(2R*,5R*,6R*)-3-(TERT.-BUTYLDIMETHYLSILOXY)-5-(TRIMETHYLSILYL)-6-FORMYL-5,6,7,8-TETRAHYDRO-2H-OXOCINE-2-CARBOXYLIC-ACID-METHYLESTER
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 6w8ThfxgWHY |
|---|---|
| InChI | InChI=1S/C19H36O5Si2/c1-19(2,3)26(8,9)24-15-12-16(25(5,6)7)14(13-20)10-11-23-17(15)18(21)22-4/h12-14,16-17H,10-11H2,1-9H3/b15-12+/t14-,16-,17-/m0/s1 |
| InChIKey | DCAMYGIAYKWVGS-HGUGKSJVSA-N |
| Mol Weight | 400.7 g/mol |
| Molecular Formula | C19H36O5Si2 |
| Exact Mass | 400.210127 g/mol |
| Enantiomer InChIKey | DCAMYGIAYKWVGS-QGTZPMKFSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(1-R*,4-R*,5-R*)-2-(TERT.-BUTYLDIMETHYLSILOXY)-5-FORMYL-4-(TRIMETHYLSILYL)-CYCLOOCT-2-ENECARBOXYLIC_ACID_METHYLESTER
4-TERT.-BUTYL-2-(TERT.-BUTYLDIMETHYLSILOXY)-BICYCLO-[3.3.2]-DEC-2-EN-9-ONE
METHYL-(1S,5R)-3-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-1,5-DIHYDROXY-4-OXOCYCLOHEX-2-ENECARBOXYLATE
2,3,4,5-TETRA-O-ACETYL-6-O-(TERT.-BUTYLDIMETHYLSILYL)-1-O-(PARA-TOLUENESULFONYL)-D-MANNITOL
tert-Butyl-dimethyl-[[(1S,4R,5R)-3-triethylsilyloxy-8-oxabicyclo[3.2.1]octa-2,6-dien-4-yl]oxy]silane
(1'S)-2-(1'-Phenylethoxy)-3-(triethylsilyloxy)-8-oxa-bicyclo[3.2.1]oct-3,6-diene
1,2:5,6-Di-isopropylidene-4-O-(prop-1,2-dienyl)-3-O-(tert-butyldimethylsilyl)-D-mannofuranose
3-[(Benzoyloxy)methyl]-5-(tert-butyldiphenylsilyl)-3-deoxy-1-O-methylribofuranose
Gluconolactone (3R,4S,5R,6R)- 4TMS
Decahydro-7-.beta.-[(tert-butyldimethylsilyl)oxy]-6,6,9a.beta.-trimethyl-2-oxo-1-benzoxepin
| Title | Journal or Book | Year |
|---|---|---|
| Stereoselective Construction of Eight-Membered Oxygen Heterocycles by Brook Rearrangement-Mediated [3 + 4] Annulation | Organic Letters | 2004 |
KnowItAll NMR Spectral Library
Author: Wiley
The KnowItAll NMR Spectral Library offers a comprehensive collection of NMR reference spectra, including NMR, CNMR, and XNMR, and covers a wide range of compounds including organics, polymers, monomers, metabolites, and more. Learn more.