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

Compound with spectra: 2 NMR

[(1R)-2-OXIMO-ENDO-3-BORNYL]-(2-METHOXY-1-CYCLOPENTYL)-SELENIDE;MAJOR-ISOMER
SpectraBase Compound ID 1eoDVleUW4r
InChI InChI=1S/C16H27NO2Se/c1-15(2)10-8-9-16(15,3)14(17-18)13(10)20-12-7-5-6-11(12)19-4/h10-13,18H,5-9H2,1-4H3/b17-14-/t10-,11?,12?,13-,16-/m1/s1
InChIKey DJIXEKRJQXZRSH-UMOMFGBUSA-N
Mol Weight 344.37 g/mol
Molecular Formula C16H27NO2Se
Exact Mass 345.120701 g/mol
Enantiomer InChIKey DJIXEKRJQXZRSH-LUFWSDRLSA-N

View Spectrum of [(1R)-2-OXIMO-ENDO-3-BORNYL]-(2-METHOXY-1-CYCLOPENTYL)-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-OXIMO-ENDO-3-BORNYL]-(2-METHOXY-1-CYCLOPENTYL)-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-OXIMO-ENDO-3-BORNYL]-(2-METHOXY-1-CYCLOPENTYL)-SELENIDE;MINOR-ISOMER
1-Methoxy-2-(2-oximo-3-benzoyloxyselenobornyl)cyclopentane
[(1R)-2-OXIMO-ENDO-3-BORNYL]-(2-METHOXY-1-CYCLOHEXYL)-SELENIDE;MAJOR-ISOMER
1-Methoxy-2-(2-oximo-3-selenobornyl)cyclohexane
[(1R)-2-OXIMO-ENDO-3-BORNYL]-(6-METHOXY-5-DECANYL)-SELENIDE
[(1R)-2-OXIMO-ENDO-3-BORNYL]-(2-METHOXY-1-CYCLOHEPTYL)-SELENIDE;MAJOR-ISOMER
[(1R)-2-OXIMO-ENDO-3-BORNYL]-[METHYLENE-(2,3-DIHYDRO-BENZOFURAN-2-YL)]-SELENIDE;MAJOR-ISOMER
2-[(2-Oximo-3-selenobornyl)methyl]-2,3-dihydrobenzofuran
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
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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