JMSZJUCNLNWISV-ZGXWSNOMSA-N
Compound with spectra: 1 NMR
| SpectraBase Compound ID | HPVsg7xIt6M |
|---|---|
| InChI | InChI=1S/C21H25NO9/c1-12(23)28-11-17-19(30-14(3)25)20(31-15(4)26)18(29-13(2)24)10-22(17)21(27)16-8-6-5-7-9-16/h5-9,17-20H,10-11H2,1-4H3/t17-,18+,19-,20+/m0/s1 |
| InChIKey | JMSZJUCNLNWISV-ZGXWSNOMSA-N |
| Mol Weight | 435.43 g/mol |
| Molecular Formula | C21H25NO9 |
| Exact Mass | 435.152931 g/mol |
| Enantiomer InChIKey | JMSZJUCNLNWISV-WCIQWLHISA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
6-ACETAMIDO-2,3,4-TRI-O-ACETYL-1,6-ANHYDRO-6-DEOXY-BETA-D-GLUCOPYRANOSE;MAJOR-ROTAMER
N-ACETYL-N-PROP-2-YNYL-2,3,4,6-TETRA-O-ACETYL-ALPHA-D-MANNOPYRANOSYLAMINE
(1R,2S,7R,8R,8AS)-1,2,7,8-TETRAACETOXYINDOLIZIDIN-5-ONE
(1R,2S,7S,8S,8AS)-1,2,7,8-TETRAACETOXYINDOLIZIDIN-5-ONE
FXWURHPTBVHABM-BGSSSCFASA-N
TERT.-BUTYL_N-[2-OXO-2-[(3,4,6-TRI-O-ACETYL-2-ACETAMINO-2-DEOXY-BETA-D-GLUCOPYRANOSYL)-AMINO]-ETHYL]-GLYCYLGLYCINATE
O-(2,3,4,6-TETRA-O-ACETYL-1,5-DIDEOXY-1,5-IMINO-D-GLUCOPYRANOSYLIDENE)-AMINO-N-(2-CHLOROPHENYL)-CARBAMATE
N(ALPHA)-(TERT.-BUTOXYCARBONYL)-O-(2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSYL)-L-SERINE-BENZYLESTER
N-ACETYL-3-O-(2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-ALPHA-D-GALACTOPYRANOSYL)-L-SERINE-(N'-BENZYLOXYCARBONYLAMINOETHYL)-AMIDE
| Title | Journal or Book | Year |
|---|---|---|
| An Oxidative Mannich Cyclization Methodology for the Stereocontrolled Synthesis of Highly Functionalized Piperidines | The Journal of Organic Chemistry | 1998 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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