Contact Information
Office: WEL: 4.320
Phone: 471-3966
Lab
Office:
Phone:
Fax: 471-7839
Philip D. Magnus
p.magnus@mail.utexas.edu
Professor, Faculty
R.P. Doherty Jr. - Welch Regents Chair
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Research Group
Magnus Group |
Education
BSc, ., 1965 PhD, Imperial College, 1968 DSc, London University, 1982
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Awards
Novartis Research Award, 1998 Robert Robinson Award of the Royal Society of Chemistry, 1996 Fellow of the Royal Society of London, 1985
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Synthesis of biologically important natural products and the development of new reactions
Currently, we are working on the synthesis of the antitumor marine alkaloid diazonamide using a newly discovered phenolic ether rearrangement. The synthesis of a class of antitumor antibiotics called the rocaglates is near completion. The strategy is completely regio- and stereoselective. The alkaloid synthesis program includes saframycin, lemonomycin, galanthamine, salutaridine, daphnicyclidine A, chartelline C, cephalocyclidine and nakadomarin. All of the projects involve the development of new concise strategies, and this in course, frequently leads to the discovery of new reactions.
Representative Publications
P. Magnus and R.Turnbull "Thermal and Acid Catalyzed Hofmann-Martius Rearrangement of 3-N-Aryl-2-Oxindoles into 3-(Arylamino)-2-Oxindoles." Organic Letters 8 (2006): 3497-3499.
P. Magnus and A. Padilla "Proposed Biogenetic Origin of Secu'amamine A from Allosecurinine: A Model Study to Support the Intermediacy of the Putative Aziridinium Ion." Organic Letters 8 (2006): 3569-3571.
F. W. Goldberg, P. Magnus and R.Turnbull "A Mild Thermal and Acid Catalyzed Rearrangement of O-Aryl Ethers into Ortho-Hydroxy Arenes." Organic Letters 7 (2005): 4531-4534.
P. Magnus and K. S. Matthews "Stereoselective Synthesis of the Tetrahydroisoquinoline Alkaloid (+/-)-Renieramycin G and a (+/-)-Lemonomycinone Analogue from a Common Intermediate." J. Am. Chem. Soc. 127 (2005): 12476-12477.
P. Magnus, and M. A. H. Stent "Stereospecific Synthesis of (+/-)-1,2-Anhydro Methyl Rocaglate." Organic Letters 7 (2005): 3853-3855.