HYDROXYINDOLIZIDINONE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | JrD4wJBIue3 |
|---|---|
| InChI | InChI=1S/C8H11NO2/c10-7-2-1-5-9-6(7)3-4-8(9)11/h1-2,6-7,10H,3-5H2/t6-,7-/m0/s1 |
| InChIKey | UBKCRQGYLOQTGQ-BQBZGAKWSA-N |
| Mol Weight | 153.18 g/mol |
| Molecular Formula | C8H11NO2 |
| Exact Mass | 153.078979 g/mol |
| Enantiomer InChIKey | UBKCRQGYLOQTGQ-RNFRBKRXSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
8-METHYLENE-1,5,8,8A-TETRAHYDRO-2H-INDOLIZIN-3-ONE
(8R,8aS)-8-hydroxy-2,3,6,7,8,8a-hexahydro-1H-indolizin-5-one
1-(2-Propenyl)-5-carbethoxy-2-pyrrolidinone
1-(2-Methyl-2-propenyl)-5-hydroxymethyl-2-pyrrolidinone methanesulfonate
(1R,8aS)-1-Hydroxyhexahydroindolizin-3-one
5-keto-3,6,7,8-tetrahydropyrrolizine-1-carbaldehyde
5-(1-METHYLENE-ALLYL)-1-PENT-4-ENYL-PYRROLIDIN-2-ONE
1-HEX-5-ENYL-5-(1-METHYLENE-ALLYL)-PYRROLIDIN-2-ONE
5-Bromo-1,5,6,8a-tetrahydro-3(2H)-indolizinone
| Title | Journal or Book | Year |
|---|---|---|
| An Oxidative Mannich Cyclization Methodology for the Stereocontrolled Synthesis of Highly Functionalized Piperidines | The Journal of Organic Chemistry | 1998 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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