J. Prithika Yasomanee
Affiliations: | 2009-2014 | University of Missouri - Saint Louis |
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Sign in to add mentor| Alexei V. Demchenko | grad student | 2009-2014 | University of Missouri - Saint Louis |
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| Alex C, Visansirikul S, Zhang Y, et al. (2019) Synthesis of 2-azido-2-deoxy- and 2-acetamido-2-deoxy-D-manno derivatives as versatile building blocks. Carbohydrate Research. 488: 107900 |
| Mannino MP, Yasomanee JP, Demchenko AV. (2018) Investigation of the H-bond-mediated aglycone delivery reaction in application to the synthesis of β-glucosides. Carbohydrate Research. 470: 1-7 |
| Wang T, Nigudkar SS, Yasomanee JP, et al. (2018) Glycosyl nitrates in synthesis: streamlined access to glucopyranose building blocks differentiated at C-2. Organic & Biomolecular Chemistry |
| Bandara MD, Yasomanee JP, Rath NP, et al. (2016) Conformationally superarmed S-ethyl glycosyl donors as effective building blocks for chemoselective oligosaccharide synthesis in one pot. Organic & Biomolecular Chemistry |
| Nigudkar SS, Wang T, Pistorio SG, et al. (2016) OFox imidates as versatile glycosyl donors for chemical glycosylation. Organic & Biomolecular Chemistry |
| Yasomanee JP, Visansirikul S, Pornsuriyasak P, et al. (2016) The synthesis of the repeating unit of capsular polysaccharide Staphylococcus aureus type 5 to study chemical activation and conjugation of native CP5. The Journal of Organic Chemistry |
| Yasomanee JP, Parameswar AR, Pornsuriyasak P, et al. (2016) 2,3-Di-O-picolinyl building blocks as glycosyl donors with switchable stereoselectivity. Organic & Biomolecular Chemistry. 14: 3159-69 |
| Kayastha AK, Jia XG, Yasomanee JP, et al. (2015) 6-O-Picolinyl and 6-O-Picoloyl Building Blocks As Glycosyl Donors with Switchable Stereoselectivity. Organic Letters. 17: 4448-51 |
| Visansirikul S, Yasomanee JP, Pornsuriyasak P, et al. (2015) A Concise Synthesis of the Repeating Unit of Capsular Polysaccharide Staphylococcus aureus Type 8. Organic Letters. 17: 2382-4 |
| Yasomanee JP, Demchenko AV. (2015) Hydrogen-bond-mediated aglycone delivery (HAD): a highly stereoselective synthesis of 1,2-cis α-D-glucosides from common glycosyl donors in the presence of bromine. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 6572-81 |