TERT.-BUTYL_(1S,2R,2ïS)-2-[2ï-(N-TERT.-BUTOXYCARBAMOYLMETHYL)-3ï-PHENYLPROPIONYAMINO]-CYCLOHEXANE-1-CARBOXYLATE
Compound with spectra: 1 NMR
![TERT.-BUTYL_(1S,2R,2ïS)-2-[2ï-(N-TERT.-BUTOXYCARBAMOYLMETHYL)-3ï-PHENYLPROPIONYAMINO]-CYCLOHEXANE-1-CARBOXYLATE](/api/compound/8J4h3LIWSwF.png?ph=true&h=300&w=458 "TERT.-BUTYL_(1S,2R,2ïS)-2-[2ï-(N-TERT.-BUTOXYCARBAMOYLMETHYL)-3ï-PHENYLPROPIONYAMINO]-CYCLOHEXANE-1-CARBOXYLATE")
| SpectraBase Compound ID | 8J4h3LIWSwF |
|---|---|
| InChI | InChI=1S/C26H40N2O5/c1-25(2,3)32-24(31)20-14-10-11-15-21(20)27-23(30)19(16-18-12-8-7-9-13-18)17-22(29)28-33-26(4,5)6/h7-9,12-13,19-21H,10-11,14-17H2,1-6H3,(H,27,30)(H,28,29)/t19-,20-,21+/m0/s1 |
| InChIKey | CNXUYAGPDNOVNZ-PCCBWWKXSA-N |
| Mol Weight | 460.6 g/mol |
| Molecular Formula | C26H40N2O5 |
| Exact Mass | 460.293722 g/mol |
| Enantiomer InChIKey | CNXUYAGPDNOVNZ-NJYVYQBISA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
3-METHYL-2-PHENYL-TRANS-DECAHYDROQUINOLIN-4-ONE
7-Benzyl-2-endo-carbethoxy-7-azabicyclo[2.2.1]heptane
Ethyl trans-7-cyano-cis-2-azabicyclo[4.2.0]octane-6-carboxylate
(4R)-3-[(2S)-1-oxo-3-phenyl-2-(phenylmethoxymethyl)propyl]-4-propan-2-yl-2-oxazolidinone
(4R)-3-[(2S)-2-Acetoxymethyl-3-phenylpropanoyl]-4-isopropyloxazolidin-2-one
3-(Phenylmethyl)-1-[3-(trifluoromethyl)phenyl]pyrrolidine-2,5-dione
(1S*,2R*,3S*,4S*,5R*)-3-ACETYLAMINO-5-HYDROXYBICYCLO-[2.2.1]-HEPTANE-2-CARBOXYLIC-ACID
Ethylecgonine
5-Isopropylpxycarbonyl-2-methyl-4-oxo-6-phenyl-5,6-dihydropyrimidine
Ethyl N-[(2-methyl-3-Benzyloxymethyl)-5-hydroxycyclopentyl)methyl]-5-methyl-piperidineacetate
| Title | Journal or Book | Year |
|---|---|---|
| First asymmetric synthesis of the Kelatorphan-like enkephalinase inhibitor (1S,2R,2′S )-2-[2′-(N-hydroxycarbamoylmethyl)-3′-phenylpropionylamino]cyclohexane-1-carboxylic acid | Journal of the Chemical Society, Perkin Transactions 1 | 1998 |