[(1R)-2-BENZOYL-OXIMO-ENDO-3-BORNYL]-(2-METHOXY-1-CYCLOHEXYL)-SELENIDE;MAJOR-ISOMER
Compound with spectra: 2 NMR
![[(1R)-2-BENZOYL-OXIMO-ENDO-3-BORNYL]-(2-METHOXY-1-CYCLOHEXYL)-SELENIDE;MAJOR-ISOMER](/api/compound/4oZ0kbzGZr8.png?ph=true&h=300&w=458 "[(1R)-2-BENZOYL-OXIMO-ENDO-3-BORNYL]-(2-METHOXY-1-CYCLOHEXYL)-SELENIDE;MAJOR-ISOMER")
| SpectraBase Compound ID | 4oZ0kbzGZr8 |
|---|---|
| InChI | InChI=1S/C24H33NO3Se/c1-23(2)17-14-15-24(23,3)21(25-28-22(26)16-10-6-5-7-11-16)20(17)29-19-13-9-8-12-18(19)27-4/h5-7,10-11,17-20H,8-9,12-15H2,1-4H3/b25-21-/t17-,18?,19?,20-,24-/m1/s1 |
| InChIKey | SYUXWHKONGLJKC-SLQFGURWSA-N |
| Mol Weight | 462.5 g/mol |
| Molecular Formula | C24H33NO3Se |
| Exact Mass | 463.162566 g/mol |
| Enantiomer InChIKey | SYUXWHKONGLJKC-XGNNGUNDSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
- [(1R)-2-BENZOYL-OXIMO-ENDO-3-BORNYL]-(2-METHOXY-1-CYCLOHEXYL)-SELENIDE;MINOR-ISOMER
1-Methoxy-2-(2-benzoyloxyoxime-3-selenobornyl)cycloheptane
[(1R)-2-O-BENZOYL-OXIMO-ENDO-3-BORNYL]-(6-METHOXY-5-DECANYL)-SELENIDE
5-Methoxy-6-(2-benzoyloximo-3-selenobornyl)decane
[(1R)-2-BENZOYL-OXIMO-ENDO-3-BORNYL]-(2-METHOXY-1-CYCLOPENTYL)-SELENIDE;MAJOR-ISOMER
cis-1-Methoxy-2-[(2-benzoyloxyoximo-3-bornyl)seleno]cyclopentane
Methyl 5-oxo-3-(thien-2'-yl)-2-(camphorylseleno)hexanoate
2-AMINO-3-PIPERIDINO-1,4-DIFLUOROANTHRAQUINONE
benzoic acid, 2-[[[2,3-dihydro-1,3-dioxo-2-(2,4,6-trimethylphenyl)-1H-isoindol-5-yl]carbonyl]amino]-4,5-dimethoxy-
PALIURINE-E
| Title | Journal or Book | Year |
|---|---|---|
| Asymmetric Methoxyselenenylations and Cyclizations with 3-Camphorseleno Electrophiles Containing Oxime Substituents at C-2. Formation of an Unusual Oxaselenazole from an Oxime-Substituted Selenenyl Bromide | The Journal of Organic Chemistry | 2002 |