ETHYL-[(1RS,2RS,3SR,4RS)-3-ENDO-(BENZYLOXY)-5-OXO-7-OXABICYCLO-[2.2.1]-HEPT-2-EXO-YL]-CARBAMATE
Compound with spectra: 1 NMR
![ETHYL-[(1RS,2RS,3SR,4RS)-3-ENDO-(BENZYLOXY)-5-OXO-7-OXABICYCLO-[2.2.1]-HEPT-2-EXO-YL]-CARBAMATE](/api/compound/508dzA4jXPh.png?ph=true&h=300&w=458 "ETHYL-[(1RS,2RS,3SR,4RS)-3-ENDO-(BENZYLOXY)-5-OXO-7-OXABICYCLO-[2.2.1]-HEPT-2-EXO-YL]-CARBAMATE")
| SpectraBase Compound ID | 508dzA4jXPh |
|---|---|
| InChI | InChI=1S/C16H19NO5/c1-2-20-16(19)17-13-12-8-11(18)14(22-12)15(13)21-9-10-6-4-3-5-7-10/h3-7,12-15H,2,8-9H2,1H3,(H,17,19)/t12-,13-,14+,15+/m1/s1 |
| InChIKey | IQQHHPWRSOVMNA-KBXIAJHMSA-N |
| Mol Weight | 305.33 g/mol |
| Molecular Formula | C16H19NO5 |
| Exact Mass | 305.126323 g/mol |
| Enantiomer InChIKey | IQQHHPWRSOVMNA-BYNSBNAKSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
TERT.-BUTYL-[(1RS,2RS,3SR,4RS)-3-ENDO-(BENZYLOXY)-5-OXO-7-OXABICYCLO-[2.2.1]-HEPT-2-EXO-YL]-CARBAMATE
(1S,4S,5S,6R)-6-endo-Benzyloxy-5-exo-tert-butyldimethylsilyloxy-7-oxa-bicyclo(2.2.1)heptan-2-one
Methyl 2-[N-(Benzoxycarbonyl)amino]-3-O-benzyl-2,6-dideoxy-6-iodo-.alpha.-D-glucopyranoside
METHYL-2-ACETAMIDO-3,6-DI-O-BENZYL-2-DEOXY-BETA-D-TALOPYRANOSIDE
(1-S,5-S,1'-S,2'-S)-1-ACETOXY-5-[2,3-BIS-(BENZYLOXY)-1-TERT.-BUTOXYCARBONYLAMINOPROPYL]-2-CYCLOPENTENE
2,3,5-TRI-O-BENZYL-4-CARBOBENZYLOXYAMINO-4-DEOXY-1-O-TRITYL-D-ARABINITOL
3-ACETAMIDO-2,5,6,7-TETRA-O-BENZYL-3-DEOXY-D-GLYCERO-D-GALACTO-HEPTITOL
3,4,6,7-TETRA-O-BENZYL-2,5-DIDEOXY-2,5-IMINO-D-GLYCERO-D-GLUCO-HEPTONONITRILE
(4-S,1'-R,2'-R,3'-R)-4-(1'-BENZYLAMINO-2',3'-DIBENZYLOXY-4'-HYDROXY-BUT-1'-YL)-2,2-DIMETHYL-1,3-DIOXOLANE
METHYL-4-AZIDO-2,3-DI-O-BENZYL-4-DEOXY-BETA-D-GLUCOPYRANOSIDE
| Title | Journal or Book | Year |
|---|---|---|
| Acid-Catalyzed Rearrangement of 3-Aza-8-oxatricyclo[3.2.1. 02,4]octan-6-one Acetals. Highly Stereoselective Total Synthesis of 3-Amino-3-deoxy-D-altrose and Derivatives | Helvetica Chimica Acta | 1989 |