A selective and mild glycosylation method of natural phenolic alcohols

Mária Mastihubová and Monika Poláková
Beilstein J. Org. Chem. 2016, 12, 524–530. https://doi.org/10.3762/bjoc.12.51

Supporting Information

Supporting Information File 1: Experimental procedures and analytical data.
Format: PDF Size: 265.2 KB Download

Cite the Following Article

A selective and mild glycosylation method of natural phenolic alcohols
Mária Mastihubová and Monika Poláková
Beilstein J. Org. Chem. 2016, 12, 524–530. https://doi.org/10.3762/bjoc.12.51

How to Cite

Mastihubová, M.; Poláková, M. Beilstein J. Org. Chem. 2016, 12, 524–530. doi:10.3762/bjoc.12.51

Download Citation

Citation data can be downloaded as file using the "Download" button or used for copy/paste from the text window below.
Citation data in RIS format can be imported by all major citation management software, including EndNote, ProCite, RefWorks, and Zotero.

Presentation Graphic

Picture with graphical abstract, title and authors for social media postings and presentations.
Format: PNG Size: 160.9 KB Download

Citations to This Article

Up to 20 of the most recent references are displayed here.

Scholarly Works

  • Kis, P.; Horváthová, E.; Gálová, E.; Ševčovičová, A.; Antalová, V.; Karnišová Potocká, E.; Mastihuba, V.; Mastihubová, M. Synthesis of Tyrosol and Hydroxytyrosol Glycofuranosides and Their Biochemical and Biological Activities in Cell-Free and Cellular Assays. Molecules (Basel, Switzerland) 2021, 26, 7607. doi:10.3390/molecules26247607
  • Kis, P.; Mastihubová, M. A sustainable approach to phenylethanoid glycopyranosides: Study of glycosylations promoted by zinc salts. Sustainable Chemistry and Pharmacy 2021, 24, 100537. doi:10.1016/j.scp.2021.100537
  • Dong, H.; Du, W.; Zhongquan, Y.; Wu, M.; Hongbing, L.; He, Y.; Cao, S. First total syntheses of two natural glycosides. Carbohydrate research 2020, 499, 108200. doi:10.1016/j.carres.2020.108200
  • Horváthová, E.; Mastihubová, M.; Potocká, E. K.; Kis, P.; Gálová, E.; Sevcovicova, A.; Klapakova, M.; Hunakova, L.; Mastihuba, V. Comparative study of relationship between structure of phenylethanoid glycopyranosides and their activities using cell-free assays and human cells cultured in vitro. Toxicology in vitro : an international journal published in association with BIBRA 2019, 61, 104646. doi:10.1016/j.tiv.2019.104646
  • Liu, D.-K.; Xiong, D.-C.; Wu, X.; Li, Q.; Ye, X.-S. Rapid glycosylation of 2′-benzoylphenyl glycosides promoted by TfOH. Organic Chemistry Frontiers 2019, 6, 2756–2759. doi:10.1039/c9qo00629j
  • Begum, A. S.; Kumar, S.; Gottapu, S.; Hira, K. O-Glucoside of natural cleomiscosin-A: An attenuator of pro-inflammatory cytokine production. Phytochemistry Letters 2018, 26, 83–87. doi:10.1016/j.phytol.2018.05.022
  • Kulkarni, S. S.; Wang, C.-C.; Sabbavarapu, N. M.; Podilapu, A. R.; Liao, P.-H.; Hung, S.-C. "One-Pot" Protection, Glycosylation, and Protection-Glycosylation Strategies of Carbohydrates. Chemical reviews 2018, 118, 8025–8104. doi:10.1021/acs.chemrev.8b00036
  • Khong, D. T.; Judeh, Z. M. A. Total synthesis of phenylpropanoid glycoside osmanthuside-B6 facilitated by double isomerisation of glucose–rhamnose orthoesters. Organic & biomolecular chemistry 2017, 15, 2638–2646. doi:10.1039/c7ob00198c
  • Chen, J.; Lu, F.; Si, X.; Nie, X.; Chen, J.; Lu, R.; Xu, J. High Yield Production of Natural Phenolic Alcohols from Woody Biomass Using a Nickel-Based Catalyst. ChemSusChem 2016, 9, 3353–3360. doi:10.1002/cssc.201601273
Other Beilstein-Institut Open Science Activities