1,5-ANHYDRO-4-O-[3,4-BIS-O-(TERT.-BUTYLDIPHENYLSILYL)-6-DEOXY-2-PHENYLSELENO-BETA-GLUCO-PYRANOSYL]-2,6-DIDEOXY-L-ERYTHRO-HEX-1-EN-3-ULOSE
Compound with spectra: 1 NMR
![1,5-ANHYDRO-4-O-[3,4-BIS-O-(TERT.-BUTYLDIPHENYLSILYL)-6-DEOXY-2-PHENYLSELENO-BETA-GLUCO-PYRANOSYL]-2,6-DIDEOXY-L-ERYTHRO-HEX-1-EN-3-ULOSE](/api/compound/I8k1w7ws5kn.png?ph=true&h=300&w=458 "1,5-ANHYDRO-4-O-[3,4-BIS-O-(TERT.-BUTYLDIPHENYLSILYL)-6-DEOXY-2-PHENYLSELENO-BETA-GLUCO-PYRANOSYL]-2,6-DIDEOXY-L-ERYTHRO-HEX-1-EN-3-ULOSE")
| SpectraBase Compound ID | I8k1w7ws5kn |
|---|---|
| InChI | InChI=1S/C50H58O6SeSi2/c1-36-44(43(51)34-35-52-36)54-48-47(57-38-24-14-9-15-25-38)46(56-59(50(6,7)8,41-30-20-12-21-31-41)42-32-22-13-23-33-42)45(37(2)53-48)55-58(49(3,4)5,39-26-16-10-17-27-39)40-28-18-11-19-29-40/h9-37,44-48H,1-8H3/t36-,37-,44-,45-,46+,47-,48+/m1/s1 |
| InChIKey | JIRUEVDLNJUEOZ-XEKMOPKXSA-N |
| Mol Weight | 890.1 g/mol |
| Molecular Formula | C50H58O6SeSi2 |
| Exact Mass | 890.293715 g/mol |
| Enantiomer InChIKey | JIRUEVDLNJUEOZ-RJTUDNHYSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | C6D6 |
1,5-ANHYDRO-4-O-[3,4-BIS-O-(TERT.-BUTYLDIMETHYLSILYL)-6-DEOXY-2-PHENYLSELENO-BETA-L-GLUCOPYRANOSYL]-L-RIBO-HEX-1-ENITOL
1,5-ANHYDRO-4-O-[3,4-BIS-O-(TERT.-BUTYLDIPHENYLSILYL)-6-DEOXY-2-PHENYLSELENO-BETA-L-GLUCO-PYRANOSYL]-L-ARABINO-HEX-1-ENITOL
1,5-ANHYDRO-4-O-[3,4-BIS-O-(TERT.-BUTYLDIPHENILSILYL)-6-DEOXY-2-PHETA-L-GLUCO-PYRANOSYL]-3-O-(TERT.-BUTYLDIMETHYLSILIL)-2,6-DIDEOXY-L-ARABINO-HEX-1
4-C-(BENZOYLOXYMETHYL)-3,5-DI-O-(TERT.-BUTYLDIPHENYLSILYL)-1,2-O-ISOPROPYLIDENE-ALPHA-D-XYLOFURANOSIDE
METHYL-2,4-DI-O-BENZOYL-6-O-(TERT.-BUTYLDIPHENYLSILYL)-BETA-D-GALACTOPYRANOSYL-(1->4)-2,3,6-TRI-O-BENZOYL-ALPHA-D-MANNOPYRANOSIDE
#31;BENZYL-O-[2-O-BENZOYL-4,6-O-[(S)-1-(METHOXYCARBONYL)-ETHYLIDENE]-3-O-METHYL-BETA-D-GLUCOPYRANOSYL]-(1->3)-2-O-BENZOYL-4,6-O-[(S)-1-(METHOXYCARBONYL)-ETHYLI
4-BENZYL-9B-METHOXY-9-METHYL-3,4,8,9,9A,9B-HEXAHYDRO-PYRAZOLO-[3,4-H]-[1,4]-BENZOXAZIN-6(2H)-ONE
BIOSIDE 5 (FROM PSEUDOMONAS AERUGINOSA O)
BIOSIDE 4 (FROM PSEUDOMONAS AERUGINOSA O)
BIOSIDE 3
| Title | Journal or Book | Year |
|---|---|---|
| Simple oxidation of 3-O-silylated glycals: application in deblocking 3-O-protected glycals | Journal of the Chemical Society, Perkin Transactions 1 | 1999 |