[(1R)-2-OXIMO-ENDO-3-BORNYL]-(2-METHOXY-1-CYCLOHEXYL)-SELENIDE;MAJOR-ISOMER
Compound with spectra: 1 NMR
![[(1R)-2-OXIMO-ENDO-3-BORNYL]-(2-METHOXY-1-CYCLOHEXYL)-SELENIDE;MAJOR-ISOMER](/api/compound/61ZcdvVcSpV.png?ph=true&h=300&w=458 "[(1R)-2-OXIMO-ENDO-3-BORNYL]-(2-METHOXY-1-CYCLOHEXYL)-SELENIDE;MAJOR-ISOMER")
| SpectraBase Compound ID | 61ZcdvVcSpV |
|---|---|
| InChI | InChI=1S/C17H29NO2Se/c1-16(2)11-9-10-17(16,3)15(18-19)14(11)21-13-8-6-5-7-12(13)20-4/h11-14,19H,5-10H2,1-4H3/b18-15-/t11-,12?,13?,14-,17-/m1/s1 |
| InChIKey | SMSODDCBUSLUSP-OGVDILPMSA-N |
| Mol Weight | 358.4 g/mol |
| Molecular Formula | C17H29NO2Se |
| Exact Mass | 359.136351 g/mol |
| Enantiomer InChIKey | SMSODDCBUSLUSP-LVJSSSMZSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
[(1R)-2-OXIMO-ENDO-3-BORNYL]-(2-METHOXY-1-CYCLOHEPTYL)-SELENIDE;MAJOR-ISOMER
1-Methoxy-2-(2-oximo-3-benzoyloxyselenobornyl)cyclopentane
[(1R)-2-OXIMO-ENDO-3-BORNYL]-(2-METHOXY-1-CYCLOPENTYL)-SELENIDE;MAJOR-ISOMER
[(1R)-2-OXIMO-ENDO-3-BORNYL]-(6-METHOXY-5-DECANYL)-SELENIDE
[(1R)-2-BENZOYL-OXIMO-ENDO-3-BORNYL]-[METHYLENE-(2-TETRAHYDROPYRANYL)]-SELENIDE;MAJOR-ISOMER
2-(2-Benzoyloximo-3-selenobornyl)methyltetrahydrofuran
[(1R)-2-BENZOYL-OXIMO-ENDO-3-BORNYL]-TETRAHYDROFURFURYL-SELENIDE;MAJOR-ISOMER
DI-[(1R)-2-O-BENZOYL-OXIMO-ENDO-3-BORNYL]-DISELENIDE
1-[(3Z)-3-(hydroxyimino)-4,7,7-trimethylbicyclo[2.2.1]hept-2-yl]pyridinium 4-[(E)-(4-anilinophenyl)diazenyl]benzenesulfonate
| 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 |