Angie R. Angeles, Ph.D.
Affiliations: | 2005 | University of Pennsylvania, Philadelphia, PA, United States |
Area:
Natural product synthesisGoogle:
"Angie Angeles"Mean distance: 7.45
Parents
Sign in to add mentor| Amos B. Smith, III | grad student | 2005 | Penn | |
| (The design and synthesis of novel ligands for the somatostatin and NK1 receptors incorporating the beta-D-glucoside scaffold and related mimetics of peptidal beta-turns.) | ||||
| Samuel J. Danishefsky | post-doc | Columbia | ||
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Publications
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| Peng F, Dai M, Angeles AR, et al. (2012) Permuting Diels-Alder and Robinson Annulation Stereopatterns. Chemical Science (Royal Society of Chemistry : 2010). 3: 3076-3080 |
| Kim WH, Angeles AR, Lee JH, et al. (2009) Concise Synthesis of the Xenibellols Core. Tetrahedron Letters. 50: 6440-6441 |
| Hirschmann RF, Nicolaou KC, Angeles AR, et al. (2009) The beta-D-glucose scaffold as a beta-turn mimetic. Accounts of Chemical Research. 42: 1511-20 |
| Angeles AR, Waters SP, Danishefsky SJ. (2008) Total syntheses of (+)- and (-)-peribysin E. Journal of the American Chemical Society. 130: 13765-70 |
| Angeles AR, Dorn DC, Kou CA, et al. (2007) Total synthesis of peribysin E necessitates revision of the assignment of its absolute configuration. Angewandte Chemie (International Ed. in English). 46: 1451-4 |
| Danishefsky S, Angeles A, Dorn D, et al. (2007) Synthesis of ent-Peribysin E Synfacts. 2007: 0678-0678 |
| Mowery BP, Prasad V, Kenesky CS, et al. (2006) Catechol: A minimal scaffold for non-peptide peptidomimetics of the i + 1 and i + 2 positions of the beta-turn of somatostatin. Organic Letters. 8: 4397-400 |
| Angeles AR, Neagu I, Birzin ET, et al. (2005) Synthesis and binding affinities of novel SRIF-mimicking beta-D-glucosides satisfying the requirement for a pi-cloud at C1. Organic Letters. 7: 1121-4 |
| Kaul R, Angeles AR, Jäger M, et al. (2001) Incorporating beta-turns and a turn mimetic out of context in loop 1 of the WW domain affords cooperatively folded beta-sheets. Journal of the American Chemical Society. 123: 5206-12 |