(2S,3S,4S,5R)-3,4,5-TRIACETOXY-2-[N-METHYL-N-(DIPHENYLMETHYL)-AMINO]-1-O-(TERT.-BUTYLDIMETHYLSILYL)-HEXAN-1-OL
Compound with spectra: 1 NMR
![(2S,3S,4S,5R)-3,4,5-TRIACETOXY-2-[N-METHYL-N-(DIPHENYLMETHYL)-AMINO]-1-O-(TERT.-BUTYLDIMETHYLSILYL)-HEXAN-1-OL](/api/compound/1Wkw3NpWMlB.png?ph=true&h=300&w=458 "(2S,3S,4S,5R)-3,4,5-TRIACETOXY-2-[N-METHYL-N-(DIPHENYLMETHYL)-AMINO]-1-O-(TERT.-BUTYLDIMETHYLSILYL)-HEXAN-1-OL")
| SpectraBase Compound ID | 1Wkw3NpWMlB |
|---|---|
| InChI | InChI=1S/C32H47NO7Si/c1-22(38-23(2)34)30(39-24(3)35)31(40-25(4)36)28(21-37-41(9,10)32(5,6)7)33(8)29(26-17-13-11-14-18-26)27-19-15-12-16-20-27/h11-20,22,28-31H,21H2,1-10H3/t22-,28+,30-,31+/m0/s1 |
| InChIKey | OCSWWCZAFQOGEC-IOYLGXLSSA-N |
| Mol Weight | 585.8 g/mol |
| Molecular Formula | C32H47NO7Si |
| Exact Mass | 585.312179 g/mol |
| Enantiomer InChIKey | OCSWWCZAFQOGEC-UAANJTJOSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(3R,4R,5R,6R)-3,4,5-Triacetoxy-2-(tert-butyldimethylsilyloxymethyl)-6-oxopiperidine
N-(7-OXADECYL)-2,3,4-TRI-O-ACETYL-6-O-BENZYL-1,5-DIDEOXY-1,5-IMINO-D-GLUCITOL
N-(7-OXADECYL)-2,3,4,6-TETRA-O-ACETYL-1,5-DIDEOXY-1,5-IMINO-D-GLUCITOL
1-O-ACETYL-3-(BENZYLAMINO)-3-DEOXY-4-O-(HYDROXYACETYL)-D-GLYCERO-D-GALACTO-HEPTITOL
N-BENZYL-OXYCARBONYL-N-[3,4,6-TRI-O-ACETYL-1,5-ANHYDRO-2-DEOXY-GLUCITOL-2]-2-ASPARAGINE-BENZYLESTER
2,3,4,6-TETRA-O-ACETYL-D-GLUCONHYDROXIMO-1,5-LACTAM
2-N-BENZHYDRYL-2,6-DIDEOXY-2,6-IMINO-3,4-O-ISOPROPYLIDENE-D-ALLONONITRILE
1,2,3,4,6-PENTA-O-ACETYL-5-ACETYLAMINO-5,7,8,9-TETRADEOXY-D-GLYCERO-D-GALACTO-8-NONENITOL
1,4,5-Tri-o-acetyl-3,6-di-o-methyl-2-n-methylacetamido-2-deoxyhexitol (1-d)
Allyl-3,4,6-tri-O-acetyl-2-acetylamino-2-deoxy-b-d-glucopyranoside
| Title | Journal or Book | Year |
|---|---|---|
| An Enantioselective Synthesis of N-Methylfucosamine via Tandem C-C/C-O Bond Formation | The Journal of Organic Chemistry | 1994 |