1-BETA-[5-(PINACOLATOBORYL)-FURAN-2-YL]-1,2-DIDEOXY-3,5-DI-O-TOLUOYL-D-RIBOFURANOSIDE
Compound with spectra: 1 NMR
![1-BETA-[5-(PINACOLATOBORYL)-FURAN-2-YL]-1,2-DIDEOXY-3,5-DI-O-TOLUOYL-D-RIBOFURANOSIDE](/api/compound/JUNpUTaH60C.png?ph=true&h=300&w=458 "1-BETA-[5-(PINACOLATOBORYL)-FURAN-2-YL]-1,2-DIDEOXY-3,5-DI-O-TOLUOYL-D-RIBOFURANOSIDE")
| SpectraBase Compound ID | JUNpUTaH60C |
|---|---|
| InChI | InChI=1S/C31H35BO8/c1-19-7-11-21(12-8-19)28(33)35-18-26-25(38-29(34)22-13-9-20(2)10-14-22)17-24(36-26)23-15-16-27(37-23)32-39-30(3,4)31(5,6)40-32/h7-16,24-26H,17-18H2,1-6H3/t24-,25+,26-/m0/s1 |
| InChIKey | NMZNGESJJMHOKC-NXCFDTQHSA-N |
| Mol Weight | 546.4 g/mol |
| Molecular Formula | C31H35BO8 |
| Exact Mass | 546.242498 g/mol |
| Enantiomer InChIKey | NMZNGESJJMHOKC-UODIDJSMSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | ACETONE-D6 |
1-BETA-[5-(THIOPHEN-2-YL)-FURAN-2-YL]-1,2-DIDEOXY-3,5-DI-O-TOLUOYL-D-RIBOFURANOSIDE
1-BETA-[5-(PYRIDIN-2-YL)-FURAN-2-YL]-1,2-DIDEOXY-3,5-DI-O-TOLUOYL-D-RIBOFURANOSIDE
1-BETA-[5-(THIAZOL-2-YL)-FURAN-2-YL]-1,2-DIDEOXY-3,5-DI-O-TOLUOYL-D-RIBOFURANOSIDE
1,2-DIDEOXY-1-BETA-[3-(2-NAPHTHYL)-PHENYL]-3,5-DI-O-(4-TOLUOYL)-D-RIBOFURANOSIDE
7-AMINO-2-[2'-DEOXY-3',5'-DI-O-(PARA-TOLUOYL)-ALPHA-D-ERYTHRO-PENTOFURANOSYL]-2H-1,2,3-TRIAZOLO-[4,5-D]-PYRIMIDINE
7-AMINO-2-[2'-DEOXY-3',5'-DI-O-(PARA-TOLUOYL)-BETA-D-ERYTHRO-PENTOFURANOSYL]-2H-1,2,3-TRIAZOLO-[4,5-D]-PYRIMIDINE
(2R,3S)-1,3-BIS-O-(4-METHYLBENZOYL)-5,5-BIS-[5-[(2,4-OXO-5-IMIDAZOLIDINYLIDENE)-METHYL]-FURAN-2-YL]-PENTANE-1,2,3-TRIOL
(3S)-3-HYDROXY-(6R)-6-(2,3,5-TRI-O-BENZOYL-BETA-D-RIBOFURANOSYL)-2,3-DIHYDRO-6H-PYRAN
2-[2'-DEOXY-3',5'-BIS-O-(4-METHYLBENZOYL)-BETA-D-ERYTHRO-PENTOFURANOSYL]-2H-INDAZOLE
OCTYL-2,3,4,6-TETRA-O-BENZOYL-BETA-D-GLUCOPYRANOSIDE
| Title | Journal or Book | Year |
|---|---|---|
| Modular Synthesis of 5-Substituted Furan-2-yl C-2′-Deoxyribonucleosides and Biaryl Covalent Base-Pair Analogues | European Journal of Organic Chemistry | 2010 |