Year |
Citation |
Score |
2017 |
Hughes D, Wheeler P, Ene D. Olefin Metathesis in Drug Discovery and Development—Examples from Recent Patent Literature Organic Process Research & Development. 21: 1938-1962. DOI: 10.1021/Acs.Oprd.7B00319 |
0.38 |
|
2016 |
Wheeler P, Phillips JH, Pederson RL. Scalable Methods for the Removal of Ruthenium Impurities from Metathesis Reaction Mixtures Organic Process Research and Development. 20: 1182-1190. DOI: 10.1021/Acs.Oprd.6B00138 |
0.321 |
|
2014 |
Hsieh SY, Wanner B, Wheeler P, Beauchemin AM, Rovis T, Bode JW. Stereoelectronic basis for the kinetic resolution of N-heterocycles with chiral acylating reagents. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 7228-31. PMID 24839065 DOI: 10.1002/Chem.201402818 |
0.489 |
|
2013 |
Wheeler P, Vora HU, Rovis T. Asymmetric NHC-catalyzed synthesis of α-fluoroamides from readily accessible α-fluoroenals. Chemical Science (Royal Society of Chemistry : 2010). 4: 1674-1679. PMID 25346841 DOI: 10.1039/C3Sc00089C |
0.516 |
|
2012 |
Vora HU, Wheeler P, Rovis T. Exploiting Acyl and Enol Azolium Intermediates via NHeterocyclic Carbene Catalyzed Reactions of Alpha-Reducible Aldehydes. Advanced Synthesis & Catalysis. 354: 1617-1639. PMID 23538785 DOI: 10.1002/Adsc.201200031 |
0.543 |
|
2009 |
Achmatowicz M, Thiel OR, Wheeler P, Bernard C, Huang J, Larsen RD, Faul MM. Practical synthesis of a p38 MAP kinase inhibitor. The Journal of Organic Chemistry. 74: 795-809. PMID 19086898 DOI: 10.1021/Jo802186M |
0.317 |
|
2009 |
Thiel OR, Achmatowicz M, Bernard C, Wheeler P, Savarin C, Correll TL, Kasparian A, Allgeier A, Bartberger MD, Tan H, Larsen RD. Development of a practical synthesis of a p38 MAP kinase inhibitor Organic Process Research and Development. 13: 230-241. DOI: 10.1021/Op800250V |
0.377 |
|
2007 |
Achmatowicz M, Chan J, Wheeler P, Liu L, Faul MM. Comparative approaches toward diamines containing spatially separated homobenzylic and benzylic nitrogen stereocenters Tetrahedron Letters. 48: 4825-4829. DOI: 10.1016/J.Tetlet.2007.05.073 |
0.356 |
|
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