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[(1R)-2-BENZOYL-OXIMO-ENDO-3-BORNYL]-[METHYLENE-(PENTANOIC-ACID-GAMMA-LACTONE-5-YL)]-SELENIDE;MAJOR-ISOMER

Compound with spectra: 2 NMR

[(1R)-2-BENZOYL-OXIMO-ENDO-3-BORNYL]-[METHYLENE-(PENTANOIC-ACID-GAMMA-LACTONE-5-YL)]-SELENIDE;MAJOR-ISOMER
SpectraBase Compound ID CDExJa0fOKs
InChI InChI=1S/C22H27NO4Se/c1-21(2)16-11-12-22(21,3)19(18(16)28-13-15-9-10-17(24)26-15)23-27-20(25)14-7-5-4-6-8-14/h4-8,15-16,18H,9-13H2,1-3H3/b23-19+/t15?,16-,18-,22-/m1/s1
InChIKey LULBEPQYDUHKJO-KGCWGGBASA-N
Mol Weight 448.43 g/mol
Molecular Formula C22H27NO4Se
Exact Mass 449.11053 g/mol
Enantiomer InChIKey LULBEPQYDUHKJO-OZTQDFQUSA-N

View Spectrum of [(1R)-2-BENZOYL-OXIMO-ENDO-3-BORNYL]-[METHYLENE-(PENTANOIC-ACID-GAMMA-LACTONE-5-YL)]-SELENIDE;MAJOR-ISOMER

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of [(1R)-2-BENZOYL-OXIMO-ENDO-3-BORNYL]-[METHYLENE-(PENTANOIC-ACID-GAMMA-LACTONE-5-YL)]-SELENIDE;MAJOR-ISOMER

13C NMR Spectrum
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-(PENTANOIC-ACID-GAMMA-LACTONE-5-YL)]-SELENIDE;MINOR-ISOMER
2-[(2-Benzoyloxyimino-3-selenobornyl)methyl]-3,4-dihydrofuran-5-one
[(1R)-2-BENZOYL-OXIMO-ENDO-3-BORNYL]-TETRAHYDROFURFURYL-SELENIDE;MAJOR-ISOMER
2-(2-Benzoyloximo-3-selenobornyl)methyltetrahydrofuran
[(1R)-2-BENZOYL-OXIMO-ENDO-3-BORNYL]-[METHYLENE-(2-TETRAHYDROPYRANYL)]-SELENIDE;MAJOR-ISOMER
2-(2-Benzoyloximo-3-selenobornyl)methyltetrahydropyran
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
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
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