(2E,2'E)-DIETHYL-4,4'-[2-(TERT.-BUTOXYCARBONYLAMINO)-2-[[(E)-4-ETHOXY-4-OXO-BUT-2-EN-YL-OXY]-METHYL]-PROPANE-1,3-DIYL]-BIS-(OXY)-DIBUT-2-ENOATE
Compound with spectra: 1 NMR
![(2E,2'E)-DIETHYL-4,4'-[2-(TERT.-BUTOXYCARBONYLAMINO)-2-[[(E)-4-ETHOXY-4-OXO-BUT-2-EN-YL-OXY]-METHYL]-PROPANE-1,3-DIYL]-BIS-(OXY)-DIBUT-2-ENOATE](/api/compound/9m3X4Bxql5m.png?ph=true&h=300&w=458 "(2E,2'E)-DIETHYL-4,4'-[2-(TERT.-BUTOXYCARBONYLAMINO)-2-[[(E)-4-ETHOXY-4-OXO-BUT-2-EN-YL-OXY]-METHYL]-PROPANE-1,3-DIYL]-BIS-(OXY)-DIBUT-2-ENOATE")
| SpectraBase Compound ID | 9m3X4Bxql5m |
|---|---|
| InChI | InChI=1S/C27H43NO11/c1-7-36-22(29)13-10-16-33-19-27(28-25(32)39-26(4,5)6,20-34-17-11-14-23(30)37-8-2)21-35-18-12-15-24(31)38-9-3/h10-15H,7-9,16-21H2,1-6H3,(H,28,32)/b13-10+,14-11+,15-12+ |
| InChIKey | MMCRLJWWLGPAIG-DZURWXOBSA-N |
| Mol Weight | 557.6 g/mol |
| Molecular Formula | C27H43NO11 |
| Exact Mass | 557.283611 g/mol |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
Diethyl (Boc-amino)malonate
N-TERT.-BUTYLOXYCARBONYL-L-SERINE-TERT.-BUTYLESTER
ETHYL-(S)-(E)-2-TERT.-BUTOXYCARBONYLAMINOPENT-3-ENOATE
N-Boc-1-aminocyclobutane carboxylic acid
Ethyl [1-(N-(t-Butoxycarbonyl)amino)cyclopropyl]-methanol
Acetic acid, cyano[[(1,1-dimethylethoxy)carbonyl]amino]-, 1,1-dimethylethyl ester, (.+-.)-
L-2-oxotetrahydro-3-furancarbamic acid, tert-butyl ester
N-[(3R)-2-ketotetrahydrofuran-3-yl]carbamic acid tert-butyl ester
2-(E)-Hexenoic acid, (4S)-4-[(t-butoxycarbonyl)amino]-5-methyl-, ethyl ester
(3S,5S)-4-tert-Butoxycarbonyl-3,5-dimethylmorpholine
| Title | Journal or Book | Year |
|---|---|---|
| Two-directional synthesis as a tool for diversity-oriented synthesis: Synthesis of alkaloid scaffolds | Beilstein Journal of Organic Chemistry | 2012 |