(3S,4S,5S)-3-[N-(TERT.-BUTOXYCARBONYL)-AMINO]-5-HYDROXYHEXANO-4-LACTONE
Compound with spectra: 1 NMR
![(3S,4S,5S)-3-[N-(TERT.-BUTOXYCARBONYL)-AMINO]-5-HYDROXYHEXANO-4-LACTONE](/api/compound/AJYX1gJ45Rx.png?ph=true&h=300&w=458 "(3S,4S,5S)-3-[N-(TERT.-BUTOXYCARBONYL)-AMINO]-5-HYDROXYHEXANO-4-LACTONE")
| SpectraBase Compound ID | AJYX1gJ45Rx |
|---|---|
| InChI | InChI=1S/C11H19NO5/c1-6(13)9-7(5-8(14)16-9)12-10(15)17-11(2,3)4/h6-7,9,13H,5H2,1-4H3,(H,12,15)/t6-,7?,9+/m1/s1 |
| InChIKey | UQXYPKOMLXDGIV-YUTBPMSOSA-N |
| Mol Weight | 245.27 g/mol |
| Molecular Formula | C11H19NO5 |
| Exact Mass | 245.126323 g/mol |
| Enantiomer InChIKey | UQXYPKOMLXDGIV-JFOAVASISA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
3-[(1-tert-Butoxycarbonylamido)-3-methylbutyl]-2-(methoxymethoxymethyl)oxirane
METHYL-4-(N-TERT.-BUTOXYCARBONYL)-2,3-DIDEOXY-D-THREO-HEXOPYRANOSIDE
N-Boc-2-(phenoxy)cyclohexylamine
3-[1-(tert-Butoxycarbonylamido)-2-methylpropyl]-2-(methoxymethoxymethyloxirane
(3R)-3-(tert-butoxycarbonylamino)-4-(3-ketocyclohexen-1-yl)butyric acid methyl ester
Benzyl (1R,2S)-N-(2-acetoxycyclohexyl)carbamate
Benzyl (1R,2R)-N-(2-acetoxycyclohexyl)carbamate
Benzyl 3-{[(t-butoxy)carbonyl]amino}-2,5-dimethylhexanoate
Benzyl (2S,3S)-3-(t-butoxy)carbonyl]amino-2,5-dimethylhexanoate
| Title | Journal or Book | Year |
|---|---|---|
| Syntheses of derivatives of L-daunosamine and its C-3 epimer employing as the key step the asymmetric conjugate addition of a homochiral lithium amide to tert-butyl (E,E )-hexa-2,4-dienoate | Journal of the Chemical Society, Perkin Transactions 1 | 1999 |