#20;(+/-)-(1RS,2RS,3SR,4SR,5SR)-5-EXO-BENZYLAMINO-7-TERT.-BUTOXYCARBONYL-2,3-EXO-ISOPROPYLIDENEDIOXY-7-AZABICYCLO-[2.2.1]-HEPTANE;TERT.-BUTYL-(3ASR,4SR,5SR,7RS
Compound with spectra: 1 NMR
![#20;(+/-)-(1RS,2RS,3SR,4SR,5SR)-5-EXO-BENZYLAMINO-7-TERT.-BUTOXYCARBONYL-2,3-EXO-ISOPROPYLIDENEDIOXY-7-AZABICYCLO-[2.2.1]-HEPTANE;TERT.-BUTYL-(3ASR,4SR,5SR,7RS](/api/compound/Gh4lkxPnLjC.png?ph=true&h=300&w=458 "#20;(+/-)-(1RS,2RS,3SR,4SR,5SR)-5-EXO-BENZYLAMINO-7-TERT.-BUTOXYCARBONYL-2,3-EXO-ISOPROPYLIDENEDIOXY-7-AZABICYCLO-[2.2.1]-HEPTANE;TERT.-BUTYL-(3ASR,4SR,5SR,7RS")
| SpectraBase Compound ID | Gh4lkxPnLjC |
|---|---|
| InChI | InChI=1S/2C21H30N2O4/c2*1-20(2,3)27-19(24)23-15-11-14(22-12-13-9-7-6-8-10-13)16(23)18-17(15)25-21(4,5)26-18/h2*6-10,14-18,22H,11-12H2,1-5H3/t2*14-,15-,16+,17+,18-/m00/s1 |
| InChIKey | DKYYKLMGTSHOPA-YYAAMYSBSA-N |
| Mol Weight | 748.96 g/mol |
| Molecular Formula | C42H60N4O8 |
| Exact Mass | 748.441115 g/mol |
| Enantiomer InChIKey | DKYYKLMGTSHOPA-DADMQYGUSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
#21;(+/-)-(1RS,2RS,3SR,4SR,5RS)-5-ENDO-BENZYLAMINO-7-TERT.-BUTOXYCARBONYL-2,3-EXO-ISOPROPYLIDENEDIOXY-7-AZABICYCLO-[2.2.1]-HEPTANE;TERT.-BUTYL-(3ASR,4SR
N,N-Diethyl-3,7-anhydro-2-[(tert-butoxycarbonyl)1mino]-2-deoxy-4,5;6,8-di-O-isopropylidene-D-erythro-L-gluco-octanamide
2-tert-Butyloxycarbonyl-6-exo,7-exo-isopropylidenedioxy-2-azabicyclo[3.2.1]octan-3-one
1-[(Benzyloxy)carbonyl]-3-(1'-isopropenyl)-8,8-dimethyl-7,9-dioxa-1-aztricycloundecane
[W-(CPH)-[HYDRIDOTRIS-(3,5-DIMETHYLPYRAZOLYL)-BORATE]-BR(2)]
Spermidine fragment C28
1-[5-(4-fluorophenyl)-2-furyl]-2-(4-methoxy-6-methyl-5,6,7,8-tetrahydro[1,3]dioxolo[4,5-g]isoquinolin-5-yl)ethanone
1-Benzylamino-6-methyl-9-carbomethoxymethyl-1,2,3,4-tetrahydrocarbazole
HIRSUTENOL_E
CBZ-L-THR-D-VAL-L-VAL-D-ALLO-THR(PSI-PRO)-D-ASN(TRT)-D-ALA-OH
| 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 |