Clay S. Bennett, Ph.D.
Affiliations: | 2008- | Chemistry | Tufts University, Boston |
Website:
http://ase.tufts.edu/chemistry/bennett/clay-s-bennett.htmlGoogle:
"Clay Bennett"Mean distance: 7.32 | S | N | B | C | P |
Parents
Sign in to add mentor| Amos B. Smith, III | grad student | 1999-2005 | Penn | |
| (Synthetic studies on the spongistatin family of natural products: I. Development of a practical synthesis of the (16)-C(28) CD spiorketal. II. Computer aided design and synthetic progress towards spongistatin analogs with simplified molecular architectu) | ||||
| Chi-Huey Wong | post-doc | 2005-2008 | Scripps Institute | |
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Publications
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| Romeo JR, Lucera JD, Jensen D, et al. (2023) Application of Redox-Active Ester Catalysis to the Synthesis of Pyranose Alkyl -Glycosides. Organic Letters. 25: 3760-3765 |
| Galan MC, Kulkarni SS, Bennett CS. (2023) Editorial: Recent advances in carbohydrate chemical and enzymatic syntheses. Frontiers in Chemistry. 11: 1144042 |
| Mizia JC, Syed MU, Bennett CS. (2022) Synthesis of the α-Linked Digitoxose Trisaccharide Fragment of Kijanimicin: An Unexpected Application of Glycosyl Sulfonates. Organic Letters. 24: 731-735 |
| Bennett CS, Yalamanchili S, Nguyen TA, et al. (2021) Automated, Multistep Continuous-Flow Synthesis of 2,6-Dideoxy and 3-Amino-2,3,6-trideoxy Monosaccharide Building Blocks. Angewandte Chemie (International Ed. in English) |
| Yalamanchili S, Nguyen TV, Pohl NLB, et al. (2020) Modular continuous flow synthesis of orthogonally protected 6-deoxy glucose glycals. Organic & Biomolecular Chemistry |
| Romeo JR, McDermott L, Bennett CS. (2020) Reagent-Controlled α-Selective Dehydrative Glycosylation of 2,6-Dideoxy Sugars: Construction of the Arugomycin Tetrasaccharide. Organic Letters |
| Ling J, Bennett CS. (2019) Versatile Glycosyl Sulfonates in b-Selective C-Glycosylation. Angewandte Chemie (International Ed. in English) |
| Yalamanchili S, Miller W, Chen X, et al. (2019) Rapid Preparation of 2,6-Dideoxy Sugar Libraries through Gold-Catalyzed Homopropargyl Orthoester Cyclization. Organic Letters |
| Zhuo MH, Wilbur DJ, Kwan EE, et al. (2019) Matching Glycosyl Donor Reactivity to Sulfonate Leaving Group Ability Permits SN2 Glycosylations. Journal of the American Chemical Society |
| Ling J, Bennett CS. (2019) Recent Developments in Stereoselective Chemical Glycosylation. Asian Journal of Organic Chemistry. 8: 802-813 |