3,4-DI-O-ACETYL-2,6-DIDEOXY-6-PHENYLSELENO-2-TRIFLUOROACETAMIDO-ALPHA-D-GLUCOPYRANOSYL-1-DIBENZYL-PHOSPHATE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | JTCEShrUr77 |
|---|---|
| InChI | InChI=1S/C32H33F3NO10PSe/c1-21(37)43-28-26(20-48-25-16-10-5-11-17-25)45-30(27(29(28)44-22(2)38)36-31(39)32(33,34)35)46-47(40,41-18-23-12-6-3-7-13-23)42-19-24-14-8-4-9-15-24/h3-17,26-30H,18-20H2,1-2H3,(H,36,39)/t26-,27-,28-,29-,30-/m0/s1 |
| InChIKey | QNESRJJPNFUIIO-IIZANFQQSA-N |
| Mol Weight | 758.6 g/mol |
| Molecular Formula | C32H33F3NO10PSe |
| Exact Mass | 759.09594 g/mol |
| Enantiomer InChIKey | QNESRJJPNFUIIO-XZTOTZIXSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
2-ACETAMIDO-2-DEOXY-3,4,6-TRI-O-BENZOYL-ALPHA-D-GLUCOPYRANOSYL(METHYL)PHOSPHATE, TRIETHYLAMMONIUM SALT
2-ACETAMIDO-6-O-(2-ACETAMIDO-3,4-DI-O-ACETYL-2-DEOXY-6-O-DIPHENYLPHOSPHORYL-BETA-D-GLUCOPYRANOSYL)-1,3,4-TRI-O-ACETYL-2-DEOXY-ALPHA-D-GLUCOPYRANOSE
METHYL_6-O-(2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSYL)-2,3,4-TRI-O-BENZYL-ALPHA-D-GLUCOPYRANOSIDE
3-O-ACETYL-2-O-(3,4,6-TRI-O-ACETYL-2-N-ALLYLOXYCARBONYLAMINO-2-DEOXY-BETA-D-GLUCOPYRANOSYL)-1,6-ANHYDRO-BETA-D-MANNOPYRANOSE
(2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSYL)-(1->2)-3,4-DI-O-BENZYL-L-RHAMNOPYRANOSE
4-METHYLUMBELLIFERYL-2-ACETAMIDO-2-DEOXY-3,4,6-TRI-O-ACETYL-BETA-D-GLUCOPYRANOSIDE
5-AZIDO-3-OXAPENTYL-2-ACETAMIDO-4,6-DI-O-ACETYL-2-DEOXY-3-O-(2,3,4,6-TETRA-O-ACETYL-BETA-D-GALACTOPYRANOSYL)-ALPHA-D-GALACTOPYRANOSIDE
3-O-(2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DESOXY-BETA-D-GLUCOPYRANOSYL)-1,2,4,6-TETRA-O-ACETYL-BETA-D-MANNOPYRANOSE
1A-METHYL-[2-N-ACETYL-BETA-GLUCOPYRANOSYL-(1C->3)-O-2-N-ACETYL-BETA-GLUCOPYRANOSYL-(1B->6)]-ALPHA-MANNOPYRANOSIDE
1A-METHYL-[2-N-ACETYL-BETA-GLUCOPYRANOSYL-(1C->2)-O-2-N-ACETYL-BETA-GLUCOPYRANOSYL-(1B->4)]-ALPHA-MANNOPYRANOSIDE
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis of 5-Fluoro N-Acetylglucosamine Glycosides and Pyrophosphates via Epoxide Fluoridolysis: Versatile Reagents for the Study of Glycoconjugate Biochemistry | Journal of the American Chemical Society | 2002 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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