TRANS-(3S,4S)-3-[(METHOXYCARBONYL)-AMINO]-4-ETHYL-2-AZETIDINONE
Compound with spectra: 1 NMR
![TRANS-(3S,4S)-3-[(METHOXYCARBONYL)-AMINO]-4-ETHYL-2-AZETIDINONE](/api/compound/CixFWwoy8iF.png?ph=true&h=300&w=458 "TRANS-(3S,4S)-3-[(METHOXYCARBONYL)-AMINO]-4-ETHYL-2-AZETIDINONE")
| SpectraBase Compound ID | CixFWwoy8iF |
|---|---|
| InChI | InChI=1S/C7H12N2O3/c1-3-4-5(6(10)8-4)9-7(11)12-2/h4-5H,3H2,1-2H3,(H,8,10)(H,9,11)/t4-,5-/m0/s1 |
| InChIKey | TWRBMGLPGOSZEA-WHFBIAKZSA-N |
| Mol Weight | 172.18 g/mol |
| Molecular Formula | C7H12N2O3 |
| Exact Mass | 172.084792 g/mol |
| Enantiomer InChIKey | TWRBMGLPGOSZEA-RFZPGFLSSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | ACETONE-D6 |
N-(2-keto-4-methyl-azetidin-3-yl)carbamic acid tert-butyl ester
1-Propanol, (2S)-2-[(tert.butyloxycarbonyl-(s)-alanyl)amino]-
L-6-amino-2-(carboxyamino)hexanamide, N-tert-butyl ester, oxalate(1.1)
L-4-(carboxyamino)glutaramic acid, N-tert-butyl ester
(S)-N-ALPHA-TERT.-BUTOXYCARBONYLGLUTAMINEAMIDE
2(S)-[(BUTYLOXYCARBONYL)-AMINO]-4-HYDROXY-N,N-DIMETHYLBUTYRAMIDE
12-(N(ALPHA)-TERT.-BUTOXYCARBONYL-L-ALANINOYLAMINO)-DODECANOIC-ACID
(phenylmethyl) N-[(2S)-1-oxidanylidene-1-(propylamino)propan-2-yl]carbamate
N(2)-(Benzyloxycarbonyl)-N(1)-isopropylalaninamide
| Title | Journal or Book | Year |
|---|---|---|
| Enantioselective synthesis of 3-amino-2-azetidinones via the ester enolate - imine condensation | The Journal of Organic Chemistry | 1992 |