Academic literature on the topic 'Trihydroxypiperidines'
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Journal articles on the topic "Trihydroxypiperidines"
Mirabella, S., G. Fibbi, C. Matassini, C. Faggi, A. Goti, and F. Cardona. "Accessing 2-substituted piperidine iminosugars by organometallic addition/intramolecular reductive amination: aldehyde vs. nitrone route." Organic & Biomolecular Chemistry 15, no. 43 (2017): 9121–26. http://dx.doi.org/10.1039/c7ob01848g.
Full textWood, Adam, Kate L. Prichard, Zane Clarke, Todd A. Houston, George W. J. Fleet, and Michela I. Simone. "Synthetic Pathways to 3,4,5-Trihydroxypiperidines from the Chiral Pool." European Journal of Organic Chemistry 2018, no. 48 (November 27, 2018): 6812–29. http://dx.doi.org/10.1002/ejoc.201800943.
Full textZhao, Hui, Wu-Bao Wang, Shinpei Nakagawa, Yue-Mei Jia, Xiang-Guo Hu, George W. J. Fleet, Francis X. Wilson, Robert J. Nash, Atsushi Kato, and Chu-Yi Yu. "Novel 2-aryl-3,4,5-trihydroxypiperidines: Synthesis and glycosidase inhibition." Chinese Chemical Letters 24, no. 12 (December 2013): 1059–63. http://dx.doi.org/10.1016/j.cclet.2013.06.027.
Full textPrichard, Kate, David Campkin, Nicholas O'Brien, Atsushi Kato, George W. J. Fleet, and Michela I. Simone. "Biological activities of 3,4,5-trihydroxypiperidines and their N - and O -derivatives." Chemical Biology & Drug Design 92, no. 1 (April 16, 2018): 1171–97. http://dx.doi.org/10.1111/cbdd.13182.
Full textYu, Chu-Yi, and et al et al. "ChemInform Abstract: Novel 2-Aryl-3,4,5-trihydroxypiperidines: Synthesis and Glycosidase Inhibition." ChemInform 45, no. 18 (April 17, 2014): no. http://dx.doi.org/10.1002/chin.201418214.
Full textClemente, F., C. Matassini, C. Faggi, S. Giachetti, C. Cresti, A. Morrone, P. Paoli, A. Goti, M. Martínez-Bailén, and F. Cardona. "Glucocerebrosidase (GCase) activity modulation by 2-alkyl trihydroxypiperidines: Inhibition and pharmacological chaperoning." Bioorganic Chemistry 98 (May 2020): 103740. http://dx.doi.org/10.1016/j.bioorg.2020.103740.
Full textClemente, Francesca, Camilla Matassini, Andrea Goti, Amelia Morrone, Paolo Paoli, and Francesca Cardona. "Stereoselective Synthesis of C-2 Alkylated Trihydroxypiperidines: Novel Pharmacological Chaperones for Gaucher Disease." ACS Medicinal Chemistry Letters 10, no. 4 (February 8, 2019): 621–26. http://dx.doi.org/10.1021/acsmedchemlett.8b00602.
Full textPrichard, Kate L., Nicholas O'Brien, Mahdi Ghorbani, Adam Wood, Evan Barnes, Atsushi Kato, Todd A. Houston, and Michela I. Simone. "Synthetic Routes to 3,4,5-Trihydroxypiperidines via Stereoselective and Biocatalysed Protocols, and Strategies toN- andO-Derivatisation." European Journal of Organic Chemistry 2018, no. 48 (November 27, 2018): 6830–42. http://dx.doi.org/10.1002/ejoc.201801011.
Full textSmith, Rachel D., and Neil R. Thomas. "A Convenient Synthesis of N-substituted Trihydroxypiperidines from Bis-Epoxides: Nucleophilic Opening of 1,2:4,5-Dianhydropentitols." Synlett 2000, no. 2 (February 2000): 193–96. http://dx.doi.org/10.1055/s-2000-6499.
Full textSmith, Rachel D., and Neil R. Thomas. "ChemInform Abstract: A Convenient Synthesis of N-Substituted Trihydroxypiperidines from Bis-epoxides: Nucleophilic Opening of 1,2:4,5-Dianhydropentitols." ChemInform 31, no. 21 (June 8, 2010): no. http://dx.doi.org/10.1002/chin.200021204.
Full textDissertations / Theses on the topic "Trihydroxypiperidines"
Brown, Peter John. "Synthetic studies towards inhibitors of mycobacterial galactose processing enzymes and trihydroxypiperidines." Thesis, University of Nottingham, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.273164.
Full textClemente, Francesca. "Synthesis of alkylated azasugars and their therapeutic potential against lysosomal storage and neurological disorders: the Gaucher-Parkinson case." Doctoral thesis, 2021. http://hdl.handle.net/2158/1234174.
Full textBook chapters on the topic "Trihydroxypiperidines"
Nag, Ahindra. "Diastereoselective Syntheses of 3,4,5-Trihydroxypiperidine Iminosugars." In Asymmetric Synthesis of Drugs and Natural Products, 163–76. Boca Raton : CRC Press, 2018.: CRC Press, 2018. http://dx.doi.org/10.9774/gleaf.9781315302317-5.
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