(5S,6S)-6-[1-(TERT.-BUTYLDIPHENYLSILYLOXY)-4-PHENYL-BUT-3-ENYL]-3-(TRIFLUOROMETHYLSULFONYL)-FURAN-2(5H)-ONE
Compound with spectra: 1 NMR
![(5S,6S)-6-[1-(TERT.-BUTYLDIPHENYLSILYLOXY)-4-PHENYL-BUT-3-ENYL]-3-(TRIFLUOROMETHYLSULFONYL)-FURAN-2(5H)-ONE](/api/compound/4s9fZlFyZ8F.png?ph=true&h=300&w=458 "(5S,6S)-6-[1-(TERT.-BUTYLDIPHENYLSILYLOXY)-4-PHENYL-BUT-3-ENYL]-3-(TRIFLUOROMETHYLSULFONYL)-FURAN-2(5H)-ONE")
| SpectraBase Compound ID | 4s9fZlFyZ8F |
|---|---|
| InChI | InChI=1S/C31H31F3O6SSi/c1-30(2,3)42(24-17-9-5-10-18-24,25-19-11-6-12-20-25)40-26(21-13-16-23-14-7-4-8-15-23)27-22-28(29(35)38-27)39-41(36,37)31(32,33)34/h4-20,22,26-27H,21H2,1-3H3/b16-13+/t26-,27-/m0/s1 |
| InChIKey | YPKWFBJCEJTPMN-AGJAMOJTSA-N |
| Mol Weight | 616.72 g/mol |
| Molecular Formula | C31H31F3O6SSi |
| Exact Mass | 616.156271 g/mol |
| Enantiomer InChIKey | YPKWFBJCEJTPMN-RFCCZICOSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(1R,4S,5S)-4-[(1S)-1-(TERT.-BUTYLDIPHENYLSILYLOXY)-4-PHENYL-BUT-3-ENYL]-3-OXA-6-AZA-BICYCLO-[3.1.0]-HEXAN-2-ONE
(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
3-O-[(1',1'-Dimethylethyl)diphenylsilyl]-D-talonic acid - .gamma.-lactone
(4R,6R,7R)-6-tert-Butyldiphenylsilyloxy-7,8-cyclohexylidenedioxyoctan-4-yl 5'-hexenoate
4,6-Dichloro-2-{[(1',1'-dimethylethyl)diphenylsilyl]oxy}-4-cyclohexene-1,3-diol - 3-acetate
tert-Butyl-[(2R,3R,5R)-5-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]-2-(2-phenylmethoxyethyl)oxolan-3-yl]oxy-diphenyl-silane
(1S,3R,4S,5R)-5-t-Butyldoihenylsilyloxy-3-mesyloxy-4-ethyl-1-(methoxycarbonyl)cyclohexane
1,7-Dioxaspiro[5.5]undecane, 2-buten-1-ol deriv.
(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
1D-1-O-(TERT.-BUTYLDIPHENYLSILYL)-3-(DIMETHYLMETHYLENEPHOSPHONATE)-2,4,5,6-O-TETRAKIS-(METHOXYMETHYLENE)-MYO-INOSITOL
| 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 |