2,2-DIPHENYL-5-[(E)-HEPT-1-EN-1-YL]-4-[(TERT.-BUTYLDIMETHYLSILYLOXY)-METHYL]-OXAZOLIDINE
Compound with spectra: 1 NMR
![2,2-DIPHENYL-5-[(E)-HEPT-1-EN-1-YL]-4-[(TERT.-BUTYLDIMETHYLSILYLOXY)-METHYL]-OXAZOLIDINE](/api/compound/9G0Q4ve9Ljy.png?ph=true&h=300&w=458 "2,2-DIPHENYL-5-[(E)-HEPT-1-EN-1-YL]-4-[(TERT.-BUTYLDIMETHYLSILYLOXY)-METHYL]-OXAZOLIDINE")
| SpectraBase Compound ID | 9G0Q4ve9Ljy |
|---|---|
| InChI | InChI=1S/C29H43NO2Si/c1-7-8-9-10-17-22-27-26(23-31-33(5,6)28(2,3)4)30-29(32-27,24-18-13-11-14-19-24)25-20-15-12-16-21-25/h11-22,26-27,30H,7-10,23H2,1-6H3/b22-17+ |
| InChIKey | LCWGJOZOGOZCNF-OQKWZONESA-N |
| Mol Weight | 465.8 g/mol |
| Molecular Formula | C29H43NO2Si |
| Exact Mass | 465.306306 g/mol |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
2,2-DIPHENYL-5-[(E)-DEC-1-EN-1-YL]-4-[(TERT.-BUTYLDIMETHYLSILYLOXY)-METHYL]-OXAZOLIDINE
2,2-DIPHENYL-5-[(E)-HEX-1-EN-1-YL]-4-[(TERT.-BUTYLDIMETHYLSILYLOXY)-METHYL]-OXAZOLIDINE
(5S,6R)-1-Benzyl-5-benzyloxy-6-(tert-butyldimethylsilyloxymethyl)-5,6-dihydro-1H-pyridin-2-one
2,3-DIHYDRO-2,2-DIPHENYL-4H-1,3-BENZOXAZIN-4-ONE
(1RS,6SR)-2-Aza-7-oxa-8,8-diphenylbicyclo[4.2.0]octan-3-one
(-)-(4R,5R)-4-Hydroxy-4-(hydroxymethyl)-5-[(1E)-1-(triphenylmethoxymethyl)-1,3-butadienyl]-2-cyclopentenone
(-)-(4R,5S)-4-Hydroxy-4-(hydroxymethyl)-5-[(1E)-1-(triphenylmethoxymethyl)-1,3-butadienyl]-2-cyclopentenone
(E,4S)-1-[(4S,5S)-5-[[tert-butyl(dimethyl)silyl]oxymethyl]-2,2-dimethyl-1,3-dioxolan-4-yl]-4-[tert-butyl(diphenyl)silyl]oxy-1-penten-3-one
H-ASN(MTT)-THR(TBU)-PNAH-ASPARAGINE(MTT)-THREONINE(TBU)-PARANITROANILINE
(5S)-1-[(Z,3R)-3-[dimethyl(phenyl)silyl]-1-oxohexadec-4-enyl]-5-[(triphenylmethyl)oxymethyl]-2-pyrrolidinone
| Title | Journal or Book | Year |
|---|---|---|
| Aluminoxy acetals from .alpha.-amino esters: chirality transfer via sequential addition of hydride and C-nucleophiles. 2-Amino alcohols and sphingosines | The Journal of Organic Chemistry | 1992 |