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[(1R)-2-BENZOYL-OXIMO-ENDO-3-BORNYL]-TETRAHYDROFURFURYL-SELENIDE;MAJOR-ISOMER

Compound with spectra: 2 NMR

[(1R)-2-BENZOYL-OXIMO-ENDO-3-BORNYL]-TETRAHYDROFURFURYL-SELENIDE;MAJOR-ISOMER
SpectraBase Compound ID E6C2FKhwe15
InChI InChI=1S/C22H29NO3Se/c1-21(2)17-11-12-22(21,3)19(18(17)27-14-16-10-7-13-25-16)23-26-20(24)15-8-5-4-6-9-15/h4-6,8-9,16-18H,7,10-14H2,1-3H3/b23-19+/t16?,17-,18-,22-/m1/s1
InChIKey JXSUHMIICDPBFZ-XBKLNURQSA-N
Mol Weight 434.45 g/mol
Molecular Formula C22H29NO3Se
Exact Mass 435.131266 g/mol
Enantiomer InChIKey JXSUHMIICDPBFZ-MCFQZAOUSA-N

View Spectrum of [(1R)-2-BENZOYL-OXIMO-ENDO-3-BORNYL]-TETRAHYDROFURFURYL-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]-TETRAHYDROFURFURYL-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]-TETRAHYDROFURFURYL-SELENIDE;MINOR-ISOMER
2-(2-Benzoyloximo-3-selenobornyl)methyltetrahydrofuran
[(1R)-2-BENZOYL-OXIMO-ENDO-3-BORNYL]-[METHYLENE-(2-TETRAHYDROPYRANYL)]-SELENIDE;MAJOR-ISOMER
2-[(2-Benzoyloxyimino-3-selenobornyl)methyl]-3,4-dihydrofuran-5-one
DI-[(1R)-2-O-BENZOYL-OXIMO-ENDO-3-BORNYL]-DISELENIDE
[(1R)-2-OXIMO-ENDO-3-BORNYL]-(2-METHOXY-1-CYCLOHEPTYL)-SELENIDE;MAJOR-ISOMER
[(1R)-2-OXIMO-ENDO-3-BORNYL]-(6-METHOXY-5-DECANYL)-SELENIDE
1-Methoxy-2-(2-oximo-3-selenobornyl)cyclohexane
[(1R)-2-OXIMO-ENDO-3-BORNYL]-(2-METHOXY-1-CYCLOHEXYL)-SELENIDE;MAJOR-ISOMER
[(1R)-2-OXIMO-ENDO-3-BORNYL]-(2-METHOXY-1-CYCLOPENTYL)-SELENIDE;MAJOR-ISOMER
1-Methoxy-2-(2-oximo-3-benzoyloxyselenobornyl)cyclopentane
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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