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  1. 1.   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. 2.   Utilization of a common pathway for the synthesis of high affinity macrocyclic Grh2 SH2 domain-binding peptide mimetics that differ in the configuration at one ring junction
  2. Shi, Z. D.; Karki, R. G.; Worthy, K. M.; Bindu, L. K.; Nicklaus, M. C.; Fisher, R. J.; Burke, T. R.
  3. Chemistry & Biodiversity. 2005 2(4): 447-456.
  1. 3.   Examination of the role of phosphoryl-mimicking functionality in the binding of picomolar-affinity Grb2 SH2 domain-binding macrocycles
  2. Kang, S.; Shi, Z. D.; Lee, K.; Worthy, K. M.; Fisher, R. J.; Burke, T. R.
  3. Abstracts of Papers of the American Chemical Society. 2004, MAR 28; 227(041-MEDI, Part 2): U12-U12.
  1. 4.   Enantioselective synthesis of metathesis-derived ureapeptoid macrocycles
  2. Wang, X. Z.; Burke, T. R.
  3. Synlett. 2004 (3): 469-472.
  1. 5.   Synthesis and biological activity of a novel C4-C6 bridged paclitaxel analog
  2. Yuan, H. Q.; Kingston, D. G. I.; Sackett, D. L.; Hamel, E.
  3. Tetrahedron. 1999 55(32): 9707-9716.
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