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  1. 1.   O-Glycosidation reactions promoted by in situ generated silver N-heterocyclic carbenes in ionic liquids
  2. Talisman, I. J.; Kumar, V.; Razzaghy, J.; Malhotra, S. V.
  3. Carbohydrate Research. 2011, May; 346(7): 883-890.
  1. 2.   Application of ring-closing metathesis macrocyclization to the development of Tsg101-binding antagonists
  2. Liu, F.; Stephen, A. G.; Waheed, A. A.; Freed, E. O.; Fisher, R. J.; Burke, T. R.
  3. Bioorganic & Medicinal Chemistry Letters. 2010, Jan; 20(1): 318-321.
  1. 3.   Identification of Shc Src Homology 2 Domain-Binding Peptoid-Peptide Hybrids
  2. Choi, W. J.; Kim, S. E.; Stephen, A. G.; Weidlich, I.; Giubellino, A.; Liu, F.; Worthy, K. M.; Bindu, L.; Fivash, M. J.; Nicklaus, M. C.; Bottaro, D. P.; Fisher, R. J.; Burke, T. R.
  3. Journal of Medicinal Chemistry. 2009 52(6): 1612-1618.
  1. 4.   Synthesis of a homologous series of side-chain-extended orthogonally protected aminooxy-containing amino acids
  2. Liu, F.; Thomas, J.; Burke, T. R.
  3. Synthesis-Stuttgart. 2008 (15): 2432-2438.
  1. 5.   Design and synthesis of redox stable analogues of sunflower trypsin inhibitors (SFTI-1) on solid support, potent inhibitors of matriptase
  2. Jiang, S.; Li, P.; Lee, S. L.; Lin, C. Y.; Long, Y. Q.; Johnson, M. D.; Dickson, R. B.; Roller, P. P.
  3. Organic Letters. 2007, Jan; 9(1): 9-12.
  1. 6.   Utilization of achiral alkenyl amines for the preparation of high affinity Grb2 SH2 domain-binding macrocycles by ring-closing metathesis
  2. Liu, F.; Worthy, K. M.; Bindu, L.; Giubellino, A.; Bottaro, D. P.; Fisher, R. J.; Burke, T. R.
  3. Organic & Biomolecular Chemistry. 2007 5(2): 367-372.
  1. 7.   Application of azide-alkyne cycloaddition 'click chemistry' for the synthesis of Grb2 SH2 domain-binding macrocycles
  2. Choi, W. J.; Shi, Z. D.; Worthy, K. M.; Bindu, L.; Karki, R. G.; Nicklaus, M. C.; Fisher, R. J.; Burke, T. R.
  3. Bioorganic & Medicinal Chemistry Letters. 2006, Oct; 16(20): 5265-5269.
  1. 8.   Development of Grb2 SH2 domain signaling antagonists: A potential new class of antiproliferative agents
  2. Burke, T. R.
  3. International Journal of Peptide Research and Therapeutics. 2006, Mar; 12(1): 33-48.
  1. 9.   Synthesis of bicyclo 3.1.0 hexanes functionalized at the tip of the cyclopropane ring. Application to the synthesis of carbocyclic nucleosides
  2. Comin, M. J.; Parrish, D. A.; Deschamps, J. R.; Marquez, V. E.
  3. Organic Letters. 2006, Feb; 8(4): 705-708.
  1. 10.   Synthesis of a C-terminally biotinylated macrocyclic peptide mimetic exhibiting high Grb2 SH2 domain-binding affinity
  2. Shi, Z. D.; Liu, H. P.; Zhang, M. C.; Worthy, K. M.; Bindu, L.; Yang, D. J.; Fisher, R. J.; Burke, T. R.
  3. Bioorganic & Medicinal Chemistry. 2005, JUL 1; 13(13): 4200-4208.
  1. 11.   Examination of phosphoryl-mimicking functionalities within a macrocyclic Grb2 SH2 domain-binding platform
  2. Kang, S. U.; Shi, Z. D.; Worthy, K. M.; Bindu, L. K.; Dharmawardana, P. G.; Choyke, S. J.; Bottaro, D. P.; Fisher, R. J.; Burke, T. R.
  3. Journal of Medicinal Chemistry. 2005, JUN 16; 48(12): 3945-3948.
  1. 12.   Ring-closing metathesis of C-terminal allylglycine residues with an N-terminal beta-vinyl-substituted phosphotyrosyl mimetic as an approach to novel Grb2 SH2 domain-binding macrocycles
  2. Oishi, S.; Shi, Z. D.; Worthy, K. M.; Bindu, L. K.; Fisher, R. J.; Burke, T. R.
  3. Chembiochem. 2005, APR; 6(4): 668-674.
  1. 13.   Evaluation of macrocyclic Grb2 SH2 domain-binding peptide mimetics prepared by ring-closing metathesis of C-terminal allylglycines with an N-terminal beta-vinyl-substituted phosphotyrosyl mimetic
  2. Oishi, S.; Karki, R. G.; Shi, Z. D.; Worthy, K. M.; Bindu, L.; Chertov, O.; Esposito, D.; Frank, P.; Gillette, W. K.; Maderia, M.; Hartley, J.; Nicklaus, M. C.; Barchi, J. J.; Fisher, R. J.; Burke, T. R.
  3. Bioorganic & Medicinal Chemistry. 2005 13(7): 2431-2438.
  1. 14.   Synthesis of a 5-methylindolyl-containing macrocycle that displays ultrapotent Grb2 SH2 domain-binding affinity
  2. Shi, Z. D.; Lee, K.; Wei, C. Q.; Roberts, L. R.; Worthy, K. M.; Fisher, R. J.; Burke, T. R.
  3. Journal of Medicinal Chemistry. 2004 47(4): 788-791.
  1. 15.   Enantioselective synthesis of metathesis-derived ureapeptoid macrocycles
  2. Wang, X. Z.; Burke, T. R.
  3. Synlett. 2004 (3): 469-472.
  1. 16.   Macrocyclization in the design of Grb2 SH2 domain-binding ligands exhibiting high potency in whole-cell systems
  2. Wei, C. Q.; Gao, Y.; Lee, K.; Guo, R.; Li, B. H.; Zhang, M. C.; Yang, D. J.; Burke, T. R.
  3. Journal of Medicinal Chemistry. 2003 46(2): 244-254.
  1. 17.   Current synthetic approaches to peptide and peptidomimetic cyclization
  2. Li, P.; Roller, P. P.; Xu, J. C.
  3. Current Organic Chemistry. 2002 6(5): 411-440.
  1. 18.   Olefin metathesis in the design and synthesis of a globally constrained Grb2 SH2 domain inhibitor
  2. Gao, Y.; Wei, C. Q.; Burke, T. R.
  3. Organic Letters. 2001 3(11): 1617-1620.
  1. 19.   Designed Epothilones - Combinatorial Synthesis, Tubulin Assembly Properties, and Cytotoxic Action Against Taxol-Resistant Tumor Cells
  2. Nicolaou, K. C.; Vourloumis, D.; Li, T. H.; Pastor, J.; Winssinger, N.; He, Y.; Ninkovic, S.; Sarabia, F.; Vallberg, H.; Roschangar, F.; King, N. P.; Finlay, M. R. V.; Giannakakou, P.; Verdierpinard, P.; Hamel, E.
  3. Angewandte Chemie-International Edition. 1997 36(19): 2097-2103.
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