyzed Oxidations
Maki, B. E.; Chan, A.; Phillips, E. M.; Scheidt, K. A.
Tetrahedron, invited article for special Justin DuBois Issue, 2009, 65, 3102-3109.
Highly Selective α-Acylvinyl Anion Additions to Imines
Reynolds, T. E.; Binkley, M. S.; Scheidt, K. A.
Org. Lett. 2008, 10, 5227-5230
Jammed Acid-Base Reactions at Interfaces
Gibbs-Davis, J. M.; Kruk, J. J.; Konek, C. T.; Scheidt, K. A.; Geiger, F. M.
J. Am. Chem. Soc. 2008, 130, 15444-15447.
Heterogeneous Ozone Oxidation Reactions of 1-Pentene, Cyclopentene, Cyclohexene, and a Menthenol Derivative Studied by Sum Frequency Generation
Stokes, G. Y.; Buchbinder, A. M.; Gibbs-Davis, J. M.; Scheidt, K. A.; Geiger, F. M.
J. Phys. Chem. A. 2008, 112, 11688-11698.
N-Heterocyclic Carbene-Catalyzed Oxidation of Unactivated Aldehydes to Esters
Maki, B. E. and Scheidt, K. A.
Org. Lett. 2008, 10, 4331-4334.
Lewis Acid-Catalyzed Conjugate Additions of Silyloxyallenes: A Selective Solution to the Intermolecular Rauhut−Currier Problem
Reynolds, T. E.; Binkley, M. S.; Scheidt, K. A.
Org. Lett. 2008, 10, 2449–2452.
Protonation of Homoenolate Equivalents Generated by N-Heterocyclic Carbenes
Maki, B. E.; Chan, A.; Scheidt, K. A.
Synthesis, invited Feature Article, 2008, 8, 1306-1315.
An Unusual Dianion Equivalent from Acylsilanes for the Synthesis of Substituted β-Keto Esters
Galliford, C. V. and Scheidt, K. A.
Chem. Commun. 2008, 16, 1926-1928.
Direct Amination of Homoenolates Catalyzed by N-Heterocyclic Carbenes
Chan. A. and Scheidt, K. A.
J. Am. Chem. Soc. 2008, 130, 2740-2741.
Highly Diastereo- and Enantioselective Additions of Homoenolates to Nitrones Catalyzed by N-Heterocyclic Carbenes
Phillips, E. M.; Reynolds, T. E.; Scheidt, K. A.
J. Am. Chem. Soc. 2008, 130, 2416-2417.
Highly Stereoselective Synthesis of Substituted γ-Lactams From Acylsilanes
Lettan II, R. B.; Woodward, C. C.; Scheidt, K. A.
Angew. Chem. Int. Ed. 2008, 47, 2294-2297.
Total Synthesis and Structural Revision of the Marine Macrolide Neopeltolide
Custar, D. W.; Zabawa, T. P.; Scheidt, K. A.
J. Am. Chem. Soc. 2008, 130, 804-805.
A Frequency Domain Existence Proof of Single-Molecule Surface-Enhanced Raman Spectroscopy
Dieringer, J. A.; Lettan, R. B., II; Scheidt, K. A.; Van Duyne, R. P.
J. Am. Chem. Soc. 2007, 129, 16249-16256.
Catalytic Enantioselective α-Acylvinyl Addition Reactions of Silyloxyallenes
Reynolds, T. E.; Scheidt, K. A.
Angew. Chem Int. Ed. 2007, 46, 7806-7809.
Enantioselective Synthesis of α,α-Disubstituted Cyclopentenes by an N-Heterocyclic Carbene-Catalyzed Desymmetrization of 1,3-Diketones
Wadamoto, M.; Phillips, E.M.; Reynolds, T. E.; Scheidt, K. A.
J. Am. Chem. Soc. 2007, 129, 10098-10099.
5-(1,1-dimethylethyl)-5,6-dihydro-2-phenyl-(5S)-oxazolo[2,3-c]-1,2,4-triazolium tetrafluoroborate
Scheidt, K. A. and Mattson, A. E.
The Electronic Encyclopedia of Reagents for Organic Synthesis, 2007.
N-Heterocyclic Carbene-Initiated α-Acylvinyl Anion Reactivity: Additions of α-Hydroxypropargylsilanes to Aldehydes
Reynolds, T. E.; Stern, C. A.; Scheidt, K. A.
Org. Lett. 2007, 9, 2581-2584.
Pyrrolidinyl-Spirooxindole Natural Products as Inspirations for the Development of Potential Therapeutic Agents
Galliford, C. V.; Scheidt, K. A.
