Snowden-2013
  • 2046 Shelby Hall
  • (205) 348-8550
  • (205) 348-9104
Timothy S. Snowden
Associate Professor
2046 Shelby Hall
Education: Undergraduate Degree

B.S., 1994, Clemson University

Education: Doctoral Degree

Ph.D., 2001, The University of Texas at Austin

Education: Other

NIH Post-doctoral Fellow, 2001-2003, University of Pennsylvania

Research Interests

Synthetic Methodology; Natural Product Synthesis

Methods Development

One area of our research program features the development of sequential, ìone-potî, carbon-carbon bond-forming reactions to generate structures that are difficult to obtain by currently available synthetic routes. One such method involves the preparation of polysubstituted aromatic compounds via the strategic, regioselective, difunctionalization of arynes. This approach is designed to offer a concise preparation of the aromatic segments of several medicinally intriguing natural products.

C-Glycosides act as inhibitors of carbohydrate processing enzymes (e.g., glycosidases) involved in such diseases as HIV, diabetes, and cancer. C-Glycosides are also non-hydrolysable analogs of glycans vital to intra-, and intercellular signal processing and metabolism and are structural components of, or building blocks for, a number of interesting natural products (e.g., spongistatin, halichondrin B, brevetoxins, palytoxin). We are exploring a rapid and versatile approach to C-glycopyranosides and associated analogs. This method is expected to provide convenient access to readily modifiable precursors of, for example, 2- or 3-deoxy-, fluoro-, and amino-C-glycosides. Variations of this procedure are also expected to lead to stereoselective preparations of mono- and disubstituted cycloalkanones, polycyclic ethers, lactones, lactams, pyranones, and aminoimidazolones. The mechanisms by which this multi-step, ìone-potî process proceeds are also curiosities and will be investigated by physical organic methods.

Total Synthesis of Xenicanes

Xenicanes are a large, diverse class of diterpenes and norditerpenes isolated from marine organisms. Many of these compounds exhibit potent cytotoxic, anti-angiogenic, antifungal, or anti-inflammatory activities. Xenicanes possess the general skeletal structure depicted below which bears a cyclononene ring typically attached to a polysubstituted lactone, glycal, or cyclobutane. We are examining new routes to the total synthesis of these biologically and structurally interesting natural products using sequential reactions to construct several key portions of the targets.

Representative Publications

Snider, J.; Entrekin, J. T.; Snowden, T. S.; Dolliver, D. Synthesis of Potent CERT Inhibitor HPA-12 Featuring a Tandem Corey-Link and Intramolecular Nucleophilic Acyl Substitution Reaction.Synthesis 201345, 1899-1903.

Ganta, A.; Shamshina, J. L; Cafiero, L. R.; Snowden, T. S. Stereoselective Synthesis of cis- or trans-2,4-Disubstituted Butyrolactones from Wynberg Lactone. Tetrahedron 201268, 5396-5405.

Gupta, M. K.; Li, Z.; Snowden, T. S. One-Pot Synthesis of Trichloromethyl Carbinols from Primary Alcohols. J. Org. Chem. 201277, 4854-4860.

Snowden, T.S. Recent Synthetic Applications Involving gem-Dichloroepoxides. ARKIVOC, 2012, ii, 24-40.

Ganta, A.; Snowden, T. S.  Carbocupration-Functionalization of Arynes – Rapid Access to Variably ortho-Substituted ((E)-3-Phenylprop-1-enyl)silanes. Org. Lett. 200810, 5103-5106.

Cafiero, L. R.; Snowden, T. S.  General and Practical Conversion of Aldehydes to Homologated Carboxylic Acids. Org. Lett. 200810, 3853-3856.

Carr, J. A.; Snowden, T.S.  Comparative Reductive Desymmetrization of Cyclic 2,2-Disubstituted-1,3-Diones, Tetrahedron 200864, 2897-2905.

Ganta, A.; Snowden, T. S.  Facile Preparation of 2-Iodoaryl Trifluoromethanesulfonates – Superior Aryne Precursors.  Synlett 200714, 2227-2231.

Shamshina, J. L.; Snowden, T. S. Convergent synthesis of potent COX-2 inhibitor inotilone, Tetrahedron Lett. 200748, 3767-3769.

Shamshina, J. L.; Snowden, T. S.  Practical Approach to a- or g-Heterosubstituted Enoic Acids.  Org. Lett. 20068, 5881-5884.