Philip C. Hogan, Ph.D.
Affiliations: | 2004 | Harvard University, Cambridge, MA, United States |
Area:
synthesis of natural productsGoogle:
"Philip Hogan"Mean distance: 8.28 | S | N | B | C | P |
Parents
Sign in to add mentor| Andrew G. Myers | grad student | 2004 | Harvard | |
| (Enantioselective synthesis of kedarcidin chromophore aglycon.) | ||||
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Publications
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| Hogan PC, Chen CL, Mulvihill KM, et al. (2017) Large-scale preparation of key building blocks for the manufacture of fully synthetic macrolide antibiotics. The Journal of Antibiotics |
| Ren F, Hogan PC, Anderson AJ, et al. (2007) Synthesis of L-kedarosamine in protected form and its efficient incorporation into an advanced intermediate to kedarcidin chromophore. Organic Letters. 9: 1923-5 |
| Ren F, Hogan PC, Anderson AJ, et al. (2007) Kedarcidin chromophore: synthesis of its proposed structure and evidence for a stereochemical revision. Journal of the American Chemical Society. 129: 5381-3 |
| Hogan PC, Corey EJ. (2005) Proteasome inhibition by a totally synthetic beta-lactam related to salinosporamide A and omuralide. Journal of the American Chemical Society. 127: 15386-7 |
| Myers AG, Hogan PC, Hurd AR, et al. (2002) Enantioselective synthesis of kedarcidin chromophore aglycon in differentially protected form. Angewandte Chemie (International Ed. in English). 41: 1062-7 |
| Myers AG, Hurd AR, Hogan PC. (2002) Evidence for facile atropisomerism and simple (non-nucleophilic) biradical-forming cycloaromatization within kedarcidin chromophore aglycon. Journal of the American Chemical Society. 124: 4583-5 |