(2S,8R)-2-[[(TERT.-BUTYLDIMETHYL)-OXY)-METHYL]-8-[[(TERT.-BUTYLDIPHENYLSILYL)-OXY]-METHYL]-1-[(4-METHYLPHENYL)-SULFONYL]-1,5,9-TRIAZABICYCLO-[4.4.0]-DEC-9-ENE
Compound with spectra: 1 NMR
![(2S,8R)-2-[[(TERT.-BUTYLDIMETHYL)-OXY)-METHYL]-8-[[(TERT.-BUTYLDIPHENYLSILYL)-OXY]-METHYL]-1-[(4-METHYLPHENYL)-SULFONYL]-1,5,9-TRIAZABICYCLO-[4.4.0]-DEC-9-ENE](/api/compound/97YXzis2dbI.png?ph=true&h=300&w=458 "(2S,8R)-2-[[(TERT.-BUTYLDIMETHYL)-OXY)-METHYL]-8-[[(TERT.-BUTYLDIPHENYLSILYL)-OXY]-METHYL]-1-[(4-METHYLPHENYL)-SULFONYL]-1,5,9-TRIAZABICYCLO-[4.4.0]-DEC-9-ENE")
| SpectraBase Compound ID | 97YXzis2dbI |
|---|---|
| InChI | InChI=1S/C38H55N3O4SSi2/c1-30-20-22-33(23-21-30)46(42,43)41-32(29-44-47(8,9)37(2,3)4)25-27-40-26-24-31(39-36(40)41)28-45-48(38(5,6)7,34-16-12-10-13-17-34)35-18-14-11-15-19-35/h10-23,31-32H,24-29H2,1-9H3/t31?,32-/m1/s1 |
| InChIKey | ICPKLHAYXNETSW-IADGFXSZSA-N |
| Mol Weight | 706.1 g/mol |
| Molecular Formula | C38H55N3O4SSi2 |
| Exact Mass | 705.345182 g/mol |
| Enantiomer InChIKey | ICPKLHAYXNETSW-JYUUXGOASA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
5'-O-(TERT.-BUTYLDIPHENYLSILYL)-2',3'-DIDEOXY-2'-BETA-FLUORO-3'-C-[(HYDROXYPHOSPHINYL)-METHYL]-5-METHYLURIDINE
METHYL-(METHYL-5-ACETAMIDO-3,5-DIDEOXY-9-O-TERT.-BUTYL-DIPHENYLSILYL-D-GLYCERO-BETA-D-GALACTO-NON-2-ULOPYRANOSID)-ONATE
4-CHLORO-7-[2-DEOXY-5-O-[(1,1-DIMETHYLETHYL]-DIPHENYLSILYL]-3-O-(METHYLSULFONYL)-BETA-D-ERYTHRO-PENTOFURANOSYL]-7H-PYRROLO-[2,3-D]-PYRIMIDINE
5'-O-(TERT.-BUTYLDIPHENYLSILYL)-2',3'-DIDEOXY-2'-BETA-FLUORO-3'-C-(2-PHENYLETHENYL)-5-METHYLURIDINE
(3Z,7R)-1,6-Anhydro-4-O-(tert-butyldiphenylsilyl)-2-O-(1'-ethoxy-2'-iodoethyl)-3-deoxy-3-methoxyimine-.beta.,D-arabino-hexopyranose
5'-O-(TERT.-BUTYLDIPHENYLSILYL)-2'-O-[2-[(N,N-DIMETHYLAMINO)-OXY]-ETHYL]-5-METHYL-URIDINE
N-Methyl-2-oxo-N-(1-phenylethyl)-2-[1-(toluene-4-sulfonyl)-1H-indol-3-yl]acetamide
JWH-018 2-Hydroxyindole metabolite
2,4-DI-O-BENZOYL-3-O-BENZYL-6-O-(TERT.-BUTYLDIPHENYLSILYL)-ALPHA-D-GALACTOPYRANOSYL-TRICHLOROACETIMIDATE
| Title | Journal or Book | Year |
|---|---|---|
| Abiotic anion receptor functions. A facile and dependable access to chiral guanidinium anchor groups | The Journal of Organic Chemistry | 1990 |