Angew. Chem. Int. Ed. 2007, 46, 8748-8758.
Highly Stereoselective Formal [3+3] Cycloaddition of Enals and Azomethine Imines Catalyzed by N-Heterocyclic Carbenes
Chan, A.; Scheidt, K. A.
J. Am. Chem. Soc. 2007, 129, 5334-5335.
Anion Chelation by Amino Acid-Functionalized Fused Quartz/Water Interfaces Studied by Nonlinear Optics
Gibbs-Davis, J. M.; Hayes, P. L.; Scheidt, K. A.; Geiger, F. M.
J. Am. Chem. Soc. 2007, 129, 7175-7184.
Microwave-Assisted Piloty–Robinson Synthesis of 3,4-Disubstitued Pyrroles
Milgram, B. C.; Eskildsen, K.; Richter, S. M.; Scheidt, W. R.; Scheidt, K. A.
J. Org. Chem. 2007, 72, 3941-3944.
Nucleophilic Acylation of o-Quinone Methides: An Umpolung Strategy for the Synthesis of α-Aryl Ketones and Benzofurans
Mattson, A. E.; Scheidt, K. A.
J. Am. Chem. Soc. 2007, 129, 4508-4509.
Catalytic Enantioselective Synthesis of Flavanones and Chromanones
Biddle, M. A.; Lin, M.; Scheidt, K. A.J. Am. Chem. Soc. 2007, 129, 3830-3831.
Highly Enantioselective Intramolecular Michael Reaction Catalyzed by N-Heterocyclic Carbenes
Phillips, E. M.; Wadamoto, M.; Chan, A.; Scheidt, K. A.
Angew. Chem. Int. Ed. 2007, 46, 3107-3110.
Catalytic Multicomponent Reactions for the Synthesis of N-Aryl Trisubstituted Pyrroles
Galliford, C. V.; Scheidt, K. A.
J. Org. Chem. 2007, 72, 1811-1813.
Environmental Biogeochemistry Studied by Second Harmonic Generation: A Look at the Agricultural Antibiotic Oxytetracycline
Hayes, P. L.; Gibbs-Davis, J. M.; Musorrafiti, M. J.; Mifflin, A. M.; Scheidt, K. A.; Geiger, F. M.
Invited contribution to the Kenneth B. Eisenthal Festschrift in for J. Phys. Chem. C. 2007, 111, 8796-8804.
Tandem Oxidation of Allylic and Benzylic Alcohols to Esters Catalyzed by N-Heterocyclic Carbenes
Maki, B. E.; Chan, A.; Phillips, E. M.; Scheidt, K. A.
Org. Lett. 2007, 9, 371-374.
Synthesis of Acylsilanes from Morpholine Amides. Synthesis of 1-(Dimethyl(Phenyl)silyl)propan-1-one
Lettan, R. B., II; Milgram, B. C.; Scheidt, K. A.
Org. Syn. 2007, 84, 22-31.
Insights into Heterogeneous Atmospheric Oxidation Chemistry: Development of a Tailor-Made Synthetic Model for Studying Tropospheric Surface Chemistry
Voges. A.B.; Yin, G.; Gibbs-Davis, J. M.; Lettan, R. B., II; Bertin, P. A.; Pike, R. C.; Nguyen, S. T.; Scheidt, K. A.; Geiger, F. M.
J. Phys. Chem. C. Feature article, 2007, 111, 1567-1578.
A Highly Diastereoselective, Catalytic Three-Component Assembly Reaction for the Synthesis of Spiropyrrolidinyloxindoles
Galliford, C. V.; Martenson, J. S.; Stern, C. A.; Scheidt, K. A.
Chem. Commun. 2007, 6, 631-633.
Synthesis of Tertiary β-Hydroxy Amides by Enolate Additions to Acylsilanes
Lettan, R. B., II; Reyonlds, T. E.; Galliford, C. V.; Scheidt, K. A.
J. Am. Chem. Soc. 2006, 128, 15566-15567.
Triethoxysilane (Update)
Scheidt, K. A. and Lettan II, R. B.
The Electronic Encyclopedia of Reagents for Organic Synthesis, 2006.
Stereoselective Lewis Acid-Catalyzed α-Acylvinyl Additions
Reynolds, T. E.; Bharadwaj, A. R.; Scheidt, K. A.
J. Am. Chem. Soc. 2006, 128, 15382-15383.
Thiazolium-Catalyzed Additions of Acylsilanes: A General Strategy for Acyl Anion Addition Reactions
Mattson, A. E.; Bharadwaj, A. R.; Zuhl, A. M.; Scheidt, K. A.
