200. |
Brak, K.; Ellman, J. A.
Asymmetric Synthesis of α–Branched Allylic Amines by the Rh(I)-Catalyzed Addition of Alkenyltrifluoroborates to N-tert-Butanesulfinyl Aldimines
J. Am. Chem. Soc. 2009, 131, 3850–3851.
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199. |
Yotphan, S.; Bergman, R. G.; Ellman, J. A.
Application of Daugulis Copper-Catalyzed Direct Arylation to the Synthesis of 5-Aryl Benzotriazepines
Org. Lett. 2009, 11, 1511–1514.
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198. |
Wakayama , M.; Ellman, J. A.
Recycling the tert-Butanesulfinyl Group in the Synthesis of Amines Using tert-ButanesulfinamideRecycling the tert-Butanesulfinyl Group in the Synthesis of Amines Using tert-Butanesulfinamide
J. Org. Chem. 2009, 74, 2646–2650. Write-up in Organic Process Research and Development
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197. |
Berman, A. M.; Lewis, J. C.; Bergman, R. G.; Ellman, J. A.
Rh(I)-Catalyzed Direct Arylation of Pyridines and Quinolines
J. Am. Chem. Soc. 2008, 130, 14926–14927.
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196. |
Harada, H.; Thalji, R. K.; Bergman, R. G.; Ellman, J. A.
Enantioselective Intramolecular Hydroarylation of Alkenes via Directed C-H Bond Activation
J. Org. Chem. 2008, 73, 6772-6779.
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195. |
Lewis, J. C.; Bergman, R. G.; Ellman, J. A.
Direct Functionalization of Nitrogen Heterocycles via Rh-Catalyzed C-H Bond Activation
Acc. Chem. Res. 2008, 41, 1013-1025.
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194. |
Drag, M.; Mikolajczyk, J.; Bekes, M.; Reyes-Turcu, F.; Ellman, J. A.; Wilkinson, K. D.; Salvesen, G. S.
Positional-Scanning Fluorogenic Substrate Libraries Reveal Unexpected Specificity Determinants of Deubiquitinating Enzymes (DUBs)
Biochem. J. 2008, 415, 367-375.
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193. |
Trincado, M.; Ellman, J. A.
Enantioselective Synthesis of alpha-Aryl Alkylamines by Rh-Catalyzed Addition Reactions of Arylboronic Acids to Aliphatic Imines
Angew. Chem. Int. Ed. 2008, 47, 5623-5626.
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192. |
Beenen, M. A.; An, C.; Ellman, J. A.
Asymmetric Copper-Catalyzed Synthesis of alpha-Amino Boronate Esters from N-tert-Butanesulfinyl Aldimines
J. Am. Chem. Soc. 2008, 130, 6910-6911.
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191. |
Patterson, A. W.; Peltier, H. M.; Ellman, J. A.
Expedient Synthesis of N-Methyl Tubulysin Analogues with High Cytotoxicity
J. Org. Chem. 2008, 73, 4362-4369.
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190. |
Gribble, M. W.; Ellman, J. A.; Bergman, R. G.
Synthesis of a Benzodiazepine-Derived Rhodium NHC Complex by C-H Bond Activation
Organometallics 2008, 27, 2152-2155.
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189. |
Brak, K.; Doyle, P. S.; McKerrow, J. H.; Ellman, J. A.
Identification of a New Class of Nonpeptidic Inhibitors of Cruzain
J. Am. Chem. Soc. 2008, 130, 6404-6410.
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188. |
Tsai, A. S.; Bergman, R. G.; Ellman, J. A.
Asymmetric Synthesis of (−)-Incarvillateine Employing an Intramolecular Alkylation via Rh-Catalyzed Olefinic C−H Bond Activation
J. Am. Chem. Soc. 2008, 130, 6316-6317.
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187. |
Colby, D. A.; Bergman, R. G.; Ellman, J. A.
Synthesis of Dihydropyridines and Pyridines from Imines and Alkynes via C-H Activation
J. Am. Chem. Soc. 2008, 130, 3645-3651.
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186. |
Yotphan, S.; Bergman, R. G.; Ellman, J. A.
The Stereoselective Formation of Bicyclic Enamines with Bridgehead Unsaturation via Tandem C-H Bond Activation/Alkenylation/Electrocyclization
J. Am. Chem. Soc. 2008, 130, 2452-2453.
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185. |
Lewis, J. C.; Berman, A. M.; Bergman, R. G.; Ellman, J. A.
