Publications
| 85. |
Borg, G.; Chino , M.; Ellman, J. A. Asymmetric Synthesis of Pre-Protected alpha,alpha-Disubstituted Amino Acids from tert-Butanesulfinyl Ketimines Tetrahedron Lett. 2001, 42, 1433-1436. |
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| 84. |
Owens, T. D.; Hollander, F. J.; Oliver, A. G.; Ellman, J. A. Synthesis, Utility, and Structure of Novel Bis(sulfinyl)imidoamidine Ligands for Asymmetric Lewis Acid Catalysis J. Am. Chem. Soc. 2001, 123, 1539-1540. |
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| 83. |
Szewczyk, J. W.; Zuckermann, R. L.; Bergman, R. G.; Ellman, J. A. A Mass Spectrometric Labeling Strategy for High-Throughput Reaction Evaluation and Optimization: Exploring C–H Activation Angew. Chem. Int. Ed. 2001, 40, 216-219. |
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| 82. |
Backes, B. J.; Harris, J. L.; Leonetti, F.; Ellman, J. A.; Craik, C. Rapid and General Profiling of Protease Specificity by Using Combinatorial Fluorogenic Substrate Libraries Proc. Natl. Acad. Sci. 2000, 97, 7754-7759. |
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| 81. |
Souers, A. J.; Rosenquist, A.; Jarvie, E. M.; Ladlow, M.; Fenuik, W.; Ellman, J. A. Optimization of a Somatostatin Mimetic via Constrained Amino Acid and Backbone Incorporation Bioorg. Med. Chem. Lett. 2000, 10, 2731-2733. |
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| 80. |
Lee, A.; Szewczyk, J. W.; Ellman, J. A. “Combinatorial Libraries for Drug Development” in Stimulating Concepts in Chemistry Vogtle, F.; Stoddart, J. F.; Shibasaki, M. Ed.; Wiley-VCH, Weinheim 2000, , 65-78. |
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| 79. |
Ellman, J. A. “Combinatorial Methods to Engineer Small Molecules for Functional Genomics” in Ernst Schering Research Foundation workshop Mulzer, J. and Bohlmann, R. Ed.; Springer 2000, , 183-204. |
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| 78. |
Bi, X.; Lin, B. Haque, T.; Lee, C. E.; Skillman, A. G.; Kuntz, I. D.; Ellman, J. A.; Lynch, G. Novel Cathepsin D Inhibitors Block the Formation of Hyperphosphorylated Tau Fragments in Hippocampus J. Neurochem. 2000, 74, 1469-1477. |
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| 77. |
Maly, D. J.; Choong, I. C.; Ellman, J. A. Combinatorial Target-Guided Ligand Assembly. Identification of Potent, Sub-type Selective c-Src Inhibitors Proc. Natl. Acad. Sci. 2000, 65, 1222-1224. |
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| 76. |
Souers, A. J.; Ellman, J. A. Asymmetric Synthesis of a C-3 Substituted Pipecolic Acid J. Org. Chem. 2000, 65, 1222-1224. |
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| 75. |
Backes, B. J.; Harris, J. L.; Leonetti, F.; Craik, C.; Ellman, J. A. Synthesis of positional-scanning libraries of fluorogenic peptide substrates to define the extended substrate specificity of plasmin and thrombin Nat. Biotechnol. 2000, 18, 187-194. |
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| 74. |
Shin, Y.; Winans, K. A.; Backes, B. J.; Kent, S. B. H.; Ellman, J. A.; Bertozzi, C. R. Fmoc-Based Synthesis of Peptide-Thioesters: Application to the Total Chemical Synthesis of a Glycoprotein by Native Chemical Ligation J. Am. Chem. Soc. 1999, 121, 11684-11689. |
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| 73. |
Lee, A.; Huang, L.; Ellman, J. A. General Solid-phase Method for the Preparation of Mechanism-Based Cysteine Protease Inhibitors J. Am. Chem. Soc. 1999, 121, 9907-9914. |
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| 72. |
Dragoli, D. R.; Ellman, J. A. Parallel Solid-Phase Synthesis of Prostaglandin E Analogs J. Comb. Chem. 1999, 1, 534-539. |
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| 71. |
Huang, L.; Lee, A.; Ellman, J. A. Targeted Libraries Proceedings of the 16th American Peptide Symposium 2000, , 161-163. |
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| 70. |
