RAC-(4S,5S,6R)-6-[3-[(TERT.-BUTYLDIPHENYLSILYL)-OXY]-PROPYL]-4-[DIMETHYL-(PHENYL)-SILYL]-6-HYDROXY-2-OXASPIRO-[4.4]-NONAN-1-ONE
Compound with spectra: 1 NMR
![RAC-(4S,5S,6R)-6-[3-[(TERT.-BUTYLDIPHENYLSILYL)-OXY]-PROPYL]-4-[DIMETHYL-(PHENYL)-SILYL]-6-HYDROXY-2-OXASPIRO-[4.4]-NONAN-1-ONE](/api/compound/3dhfzifbuNq.png?ph=true&h=300&w=458 "RAC-(4S,5S,6R)-6-[3-[(TERT.-BUTYLDIPHENYLSILYL)-OXY]-PROPYL]-4-[DIMETHYL-(PHENYL)-SILYL]-6-HYDROXY-2-OXASPIRO-[4.4]-NONAN-1-ONE")
| SpectraBase Compound ID | 3dhfzifbuNq |
|---|---|
| InChI | InChI=1S/C35H46O4Si2/c1-33(2,3)41(29-19-11-7-12-20-29,30-21-13-8-14-22-30)39-26-16-24-34(37)23-15-25-35(34)31(27-38-32(35)36)40(4,5)28-17-9-6-10-18-28/h6-14,17-22,31,37H,15-16,23-27H2,1-5H3/t31-,34-,35-/m1/s1 |
| InChIKey | YBMWLQOHZPCYEG-QSADDTNJSA-N |
| Mol Weight | 586.9 g/mol |
| Molecular Formula | C35H46O4Si2 |
| Exact Mass | 586.293463 g/mol |
| Enantiomer InChIKey | YBMWLQOHZPCYEG-NNUTVPELSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
5'-O-(TERT.-BUTYLDIPHENYLSILYL)-3'-DEOXY-2'-O-(2-METHOXYETHYL)-3'-C-(2-PHENYLETHENYL)-5-METHYLURIDINE
2-CHLORO-9-[2-DEOXY-5-O-[(1,1-DIMETHYLETHYL)-DIPHENYLSILYL]-3-O-(PHENOXYTHIOCARBONYL)-BETA-D-ERYTHRO-PENTOFURANOSYL]-9H-PURIN-6-AMINE
OQSFSZYCMWRJSY-SCARYJQKSA-N
(6aRS,8SR,10aSR,10bRS)-3,4,7,8-Tetrahydro-2H-8,10a-epoxy[1,3]oxazino[2,3-a]isoindol-6(6aH,10bH)-one
Methyl 4-Bromo-2-oxotetracyclo[7.4.0.1(3,5).0(6.8)]dodecatriene-7-carboxylate
3-[2-(2-t-Butyldiphenylsilyloxyethyl)-4,5-dimethoxyphenyl]-6,7-dimethoxy-2-methyl-3,4-dihydroisoquinolinium iodomethylate
2-Benzyl-5-nitro-1-tosyl-1,2-dihydro-3H-indazol-3-one
1-ALPHA-HYDROXY-1-DESOXO-ARGLANINE
RAC-N(6),N(6)-DIBENZOYL-3'-([(TERT.-BUTYL)-DIPHENYLSILYLOXY]-METHYL)-2',3',5'-TRIDEOXY-5'-(METHOXYCARBONYL)-1'-A-CARBAADENOSINE;METHYL-T-2-([(TER
N-o-Methylphenyl-trans,trans-.alpha.-carboxyl-.beta.-methoxycarbonyl-.gamma.-p-cholorophenyl-.gamma.-butyrolactam
| Title | Journal or Book | Year |
|---|---|---|
| Development of an additive-controlled, SmI2-mediated stereoselective sequence: Telescoped spirocyclisation, lactone reduction and Peterson elimination | Beilstein Journal of Organic Chemistry | 2013 |