(3'S,5'S,1''S)-2-[5-[1-(BENZYLOXYCARBONYLAMINO)-2-METHYLPROPYL]-2-OXOTETRAHYDRO-3-FURANYL]-ACETONITRILE
Compound with spectra: 1 NMR
![(3'S,5'S,1''S)-2-[5-[1-(BENZYLOXYCARBONYLAMINO)-2-METHYLPROPYL]-2-OXOTETRAHYDRO-3-FURANYL]-ACETONITRILE](/api/compound/6EvZquFSuuQ.png?ph=true&h=300&w=458 "(3'S,5'S,1''S)-2-[5-[1-(BENZYLOXYCARBONYLAMINO)-2-METHYLPROPYL]-2-OXOTETRAHYDRO-3-FURANYL]-ACETONITRILE")
| SpectraBase Compound ID | 6EvZquFSuuQ |
|---|---|
| InChI | InChI=1S/C18H22N2O4/c1-12(2)16(15-10-14(8-9-19)17(21)24-15)20-18(22)23-11-13-6-4-3-5-7-13/h3-7,12,14-16H,8,10-11H2,1-2H3,(H,20,22)/t14-,15-,16+/m0/s1 |
| InChIKey | KPVILEGGDCSAEM-HRCADAONSA-N |
| Mol Weight | 330.38 g/mol |
| Molecular Formula | C18H22N2O4 |
| Exact Mass | 330.157957 g/mol |
| Enantiomer InChIKey | KPVILEGGDCSAEM-OAGGEKHMSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(3S,5S,1'S)-5-[1-(Benzyloxycarbonylamino)-2-methylpropyl]-3-prop-2-enyl-4,5-dihydro-2(3H)-furanone
(phenylmethyl) N-[(1S)-2-methyl-1-[(2S,4R)-5-oxidanylidene-4-prop-2-enyl-oxolan-2-yl]propyl]carbamate
(R,R)-5-Benzyloxycarbonylamino-6-methylhept-1-en-4-cyclohexyl sulfonate
(2S,3S,5S)-1-Phenyl-2-[(tert-butoxycarbonyl)amino]-3-benzyloxy-5-hydroxy-butadecanone
(2S,3S,5R)-1-Phenyl-2-[(tert-butoxycarbonyl)amino]-3-benzyloxy-5-hydroxy-butadecanone
Carbobenzoxy-L-phenylalanyl-N-benzoyl-L-phenylalaninol
(R,R)-5-Benzyloxycarbonylamino-2-methylhept-1-en-4-cyclohexyl sulfonate
(3S,4S)-1-Phenyl-2-[(tert-butoxycarbonyl)amino]-3-benzyloxy-5-butadecanone
N-CARBOXYBENZYL-4-EXOMETHYLENE-L-PROLINE_ETHYLESTER;MIXTURE_OF_ISOMERS
(1S,6R)-6-Benzyloxycarbonylamino-3,4-dimethylcyclohex-3-ene-1-carboxylic acid
| Title | Journal or Book | Year |
|---|---|---|
| 1,4-Additions to γ-Aminoalkyl-Substituted α-Methylene γ-Butyrolactones: Synthesis of Highly Functionalized Amino Acid Derivatives | Organic Letters | 1999 |