Addition of lithiated enol ethers to nitrones and subsequent Lewis acid induced cyclizations to enantiopure 3,6-dihydro-2H-pyrans – an approach to carbohydrate mimetics

Fabian Pfrengle and Hans-Ulrich Reissig
Beilstein J. Org. Chem. 2010, 6, No. 75. https://doi.org/10.3762/bjoc.6.75

Supporting Information

Supporting Information File 1: Experimental procedures, characterization data, 1H NMR and 13C NMR spectra of synthesized compounds.
Format: PDF Size: 3.1 MB Download

Cite the Following Article

Addition of lithiated enol ethers to nitrones and subsequent Lewis acid induced cyclizations to enantiopure 3,6-dihydro-2H-pyrans – an approach to carbohydrate mimetics
Fabian Pfrengle and Hans-Ulrich Reissig
Beilstein J. Org. Chem. 2010, 6, No. 75. https://doi.org/10.3762/bjoc.6.75

How to Cite

Pfrengle, F.; Reissig, H.-U. Beilstein J. Org. Chem. 2010, 6, No. 75. doi:10.3762/bjoc.6.75

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.

Citations to This Article

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

Scholarly Works

  • Salta, J.; Reissig, H.-U. Divalent Triazole‐Linked Carbohydrate Mimetics: Synthesis by Click Chemistry and Evaluation as Selectin Ligands. European Journal of Organic Chemistry 2020, 2020, 4361–4370. doi:10.1002/ejoc.202000618
  • Pfrengle, F.; Reissig, H.-U. Internally Protected Amino Sugar Equivalents from Enantiopure 1,2‐Oxazines: Synthesis of Variably Configured Carbohydrates with C‐Branched Amino Sugar Units. Chemistry (Weinheim an der Bergstrasse, Germany) 2010, 16, 11915–11925. doi:10.1002/chem.201001060
Other Beilstein-Institut Open Science Activities