(3''S,5''S,1'''S)-DIMETHYL-2-[[5-(1-BENZYLOXYCARBONYLAMINO)-2-METHYLPROPYL]-2-OXOTETRAHYDRO-3-FURANYL]-METHYLMALONATE
Compound with spectra: 1 NMR
![(3''S,5''S,1'''S)-DIMETHYL-2-[[5-(1-BENZYLOXYCARBONYLAMINO)-2-METHYLPROPYL]-2-OXOTETRAHYDRO-3-FURANYL]-METHYLMALONATE](/api/compound/G7HEFmKXWRl.png?ph=true&h=300&w=458 "(3''S,5''S,1'''S)-DIMETHYL-2-[[5-(1-BENZYLOXYCARBONYLAMINO)-2-METHYLPROPYL]-2-OXOTETRAHYDRO-3-FURANYL]-METHYLMALONATE")
| SpectraBase Compound ID | G7HEFmKXWRl |
|---|---|
| InChI | InChI=1S/C22H29NO8/c1-13(2)18(23-22(27)30-12-14-8-6-5-7-9-14)17-11-15(19(24)31-17)10-16(20(25)28-3)21(26)29-4/h5-9,13,15-18H,10-12H2,1-4H3,(H,23,27)/t15-,17-,18+/m0/s1 |
| InChIKey | ABXQIYWNDUAWNC-RYQLBKOJSA-N |
| Mol Weight | 435.47 g/mol |
| Molecular Formula | C22H29NO8 |
| Exact Mass | 435.189317 g/mol |
| Enantiomer InChIKey | ABXQIYWNDUAWNC-NXHRZFHOSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
N-[1-[(2S,4S)-5-keto-4-[(E)-styryl]tetrahydrofuran-2-yl]-2-phenyl-ethyl]carbamic acid tert-butyl ester
(3R)-(2(E)-Phenylethenyl)-5(S)-(1-((tert-butoxycarbonyl)amino)-2-phenethyl)tetrahydrofuran-2-one
erythro-2-Hexulopyranoside, methyl 1,4,5-trideoxy-4-[[(phenylmethoxy)carbonyl]amino]-, 3-acetate
trans-2-methyl-2-methoxy-3-acetoxy-4-benzoxycarbonyl-amino-1-oxa-cyclohexane
(6R,7S,8S,9S)-9-[[(benzyloxy)-carbonyl]amino]-7,8-bis[(methoxymethyl)oxy]tridec-1-en-6-ol
(1R,2S,5R)-5-Methyl-2-(1-methylethyl)cyclohexyl trans-2-(Benzoyloxy)cycloheptylcarbamate
1.beta.-(Mesyloxy)-2.alpha.,3.alpha.-epoxy-4.beta-[(benzyloxycarbonyl)amino]cyclooctane
(5-oxo-4-oxa-5-homoadamantane-2-yl)oxymethylchloride
BEUANPRXZZNUOH-OFAXGOBFSA-N
| 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 |