J. Org. Chem. 2006, 71, 5715-5724.
Hydroacylation of Activated Ketones Catalyzed by N-Heterocyclic Carbenes
Chan, A.; Scheidt, K. A.
J. Am. Chem. Soc. 2006, 128, 4558-4559.
Direct Nucleophilic Acylation of Nitroalkenes Promoted by a Fluoride Anion/Thiourea Combination
Mattson, A. E.; Zuhl, A. M.; Reynolds, T. E.; Scheidt, K. A.
J. Am. Chem. Soc. 2006, 128, 4932-4933.
Enantioselective MSPV Reduction of Ketimines Using 2-Propanol and (BINOL)AlIII
Graves, C. R.; Scheidt, K. A.; Nguyen, S. T.
Org. Lett. 2006, 8, 1229-1232.
Catalytic Conjugate Additions of Carbonyl Anions under Neutral Aqueous Conditions
Myers, M. C.; Bharadwaj, A. R; Milgram, B. C.; Scheidt, K. A.
J. Am. Chem. Soc. 2005, 127, 14675-14680.
Lewis Base-Catalyzed Additions of Alkynes Using Trialkoxysilylalkynes
Lettan, R. B., II; Scheidt, K. A.
Org. Lett. 2005, 7, 3227-3230.
Stereoselective Synthesis of α-Silylamines by the Direct Addition of Silyl Anions to Activated Imines
Ballweg, D. M.; Miller, R. C.; Gray, D. L; Scheidt, K. A.
Org. Lett. 2005, 7, 1403-1406.
Stereoselective Synthesis of Tetrahydropyran-4-ones from Dioxinones Catalyzed by Scandium(III) Triflate
Morris, W. J.; Custar, D. W.; Scheidt, K. A.
Org. Lett. 2005, 7, 1113-1116.
Copper-Promoted N-Arylations of Cyclic Imides within Six-Membered Rings: A Facile Route to Arylene-Based Organic Materials
Chernick, E. T.; Ahrens, M. J.; Scheidt, K. A.; Wasielewski, M. R.
J. Org. Chem. 2005, 70, 1486-1489.
Conversion of α,β-Unsaturated Aldehydes into Saturated Esters: An Umpolung Reaction Catalyzed by Nucleophilic Carbenes
Chan, A.; Scheidt, K. A.
Org. Lett. 2005, 7, 905-908.
Catalytic Additions of Acylsilanes to Imines: An Acyl Anion Strategy for the Direct Synthesis of α-Amino Ketones
Mattson, A. E.; Scheidt, K. A.
Org. Lett. 2004, 6, 4363-4366.
Efficient Synthesis of Acylsilanes Using Morpholine Amides
Clark, C. T.; Milgram, B. C.; Scheidt, K. A.
Org. Lett. 2004, 6, 3977-3980.
Catalytic Multicomponent Synthesis of Highly Substituted Pyrroles Utilizing a One-Pot Sila-Stetter/Paal–Knorr Strategy
Bharadwaj, A. R.; Scheidt, K. A.
Org. Lett. 2004, 6, 2465-2468.
The Thiazolium-Catalyzed Sila-Stetter Reaction: Conjugate Addition of Acylsilanes to Unsaturated Esters and Ketones
Mattson, A. E.; Bharadwaj, A. R.; Scheidt, K. A.
J. Am. Chem. Soc. 2004, 126, 2314-2315.
Copper(I)-Catalyzed Disilylation of Alkylidene Malonates Employing a Lewis Base Activation Strategy
Clark, C. T.; Lake, J. F.; Scheidt, K. A.
J. Am. Chem. Soc. 2004, 126, 84-85.
Catalytic, Three-Component Assembly Reaction for the Synthesis of Pyrrolidines
Galliford, C. V; Beenen, M. A.; Nguyen, S. T.; Scheidt, K. A.
Org. Lett. 2003, 5, 3487-3490.
Studies on the Synthesis of Apoptolidin A. 1. Synthesis of the C(1)-C(11) Fragment
Handa, M.; Scheidt, K. A.; Bossart, M.; Zheng, N.; Roush, W. R.
J. Org. Chem. 2008, 73, 1031-1035.
Enantioselective Friedel-Crafts Alkylations Catalyzed by Bis(oxazolinyl)pyridine-Scandium(III) Triflate Complexes
Evans, D. A; Fandrick, K. R.; Song, H.-J.; Scheidt, K. A.; Xu, R.
