[(1R)-2-BENZOYL-OXIMO-ENDO-3-BORNYL]-[METHYLENE-(2-TETRAHYDROPYRANYL)]-SELENIDE;MAJOR-ISOMER
Compound with spectra: 2 NMR
![[(1R)-2-BENZOYL-OXIMO-ENDO-3-BORNYL]-[METHYLENE-(2-TETRAHYDROPYRANYL)]-SELENIDE;MAJOR-ISOMER](/api/compound/7vQ0CNcaGmy.png?ph=true&h=300&w=458 "[(1R)-2-BENZOYL-OXIMO-ENDO-3-BORNYL]-[METHYLENE-(2-TETRAHYDROPYRANYL)]-SELENIDE;MAJOR-ISOMER")
| SpectraBase Compound ID | 7vQ0CNcaGmy |
|---|---|
| InChI | InChI=1S/C23H31NO3Se/c1-22(2)18-12-13-23(22,3)20(19(18)28-15-17-11-7-8-14-26-17)24-27-21(25)16-9-5-4-6-10-16/h4-6,9-10,17-19H,7-8,11-15H2,1-3H3/b24-20+/t17?,18-,19-,23-/m1/s1 |
| InChIKey | RGGBOQFILCZROB-PTOATKBQSA-N |
| Mol Weight | 448.48 g/mol |
| Molecular Formula | C23H31NO3Se |
| Exact Mass | 449.146916 g/mol |
| Enantiomer InChIKey | RGGBOQFILCZROB-CUMJKYCVSA-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]-[METHYLENE-(2-TETRAHYDROPYRANYL)]-SELENIDE;MINOR-ISOMER
[(1R)-2-BENZOYL-OXIMO-ENDO-3-BORNYL]-TETRAHYDROFURFURYL-SELENIDE;MAJOR-ISOMER
2-(2-Benzoyloximo-3-selenobornyl)methyltetrahydrofuran
2-[(2-Benzoyloxyimino-3-selenobornyl)methyl]-3,4-dihydrofuran-5-one
DI-[(1R)-2-O-BENZOYL-OXIMO-ENDO-3-BORNYL]-DISELENIDE
1-Methoxy-2-(2-oximo-3-selenobornyl)cycloheptane
[(1R)-2-OXIMO-ENDO-3-BORNYL]-(2-METHOXY-1-CYCLOHEPTYL)-SELENIDE;MAJOR-ISOMER
[(1R)-2-OXIMO-ENDO-3-BORNYL]-(6-METHOXY-5-DECANYL)-SELENIDE
[(1R)-2-OXIMO-ENDO-3-BORNYL]-(2-METHOXY-1-CYCLOHEXYL)-SELENIDE;MAJOR-ISOMER
1-Methoxy-2-(2-oximo-3-selenobornyl)cyclohexane
| 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 |