ANTI-5-CARBOMETHOXY-5-[1'-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-BUTYL]-3-PHENYL-4,5-DIHYDROISOXAZOLE;MINOR_STEREOMER
Compound with spectra: 1 NMR
![ANTI-5-CARBOMETHOXY-5-[1'-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-BUTYL]-3-PHENYL-4,5-DIHYDROISOXAZOLE;MINOR_STEREOMER](/api/compound/3UMIUjtF3J1.png?ph=true&h=300&w=458 "ANTI-5-CARBOMETHOXY-5-[1'-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-BUTYL]-3-PHENYL-4,5-DIHYDROISOXAZOLE;MINOR_STEREOMER")
| SpectraBase Compound ID | 3UMIUjtF3J1 |
|---|---|
| InChI | InChI=1S/C21H33NO4Si/c1-8-12-18(25-27(6,7)20(2,3)4)21(19(23)24-5)15-17(22-26-21)16-13-10-9-11-14-16/h9-11,13-14,18H,8,12,15H2,1-7H3/t18-,21+/m1/s1 |
| InChIKey | NILLRRKZJMGJCM-NQIIRXRSSA-N |
| Mol Weight | 391.6 g/mol |
| Molecular Formula | C21H33NO4Si |
| Exact Mass | 391.217885 g/mol |
| Enantiomer InChIKey | NILLRRKZJMGJCM-GHTZIAJQSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
SYN-5-CARBOMETHOXY-5-[1'-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-2'-METHYLPROPYL]-3-PHENYL-4,5-DIHYDROISOXAZOLE;MAJOR_STEREOMER
ANTI-5-CARBOMETHOXY-5-[1'-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-2'-METHYLPROPYL]-3-PHENYL-4,5-DIHYDROISOXAZOLE;MINOR_STEREOMER
3-(2,4,6-TRIMETHYLPHENYL)-8-PHENYL-6-OXO-1,7-DIOXA-2-AZA-SPIRO-[4.4]-NON-2-ENE
(E)-5-Fluoro-3'-phenyl-4'-hydrospiro[adamantane-2:5'-.delta.-(2)-isoxazoline]
ENDO-METHYL-(2E)-3-[5-[4-(TRIFLUOROMETHYL)-PHENYL]-3-OXA-4-AZATRICYCLO-[5.2.1.0(2,6)]-DEC-4-EN-9-YL]-PROP-2-ENOATE
(3R*,4R*)-3-(3,4-Methylenedioxybenzyl)-4-[.alpha.(S)-.alpha.-trimethylsilyloxy-3,4-dimethoxybenzyl]-.gamma.-butyrolactone
ANTI-1-METHYL-3,8-DIPHENYL-7-OXA-1,2-DIAZASPIRO-[4.4]-NON-2-EN-6-ONE
SYN-1-METHYL-3,8-DIPHENYL-7-OXA-1,2-DIAZASPIRO-[4.4]-NON-2-EN-6-ONE
(1R*,9S*)-3-(TERT.-BUTYLDIMETHYLSILYLOXY)-8,8-DIMETHYL-TRICYCLO-[7.3.0.0(2,7)]-DODEC-2(7)-ENE
| Title | Journal or Book | Year |
|---|---|---|
| 1,3-Dipolar Cycloadditions to Baylis-Hillman Adducts: Rationale for the Observed Diastereoselectivity | The Journal of Organic Chemistry | 1995 |