#13;METHYL-4,6-O-BENZYLIDENE-3-O-[BIS-(ALPHA,ALPHA,ALPHA,ALPHA',ALPHA',ALPHA'-HEXAFLUORO-3,5-XYLYL)-PHOSPHINO]-2-DEOXY-2-(ETHYLAMINO)-BETA-D-GLUCOPYRANOSIDE
Compound with spectra: 1 NMR
![#13;METHYL-4,6-O-BENZYLIDENE-3-O-[BIS-(ALPHA,ALPHA,ALPHA,ALPHA',ALPHA',ALPHA'-HEXAFLUORO-3,5-XYLYL)-PHOSPHINO]-2-DEOXY-2-(ETHYLAMINO)-BETA-D-GLUCOPYRANOSIDE](/api/compound/CcTdmuH5zc7.png?ph=true&h=300&w=458 "#13;METHYL-4,6-O-BENZYLIDENE-3-O-[BIS-(ALPHA,ALPHA,ALPHA,ALPHA',ALPHA',ALPHA'-HEXAFLUORO-3,5-XYLYL)-PHOSPHINO]-2-DEOXY-2-(ETHYLAMINO)-BETA-D-GLUCOPYRANOSIDE")
| SpectraBase Compound ID | CcTdmuH5zc7 |
|---|---|
| InChI | InChI=1S/C32H28F12NO5P/c1-3-45-24-26(25-23(48-28(24)46-2)15-47-27(49-25)16-7-5-4-6-8-16)50-51(21-11-17(29(33,34)35)9-18(12-21)30(36,37)38)22-13-19(31(39,40)41)10-20(14-22)32(42,43)44/h4-14,23-28,45H,3,15H2,1-2H3/t23-,24-,25-,26-,27-,28-/m0/s1 |
| InChIKey | SFJSVFWNMNYJEK-QUQVWLGBSA-N |
| Mol Weight | 765.5 g/mol |
| Molecular Formula | C32H28F12NO5P |
| Exact Mass | 765.151348 g/mol |
| Enantiomer InChIKey | SFJSVFWNMNYJEK-BXZOIBFVSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
METHYL-2-ACETAMIDO-4,6-O-BENZYLIDENE-2-DEOXY-3-O-(DI-3,5-XYLYLPHOSPPHINO)-BETA-D-GLUCOPYRANOSIDE
BENZYL-4,6-O-BENZYLIDENE-2-DEOXY-2-(DIMETHYLAMINO)-3-O-(DI-3,5-XYLYLPHOSPPHINO)-ALPHA-D-GLUCOPYRANOSIDE
2-METHYL-4,5-(4,6-O-BENZYLIDENE-3-O-(DIPHENYLPHOSPHINO)-1,2-DIDEOXY-ALPHA-D-GLUCOPYRANO)-[2,1-D]-2-OXAZOLINE
CYCLOHEHYL-DERIVATIVE
IVDPSMIYQGDQBI-WTIZSLLQSA-N
(2S)-2-HYDROXY-2-METHYL-3-TOSYLOXYPROPYL-2-ACETAMIDO-3-O-BENZYL-4,6-O-(R)-BENZYLIDENE-2-DEOXY-BETA-D-GLUCOPYRANOSIDE
BIS-1,11-[2-ACETAMIDO-3-O-BENZYL-4,6-O-BENZYLIDENE-2-DEOXY-BETA-D-GLUCOPYRANOSYL]-(6-TOSYL-3,9-DIOXA-6-AZA-UNDECANE)
1-HEXYL-DERIVATIVE
YZIGUQVZBODXCZ-VBYLYSNGSA-N
METHYL-2-N,N-DIBENZYLAMINO-3-O-BENZOYL-4,6-O-BENZYLIDENE-2-DEOXY-ALPHA-D-GLUCOPYRANOSIDE
| Title | Journal or Book | Year |
|---|---|---|
| Tunable Ligands for Asymmetric Catalysis: Readily Available Carbohydrate-Derived Diarylphosphinites Induce High Selectivity in the Hydrovinylation of Styrene Derivatives | Journal of the American Chemical Society | 2001 |