(2S)-METHYL-4-[(3S,4R,5R,6R)-4,5-BIS-(BENZYLOXY)-6-(BENZYLOXYMETHYL)-3-HYDROXYTETRAHYDRO-2H-PYRAN-2-YL]-2-(TERT.-BUTOXYCABONYLAMINO)-BUTANOATE
Compound with spectra: 1 NMR
![(2S)-METHYL-4-[(3S,4R,5R,6R)-4,5-BIS-(BENZYLOXY)-6-(BENZYLOXYMETHYL)-3-HYDROXYTETRAHYDRO-2H-PYRAN-2-YL]-2-(TERT.-BUTOXYCABONYLAMINO)-BUTANOATE](/api/compound/Cz5aavqW7Wy.png?ph=true&h=300&w=458 "(2S)-METHYL-4-[(3S,4R,5R,6R)-4,5-BIS-(BENZYLOXY)-6-(BENZYLOXYMETHYL)-3-HYDROXYTETRAHYDRO-2H-PYRAN-2-YL]-2-(TERT.-BUTOXYCABONYLAMINO)-BUTANOATE")
| SpectraBase Compound ID | Cz5aavqW7Wy |
|---|---|
| InChI | InChI=1S/C37H47NO9/c1-37(2,3)47-36(41)38-29(35(40)42-4)20-21-30-32(39)34(45-24-28-18-12-7-13-19-28)33(44-23-27-16-10-6-11-17-27)31(46-30)25-43-22-26-14-8-5-9-15-26/h5-19,29-34,39H,20-25H2,1-4H3,(H,38,41)/t29-,30+,31+,32-,33+,34+/m0/s1 |
| InChIKey | YHMVMSMQHJWMSO-JYDMMBCBSA-N |
| Mol Weight | 649.8 g/mol |
| Molecular Formula | C37H47NO9 |
| Exact Mass | 649.325082 g/mol |
| Enantiomer InChIKey | YHMVMSMQHJWMSO-BFVJSROOSA-N |
| Copyright | Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(2R,3R,4R,4ar,8as)-3-Benzyloxy-2-(benzyloxymethyl)octahydropyrano[3,2-B]pyran-4-yl 4-nitrobenzoate
PHENYL 3,4,6-TRI-O-BENZYL-1-THIO-ALPHA-D-MANNOPYRANOSIDE
1-DEOXY-1-C-PHENYL-2,3,4,6-TETRA-O-BENZYL-BETA-D-GLUCOPYRANOSE
1-DEOXY-1-C-PHENYL-2,3,4,6-TETRA-O-BENZYL-ALPHA-D-GLUCOPYRANOSE
ALPHA-1,5-ANHYDRO-1-C-PHENYL-2,3,4,6-TETRA-O-BENZYL-D-GLUCITOL
2,3,4,6-TETRA-O-BENZYL-ALPHA-D-GLUCOPYRANOSYL-AZIDE
o-(2,3,4,6-Tetra-o-benzyl-alpha-D-mannopyranosyl)-o,o-diethylphosphite
2,3,4,6-TETRA-O-BENZYL-ALPHA-D-MANNOPYRANOSYLPHOSPHITE,TRIETHYLAMMONIUM SALT
1-O-(4-NITROPHENYL)-2,3,4,6-TETRA-O-BENZYL-ALPHA-D-GLUCOPYRANOSIDE
1-O-(4-BROMOPHENYL)-2,3,4,6-TETRA-O-BENZYL-ALPHA-D-GLUCOPYRANOSIDE
| Title | Journal or Book | Year |
|---|---|---|
| Stereoselective Synthesis of α-C-Glucosyl Serine and Alanine via a Cross-Metathesis/Cyclization Strategy | Organic Letters | 2005 |