#11;(+/-)-(1SR,4RS,5SR,6RS)-7-TERT.-BUTOXYCARBONYL-6-ENDO-PARA-TOLUENESULFONYL-7-AZABICYCLO-[2.2.1]-HEPT-2-EN-5-ENDO-OL;TERT.-BUTYL-(1SR,4RS,5SR,6RS)-5-
Compound with spectra: 1 NMR
![#11;(+/-)-(1SR,4RS,5SR,6RS)-7-TERT.-BUTOXYCARBONYL-6-ENDO-PARA-TOLUENESULFONYL-7-AZABICYCLO-[2.2.1]-HEPT-2-EN-5-ENDO-OL;TERT.-BUTYL-(1SR,4RS,5SR,6RS)-5-](/api/compound/8a9VaS0P4Dv.png?ph=true&h=300&w=458 "#11;(+/-)-(1SR,4RS,5SR,6RS)-7-TERT.-BUTOXYCARBONYL-6-ENDO-PARA-TOLUENESULFONYL-7-AZABICYCLO-[2.2.1]-HEPT-2-EN-5-ENDO-OL;TERT.-BUTYL-(1SR,4RS,5SR,6RS)-5-")
| SpectraBase Compound ID | 8a9VaS0P4Dv |
|---|---|
| InChI | InChI=1S/C18H23NO5S/c1-11-5-7-12(8-6-11)25(22,23)16-14-10-9-13(15(16)20)19(14)17(21)24-18(2,3)4/h5-10,13-16,20H,1-4H3/t13-,14+,15-,16+/m0/s1 |
| InChIKey | HEAIOYWOPVVORW-XUWVNRHRSA-N |
| Mol Weight | 365.44 g/mol |
| Molecular Formula | C18H23NO5S |
| Exact Mass | 365.129694 g/mol |
| Enantiomer InChIKey | HEAIOYWOPVVORW-QXSJWSMHSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | DMSO-D6 |
2-Phenyl-4-(phenylsulfonyl)-1,6-dioxaspiro[4.5]decan-10-one
ISOSTREPTAZOLIN
#-32-(S)-MOSHER-AMIDE;(2'S,2''S)-4-[2'-METHOXYCARBONYL-2'-(3'',3'',3''-TRIFLUORO-2''-METHOXY-2''-PHENYL-PROPIONYLAMINO)-ETHYL]-2,6-DIMETHYL-PYRIDINE-3,5-DICARBOXYLIC
#-32-(R)-MOSHER-AMIDE;(2'S,2''R)-4-[2'-METHOXYCARBONYL-2'-(3'',3'',3''-TRIFLUORO-2''-METHOXY-2''-PHENYL-PROPIONYLAMINO)-ETHYL]-2,6-DIMETHYL-PYRIDINE-3,5-DICARBOXYLIC
2-{[(1-(4-amino-1,2,5-oxadiazol-3-yl)-4-{[(2E)-2-(1,3-benzodioxol-5-ylmethylene)hydrazino]carbonyl}-1H-1,2,3-triazol-5-yl)methyl]amino}benzamide
N-n-Butyl-1-methyl-4-aza-2,6-dioxatetracyclo[3.2.1.1(1,3).1(5,7)]dodecane
6-PARA-HYDROXYBENZYLAROMADENDRIN;GERICUDRANIN-E
ETHYL-1-(4-CHLOROBENZYL)-3-(2,2-DICYANOETHYL)-INDOLE-2-CARBOXYLATE
2-PHENYL-2'-DI-TERT.-BUTYLPHOSPHINO-1,1'-BINAPHTHYL
(17Z)-17-methoxyimino-15,16-dihydrocyclopenta[a]phenanthrene-3,4-dione
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis of Enantiomerically Pure 1,2-Diamine Derivatives of 7-Azabicyclo[2.2.1]heptane. New Leads as Glycosidase Inhibitors and Rigid Scaffolds for the Preparation of Peptide Analogues | The Journal of Organic Chemistry | 2003 |