#14;(+/-)-2-EXO-(TERT.-BUTYL-DIPHENYL-SILANYLOXY)-3-ENDO-ACETYL-6-EXO-ACETOXYMETHYL-7-OXA-BICYCLO-[2.2.1]-HEPTAN-5-YLCARBOXALDEHYDE-1,1-DIMETHYLHYDRAZONE
Compound with spectra: 1 NMR
![#14;(+/-)-2-EXO-(TERT.-BUTYL-DIPHENYL-SILANYLOXY)-3-ENDO-ACETYL-6-EXO-ACETOXYMETHYL-7-OXA-BICYCLO-[2.2.1]-HEPTAN-5-YLCARBOXALDEHYDE-1,1-DIMETHYLHYDRAZONE](/api/compound/7p5FWCTKvvl.png?ph=true&h=300&w=458 "#14;(+/-)-2-EXO-(TERT.-BUTYL-DIPHENYL-SILANYLOXY)-3-ENDO-ACETYL-6-EXO-ACETOXYMETHYL-7-OXA-BICYCLO-[2.2.1]-HEPTAN-5-YLCARBOXALDEHYDE-1,1-DIMETHYLHYDRAZONE")
| SpectraBase Compound ID | 7p5FWCTKvvl |
|---|---|
| InChI | InChI=1S/C30H40N2O6Si/c1-20(33)35-19-25-24(18-31-32(6)7)26-28(36-21(2)34)29(27(25)37-26)38-39(30(3,4)5,22-14-10-8-11-15-22)23-16-12-9-13-17-23/h8-18,24-29H,19H2,1-7H3/b31-18+/t24-,25-,26+,27-,28-,29-/m0/s1 |
| InChIKey | MVEMWNHHRNTERC-AWINSQKBSA-N |
| Mol Weight | 552.7 g/mol |
| Molecular Formula | C30H40N2O6Si |
| Exact Mass | 552.265564 g/mol |
| Enantiomer InChIKey | MVEMWNHHRNTERC-WRLQEZHISA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(+/-)-2-EXO-(TERT.-BUTYL-DIPHENYL-SILANYLOXY)-5-OXO-4,8-DIOXA-TRICYCLO-[4.2.1.0(3,7)]-NONAN-9-EXO-CARBOXYLIC-ACID
No Name
#B5;1,13-BIS-[4-[2-ACETAMIDO-3,6-DI-O-ACETYL-2-DEOXY-4-O-(2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSYL)-BETA-D-GLUCOPYRANOSYL-OXYMETHYL]
D-Glucitol, 1-[acetyl(4-benzoylphenyl)amino]-1-deoxy-4-O-(2,3,4,6-tetra-O-acetyl- .beta.-D-galactopyranosyl)-, 2,3,5,6-tetraacetate
(1R,2S,3S,4S,5S)-2-ACETOXY-1-AZIDO-3-(TERT.-BUTYLDIPHENYLSILYLOXY)-4,5-DIHYDROXYCYCLOHEX-5-YL-METHYL-ACETATE
(1S,2S,3S,4S,5S)-2-ACETOXY-1-AZIDO-3-(TERT.-BUTYLDIPHENYLSILYLOXY)-4,5-DIHYDROXYCYCLOHEX-5-YL-METHYL-ACETATE
CALEIN-D
ARUCANOLIDE
Arucanolide A
(1R,2S,3R,4R)-1-(5-AMINO-4-CARBAMOYL-1H-1,2,3-TRIAZOL-1-YL)-2,3-ISOPROPYLIDENE-DIOXY-4-[(TERT.-BUTYLDIPHENYLSILYLOXY)-METHYL]-CYCLOPENTANE
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis of a Carbasugar Analogue of a Putative Intermediate in the UDP-Galp-Mutase Catalyzed Isomerization | Organic Letters | 2005 |