Rh(I)-Catalyzed Arylation of Heterocycles via C-H Bond Activation: Expanded Scope Through Mechanistic Insight.
J. Am. Chem. Soc. 2008, 130, 2493-2500.
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184. |
Robak, M. T.; Trincado, M.; Ellman, J. A.
Enantioselective Aza-Henry Reaction with an N-Sulfinyl Urea Organocatalyst
J. Am. Chem. Soc. 2007, 129, 15110-15111.
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183. |
Nakagawa, H.; Rech, J. C.; Sindelar, R. W.; Ellman, J. A.
Catalytic Enantioselective Addition of Arylboronic Acids to N-Boc Imines Generated in Situ
Org. Lett. 2007, 9, 5155-5157. Write-up in Organic Process Research and Development
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182. |
Patterson, A. W.; Peltier, H. M.; Sasse, F.; Ellman, J. A.
Design, Synthesis, and Biological Properties of Highly Potent Tubulysin D Analogues
Chem. Eur. J. 2007, 13, 9534-9541.
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181. |
Tanuwidjaja, J.; Peltier, H. M.; Lewis, J. C.; Schenkel, L. B.; Ellman, J. A.
One-Pot Microwave-Promoted Synthesis of Nitriles from Aldehydes via tert-Butanesulfinyl Imines
Synthesis 2007, , 3385-3389.
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180. |
Watzke, A.; Wilson, R. M.; O’Malley, S. J.; Bergman, R. G.; Ellman, J. A.
Asymmetric Intramolecular Alkylation of Chiral Aromatic Imines via Catalytic C-H Bond Activation
Synlett 2007, , 2383-2389.
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179. |
Soellner, M. B.; Rawles, K. A.; Grundner, C.; Alber, T.; Ellman, J. A.
Fragment-Based Substrate Activity Screening Method for the Identification of Potent Inhibitors of the M. tuberculosis Phosphatase PtpB
J. Am. Chem. Soc. 2007, 129, 9613-9615. Research Highlight in Nature Chemical Biology
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178. |
Rosa-Bauza, Y. T.; Berst, F.; Ellman, J. A.
Straightforward Preparation and Assay of Aspartyl Protease Substrates with an Internal Thioester Linkage
ChemBioChem 2007, 8, 981-984.
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177. |
Ellman, J. A
The Direct Approach
Science 2007, 316, 1131-1132.
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176. |
Inagaki, H.; Tsuruoka, H.; Hornsby, M.; Lesley, S. A.; Spraggon, G.; Ellman, J. A.
Nonpeptidic Inhibitors of Cathepsin S with an Unprecedented Binding Mode
J. Med. Chem. 2007, 50, 2693-2699.
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175. |
Lewis, J. C.; Bergman, R. G.; Ellman, J. A.
Rh(I)-Catalyzed Alkylation of Quinolines and Pyridines via C-H Bond Activation
J. Am. Chem. Soc. 2007, 129, 5332-5333. Write-up in Organic Process Research and Development
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174. |
Rech, J. C.; Yato, M.; Duckett, D.; Ember, Brian; LoGrasso, P. V.; Bergman, R. G.; Ellman, J. A.
Synthesis of Potent Bicyclic Bisarylimidazole c-Jun N-Terminal Kinase Inhibitors by Catalytic C-H Bond Activation
J. Am. Chem. Soc. 2007, 129, 490-491.
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173. |
Tanuwidjaja, J.; Peltier, H. M.; Ellman, J. A
One-Pot Asymmetric Synthesis of Either Diastereomer of tert-Butanesulfinyl-protected Amines from Ketones
J. Org. Chem. 2007, 72, 626-629.
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172. |
Liu, G. L.; Rosa-Bauza, Y. T.; Salisbury, C. T.; Lu, Y.; Kim, J.; Craik, C.; Ellman, J. A.; Lee, L. P.; Chen, F. F.
Peptide-Nanocrescent Hybrid SERS Probe for Optical Detection of Protease Activity
J. Nanoscience Nanotech. 2007, 7, 2323–2330.
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171. |
Peltier, H. M.; McMahon, J. P.; Patterson, A. W.; Ellman, J. A.
The Total Synthesis of Tubulysin D
J. Am. Chem. Soc. 2006, 128, 16018-16019.
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