J. Am. Chem. Soc. 2007, 129, 10029-10041.
Enantioselective Indole Friedel-Crafts Alkylations Catalyzed by Bis(oxazolinyl)pyridine-Scandium(III) Triflate Complexes
Evans, D. A.; Scheidt, K. A.; Fandrick, K. R.; Lam, H. W.; Wu, J.
J. Am. Chem. Soc. 2003, 125, 10780-10781.
Remarkably Stable Tetrahedral Intermediates: Carbinols from Nucleophilic Additions to N-Acylpyrroles
Evans, D. A.; Borg, G.; Scheidt, K. A.
Angew. Chem. Int. Ed. 2002, 41, 3188-3191.
Total Synthesis of (-)-Bafilomycin A1
Scheidt, K. A.; Bannister, T. D.; Tasaka, A.; Wendt, M. D.; Savall, B. D.; Fegley, G. J.; Roush, W. R.
J. Am. Chem. Soc. 2002, 124, 6981-6990.
Studies on the Synthesis of Bafilomycin A: Stereochemical Aspects of the Fragment Assembly Aldol Reaction for Construction of the C(13)-C(25) Segment
Roush, W. R.; Bannister, T. D.; Wendt, M. D.; Jablonowski, J. A.; Scheidt, K. A.
J. Org. Chem. 2002, 67, 4275-4283.
An NMR Method for Assigning Relative Stereochemistry to β-Hydroxy Ketones Deriving from Aldol Reactions of Methyl Ketones
Roush, W. R.; Bannister, T. D.; Wendt, M. D.; VanNieuwenhze, M. S.; Gustin, D. J.; Dilley, G. J.; Lane, G. C.; Scheidt, K. A. ; Smith, W. J.
J. Org. Chem. 2002, 67, 4284-4289.
Synthesis of (–)-Epibatidine
Evans, D. A.; Scheidt, K. A.; Downey, C. W.
Org. Lett. 2001, 3, 3009-3012.
Enantioselective and Diastereoselective Mukaiyama-Michael Reactions Catalyzed by Bis(oxazoline) Copper(II) Complexes
Evans, D. A.; Scheidt, K. A.; Johnston, J. N.; Willis, M. C.
J. Am. Chem. Soc. 2001, 123, 4480-4491.
Total Synthesis of (–)-Bafilomycin A1: Application of Diastereoselective Crotylboration and Methyl Ketone Aldol Reactions
Scheidt, K. A.; Tasaka, A.; Bannister, T. D.; Wendt, M. D.; Roush, W. R.
Angew. Chem. Int. Ed. 1999, 38, 1652-1655.
Structure-based design, synthesis and evaluation of conformationally constrained cysteine protease inhibitors
Scheidt, K. A.; Roush, W. R.; McKerrow, J. H.; Selzer, P. M.; Hansell, E.; Rosenthal, P. J.
Bioorg. Med. Chem. 1998, 6, 2477-2494.”
Vinyl Sulfonate Esters and Vinyl Sulfonamides: Potent, Irreversible Inhibitors of Cysteine Proteases
Roush, W. R.; Gwaltney, S. L.; Cheng, J.; Scheidt, K. A.; McKerrow, J. H.; Hansell, E.
J. Am. Chem. Soc. 1998, 120, 10994-10995.
Tris(dimethylamino)sulfonium Difluorotrimethylsilicate, a Mild Reagent for the Removal of Silicon Protecting Groups
Scheidt, K. A.; Chen, H.; Follows, B. C.; Chemler, S. R.; Coffey, D. S.; Roush, W. R.
J. Org. Chem. 1998, 63, 6436-6437.
Applications of Zr-Catalyzed Carbomagnesation and Mo-Catalyzed Macrocyclic Ring Closing Metathesis in Asymmetric Synthesis: Enantioselective Synthesis of Sch38516 (Fluvirucin B1)
Scheidt, K. A.; Roush, W. R.; Houri, A. F.; La, D. S.; Cogan, D. A.; Hofilena, G. E.; Hoveyda, A. H.
Chemtracts 1998, 11, 522-530.”
Design, Syntheses and Studies of New Antibacterial, Antifungal and Antiviral Agents
Miller, M. J.; Darwish, I.; Ghosh, A.; Ghosh, M.; Hansel, J.-G.; Hu, J.; Niu, C.; Ritter, A.; Scheidt, K. A.; Süling, C.; Sun, S.
Anti-Infectives: Recent Advances in Chemistry and Structure-Activity Relationships, Royal Society of Chemistry Special Publication 1997, No. 198, p. 116-138, Cambridge, UK.”