(3S,5S,1'S)-5-[1-(BENZYLOXYCARBONYLAMINO)-3-METHYLBUTYL]-3-METHOXYMETHYLTETRAHYDROFURAN-2-ONE
Compound with spectra: 1 NMR
![(3S,5S,1'S)-5-[1-(BENZYLOXYCARBONYLAMINO)-3-METHYLBUTYL]-3-METHOXYMETHYLTETRAHYDROFURAN-2-ONE](/api/compound/3P2FVytgf93.png?ph=true&h=300&w=458 "(3S,5S,1'S)-5-[1-(BENZYLOXYCARBONYLAMINO)-3-METHYLBUTYL]-3-METHOXYMETHYLTETRAHYDROFURAN-2-ONE")
| SpectraBase Compound ID | 3P2FVytgf93 |
|---|---|
| InChI | InChI=1S/C19H27NO5/c1-13(2)9-16(17-10-15(12-23-3)18(21)25-17)20-19(22)24-11-14-7-5-4-6-8-14/h4-8,13,15-17H,9-12H2,1-3H3,(H,20,22)/t15-,16+,17-/m0/s1 |
| InChIKey | VZCTZCNHFOWCCH-BBWFWOEESA-N |
| Mol Weight | 349.43 g/mol |
| Molecular Formula | C19H27NO5 |
| Exact Mass | 349.188923 g/mol |
| Enantiomer InChIKey | VZCTZCNHFOWCCH-IXDOHACOSA-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
(3'S,5'S,1''S)-2-[5-[1-(BENZYLOXYCARBONYLAMINO)-2-METHYLPROPYL]-2-OXOTETRAHYDRO-3-FURANYL]-ACETONITRILE
(2S,3S,5R)-1-Phenyl-2-[(tert-butoxycarbonyl)amino]-3-benzyloxy-5-hydroxy-butadecanone
(+)-5-BENZYLOXYCARBONYL-AMINO-5-DEOXY-L-IDOFURANOSE
(3S,4S)-1-Phenyl-2-[(tert-butoxycarbonyl)amino]-3-benzyloxy-5-butadecanone
(R,R)-5-Benzyloxycarbonylamino-2-methylhept-1-en-4-cyclohexyl sulfonate
N-CARBOXYBENZYL-4-EXOMETHYLENE-L-PROLINE_ETHYLESTER;MIXTURE_OF_ISOMERS
TERT.-BUTYL-[(2R)-N-BENZYLOXYCARBONYL-ALPHA-METHYL-ASPARTYL]-BETA-(2S)-PHENYLALANINATE-DIESTER
| 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 |