(1R,4S,5S)-4-[(1S)-1-(TERT.-BUTYLDIPHENYLSILYLOXY)-4-PHENYL-BUT-3-ENYL]-3-OXA-6-AZA-BICYCLO-[3.1.0]-HEXAN-2-ONE
Compound with spectra: 1 NMR
![(1R,4S,5S)-4-[(1S)-1-(TERT.-BUTYLDIPHENYLSILYLOXY)-4-PHENYL-BUT-3-ENYL]-3-OXA-6-AZA-BICYCLO-[3.1.0]-HEXAN-2-ONE](/api/compound/HhGIEtuIBq9.png?ph=true&h=300&w=458 "(1R,4S,5S)-4-[(1S)-1-(TERT.-BUTYLDIPHENYLSILYLOXY)-4-PHENYL-BUT-3-ENYL]-3-OXA-6-AZA-BICYCLO-[3.1.0]-HEXAN-2-ONE")
| SpectraBase Compound ID | HhGIEtuIBq9 |
|---|---|
| InChI | InChI=1S/C30H33NO3Si/c1-30(2,3)35(23-17-9-5-10-18-23,24-19-11-6-12-20-24)34-25(28-26-27(31-26)29(32)33-28)21-13-16-22-14-7-4-8-15-22/h4-20,25-28,31H,21H2,1-3H3/b16-13+/t25-,26-,27+,28+/m0/s1 |
| InChIKey | HBGQWMYDCUNBSO-DKSBLIADSA-N |
| Mol Weight | 483.7 g/mol |
| Molecular Formula | C30H33NO3Si |
| Exact Mass | 483.22297 g/mol |
| Enantiomer InChIKey | HBGQWMYDCUNBSO-YSXZVZNTSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
3-O-[(1',1'-Dimethylethyl)diphenylsilyl]-D-talonic acid - .gamma.-lactone
(4S)-4-[(2R,4R,5R)-4-(tert-Butyldiphenylsilyloxy)-5-(5-trimethylsilylpent-2(E)-en-4-ynyl)tetrahydrofuran-2-yl]-2,2-dimethyl[[1,3]dioxolane
4,6-Dichloro-2-{[(1',1'-dimethylethyl)diphenylsilyl]oxy}-4-cyclohexene-1,3-diol - 3-acetate
4-O-Acetyl-3,6-di-O-(tert-butyldiphenylsilyl)-D-galactal
(1R,4S,5S)-6-(BENZYLOXYCARBONYL)-4-[(TERT.-BUTYLDIPHENYLSILYLOXY)-METHYL]-3-OXA-6-AZA-BICYCLO-[3.1.0]-HEXAN-2-ONE
(4R,6R,7R)-6-tert-Butyldiphenylsilyloxy-7,8-cyclohexylidenedioxyoctan-4-yl 5'-hexenoate
(1R,4S,5S)-6-(TERT.BUTOXYCARBONYL)-4-[(TERT.-BUTYLDIPHENYLSILYLOXY)-METHYL]-3-OXA-6-AZA-BICYCLO-[3.1.0]-HEXAN-2-ONE
(3AR,4R,5R,6AS)-4-ALLYL-5-[[TERT.-BUTYL-(DIPHENYL)-SILYL]-OXY]-4,5,6,6A-TETRAHYDROPENTALEN-1(3AH)-ONE
3,4-BIS-O-TERT.-BUTYL-DIPHENYLSILYL-6-O-FORMYL-D-GLUCAL
(2S,4S,5S,7E,9E,11E)-4-((tert-Butyldiphenylsilyl)oxy)-1,2-(isopropylidenedioxy)-5,7,11-trimethyl-12-(2'-methyloxazol-4'-yl)-7,9,11-dodecatrien-6-one
| Title | Journal or Book | Year |
|---|---|---|
| Enantiospecific Synthesis of a Protected Equivalent of APTO, the β-Amino Acid Fragment of Microsclerodermins C and D, by Aziridino-γ-lactone Methodology | European Journal of Organic Chemistry | 2009 |