(3R,5S,1'S)-5-[1-(BENZYLOXYCARBONYLAMINO)-3-METHYLBUTYL]-3-METHOXYMETHYLTETRAHYDROFURAN-2-ONE
Compound with spectra: 1 NMR
![(3R,5S,1'S)-5-[1-(BENZYLOXYCARBONYLAMINO)-3-METHYLBUTYL]-3-METHOXYMETHYLTETRAHYDROFURAN-2-ONE](/api/compound/1jHAES10Ei5.png?ph=true&h=300&w=458 "(3R,5S,1'S)-5-[1-(BENZYLOXYCARBONYLAMINO)-3-METHYLBUTYL]-3-METHOXYMETHYLTETRAHYDROFURAN-2-ONE")
| SpectraBase Compound ID | 1jHAES10Ei5 |
|---|---|
| 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+/m1/s1 |
| InChIKey | VZCTZCNHFOWCCH-ZACQAIPSSA-N |
| Mol Weight | 349.43 g/mol |
| Molecular Formula | C19H27NO5 |
| Exact Mass | 349.188923 g/mol |
| Enantiomer InChIKey | VZCTZCNHFOWCCH-YESZJQIVSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(3R,5S,1'S)-5-[1-(BENZYLOXYCARBONYLAMINO)-2-METHYLPROPYL]-3-PENTYLTETRAHYDROFURAN-2-ONE
(3S,5S,1'S)-5-[1-(BENZYLOXYCARBONYLAMINO)-2-METHYLPROPYL]-3-PENTYLTETRAHYDROFURAN-2-ONE
(phenylmethyl) N-[(1S)-1-[(2S,4S)-4-(2,2-dimethylpropyl)-5-oxidanylidene-oxolan-2-yl]-2-methyl-propyl]carbamate
(3S,5S,1'S)-5-[1-(Benzyloxycarbonylamino)-2-methylpropyl]-3-prop-2-enyl-4,5-dihydro-2(3H)-furanone
(3'S,5'S,1''S)-2-[5-[1-(BENZYLOXYCARBONYLAMINO)-2-METHYLPROPYL]-2-OXOTETRAHYDRO-3-FURANYL]-ACETONITRILE
(2R,1'S,2'S)-2-(2'-CARBOXYBENZYLAMINO-CYCLOHEXYL)-OXY-3-PHENYL-PROPIONIC-ACID;Z-COP-OH
(1R*,5R*,8R*)-8-(TERT.-BUTOXYCARBONYLAMINO)-6-OXABICYCLO-[3.2.1]-OCTAN-7-ONE
(2S,3S,5R)-1-Phenyl-2-[(tert-butoxycarbonyl)amino]-3-benzyloxy-5-hydroxy-butadecanone
(2S,3S,5S)-1-Phenyl-2-[(tert-butoxycarbonyl)amino]-3-benzyloxy-5-hydroxy-butadecanone
| 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 |