Hillary M. Peltier, Ph.D. - Publications
Affiliations: | 2007 | University of California, Berkeley, Berkeley, CA, United States |
Area:
chemical synthesisYear | Citation | Score | |||
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2013 | Cusack KP, Koolman HF, Lange UEW, Peltier HM, Piel I, Vasudevan A. Emerging technologies for metabolite generation and structural diversification Bioorganic and Medicinal Chemistry Letters. 23: 5471-5483. PMID 23992859 DOI: 10.1016/J.Bmcl.2013.08.003 | 0.356 | |||
2008 | Patterson AW, Peltier HM, Ellman JA. Expedient synthesis of N-methyl tubulysin analogues with high cytotoxicity. The Journal of Organic Chemistry. 73: 4362-9. PMID 18479168 DOI: 10.1021/Jo800384X | 0.684 | |||
2007 | Patterson AW, Peltier HM, Sasse F, Ellman JA. Design, synthesis, and biological properties of highly potent tubulysin D analogues. Chemistry (Weinheim An Der Bergstrasse, Germany). 13: 9534-41. PMID 17828721 DOI: 10.1002/Chem.200701057 | 0.677 | |||
2007 | Tanuwidjaja J, Peltier HM, Ellman JA. One-pot asymmetric synthesis of either diastereomer of tert-butanesulfinyl-protected amines from ketones. The Journal of Organic Chemistry. 72: 626-9. PMID 17221983 DOI: 10.1021/Jo0616512 | 0.676 | |||
2007 | Tanuwidjaja J, Peltier HM, Lewis JC, Schenkel LB, Ellman JA. One-pot microwave-promoted synthesis of nitriles from aldehydes via tert-butanesulfinyl imines Synthesis. 3385-3389. DOI: 10.1055/S-2007-990805 | 0.669 | |||
2007 | Peltier HM, McMahon JP, Patterson AW, Ellman JA. The Total Synthesis of Tubulysin D (I). Cheminform. 38. DOI: 10.1002/chin.200719171 | 0.68 | |||
2006 | Peltier HM, McMahon JP, Patterson AW, Ellman JA. The total synthesis of tubulysin D. Journal of the American Chemical Society. 128: 16018-9. PMID 17165738 DOI: 10.1021/Ja067177Z | 0.678 | |||
2005 | Peltier HM, Ellman JA. N-sulfinyl metalloenamine conjugate additions: asymmetric synthesis of piperidines. The Journal of Organic Chemistry. 70: 7342-5. PMID 16122257 DOI: 10.1021/Jo051020S | 0.633 | |||
2005 | Peltier HM, Evans JW, Ellman JA. Catalytic enantioselective sulfinyl transfer using cinchona alkaloid catalysts. Organic Letters. 7: 1733-6. PMID 15844893 DOI: 10.1021/Ol050275P | 0.632 | |||
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