SYN-5-CARBOMETHOXY-5-[1'-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-1'-PHENYLMETHYL]-3-PHENYL-4,5-DIHYDROISOXAZOLE;MAJOR_STEREOMER
Compound with spectra: 1 NMR
![SYN-5-CARBOMETHOXY-5-[1'-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-1'-PHENYLMETHYL]-3-PHENYL-4,5-DIHYDROISOXAZOLE;MAJOR_STEREOMER](/api/compound/3FZYrvoCQLO.png?ph=true&h=300&w=458 "SYN-5-CARBOMETHOXY-5-[1'-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-1'-PHENYLMETHYL]-3-PHENYL-4,5-DIHYDROISOXAZOLE;MAJOR_STEREOMER")
| SpectraBase Compound ID | 3FZYrvoCQLO |
|---|---|
| InChI | InChI=1S/C24H31NO4Si/c1-23(2,3)30(5,6)28-21(19-15-11-8-12-16-19)24(22(26)27-4)17-20(25-29-24)18-13-9-7-10-14-18/h7-16,21H,17H2,1-6H3/t21-,24+/m1/s1 |
| InChIKey | MZGPUIBKGKRKPD-QPPBQGQZSA-N |
| Mol Weight | 425.6 g/mol |
| Molecular Formula | C24H31NO4Si |
| Exact Mass | 425.202235 g/mol |
| Enantiomer InChIKey | MZGPUIBKGKRKPD-XUZZJYLKSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
Benzyl-dehydro-ascorbic acid, methyl glucoside
Methyl 2-(cyclohexylmethyl)-3-((1,1-dimethylethyl)diphenylsilyloxy)-3-(1-naphthyl)propanoate (2:1 anti/syn mixture)
3-(4',4'-Dimethyl-2'-oxazolin-2'-yl)-3,4-epoxy-2-methyl-4,4-diphenyl-2-butanol
3-Phenyl-spiro[2"-(1-oxo-5-methoxytetrahydro)naphthalene]-5-isoxazoline
3a,8a-Propano-4H-cyclohept[d]isoxazol-4-one, 5,6,7,8-tetrahydro-3-phenyl-
S-Phenyl (2RS,3R)-3-(tert-butyldimethylsiloxy)-3-phenyl-2-phthalimidopropanethioate
3-(2,6-DICHLOROPHENYL)-7-(3,5-DICHLOROPHENYL)-6,8-DIOXO-1-OXA-2,7-DIAZA-SPIRO-[4,4]-NON-2-ENE
Trimipramine-M (nor-di-HO-) 3AC
3-benzofurancarboxylic acid, 5-[acetyl[(4-chlorophenyl)sulfonyl]amino]-2-methyl-, methyl ester
| Title | Journal or Book | Year |
|---|---|---|
| 1,3-Dipolar Cycloadditions to Baylis-Hillman Adducts: Rationale for the Observed Diastereoselectivity | The Journal of Organic Chemistry | 1995 |