Haskell-Leuvano, C.; Souers, A. J.; Rosenquist, A., Ellman, J. A.; Cone, R. D. Identification of Agonists at the Human Melanocortin Receptor MC1R By the Evaluation of a Library of Small Molecules Based upon the b-Turn J. Med. Chem. 1999, 42, 4380-4387. |
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| 69. |
Ramdas, L.; Bunin, B. A.; Plunkett, M. J.; Sun, G.; Ellman, J. A.; Gallick, G.; Budde, R. J. A. Benzodiazepine Compounds as Inhibitors of the Src Protein Tyrosine Kinase: Screening of a Combinatorial Library of 1,4-Benzodiazepines Archives of Biochem. And Biophys. 1999, 368, 394-400. |
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| 68. |
Choong, I. C.; Ellman, J. A. Expedient Synthesis of Alkoxylamines Using tert-Butyl Oxaziridine: The First Direct Amination of Alcohols J. Org. Chem. 1999, 64, 6528-6529. |
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| 67. |
Borg, G.; Cogan, D. A.; Ellman, J. A. One-Pot Asymmetric Reductive Amination of Ketones to Prepare tert-Butanesulfinyl Protected Amines Tetrahedron Lett. 1999, 40, 6709-6712. |
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| 66. |
Backes, B. J.; Dragoli, D. R.; Ellman, J. A. Chiral N-Acyl-tert-Butanesulfinamides: The “Safety-Catch” Principle Applied to Diastereoselective Enolate Alkylations J. Org. Chem. 1999, 64, 5472-5478. |
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| 65. |
Xu, R.; Greiveldinger, G.; Marenus, L. E.; Cooper, A. G.; Ellman, J. A. Combinatorial Library Approach to the Development of Synthetic Receptors Targeting Vancomycin Resistant Bacteria J. Am. Chem. Soc. 1999, 55, 8883-8904. |
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| 64. |
Cogan, D. A.; Liu, G.; Ellman, J. A. Asymmetric Synthesis of Chiral Amines by Highly Diastereoselective 1,2-Additions of Organometallic Reagents to N-tert-Butanesulfinyl Imines Tetrahedron 1999, 55, 8883-8904. |
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| 63. |
Haque, T. S.; Skillman, A. G.; Lee, C. E.; Habashita, H.; Gluzman, I. Y.; Ewing, T. J. A.; Goldberg, D. E.; Kuntz, I. D.; Ellman, J. A. Single Digit Nanomolar, Low Molecular Weight Non-Peptide Inhibitors of Malarial Aspartyl Protease Plasmepsin II J. Med. Chem. 1999, 42, 1428-1440. |
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| 62. |
Backes, B. J.; Ellman, J. A. An Alkanesulfonamide “Safety-Catch” Linker for Solid-Phase Synthesis J. Org. Chem. 1999, 64, 2322-2330. |
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| 61. |
Souers, A. J.; Schürer, Kwack, H.; Virgilio, A. A.; Ellman, J. A. Preparation of Enantioenriched alpha-Bromo Acids with Diverse Side Chain Functionality Synthesis 1999, , 583-585. |
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| 60. |
Liu, G.; Cogan, D. A.; Owens, T. D.; Tang, T. P.; Ellman, J. A. The Synthesis of Enantiomerically Pure N-tert-Butanesulfinyl Imines (tert-Butanesulfinimines) by the Direct Condensation of tert-Butanesulfinamide with Aldehydes and Ketones J. Org. Chem. 1999, 64, 1278-1284. |
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| 59. |
Souers, A. J.; Virgilio, A. A.; Rosenquist, A.; Fenuik, W. Ellman, J. A. Identification of a Potent Heterocyclic Ligand to Somatostatin Receptor Sub-Type 5 by the Synthesis and Screening of beta-Turn Mimetic Libraries J. Am. Chem. Soc. 1999, 121, 1817-1825. |
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| 58. |
Cogan, D. A.; Ellman, J. A. The Asymmetric Synthesis of alpha,alpha-Dibranched Amines by the Trimethylaluminum Mediated 1,2-Addition of Organolithiums to tert-Butanesulfinyl Ketimines J. Am. Chem. Soc. 1999, 121, 268-269. |
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| 57. |
Tang, T. P.; Ellman, J. A. The tert-Butanesulfinyl Group: An Ideal Chiral Directing Group and Boc-Surrogate for Asymmetric beta-Amino Acid Synthesis and Applications J. Org. Chem. 1999, 64, 12-13. |
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| 56. |
Kim, K.; Volkman, S. K.; Ellman, J. A. Synthesis of 3-Substituted 1,4-Benzodiazepin-2-ones J. Braz. Chem. Soc. 1998, 9, 375-379. |
