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

Compound with spectra: 2 NMR

[(1R)-2-OXIMO-ENDO-3-BORNYL]-(2-METHOXY-1-CYCLOHEPTYL)-SELENIDE;MAJOR-ISOMER
SpectraBase Compound ID CSL1VK7CC4b
InChI InChI=1S/C18H31NO2Se/c1-17(2)12-10-11-18(17,3)16(19-20)15(12)22-14-9-7-5-6-8-13(14)21-4/h12-15,20H,5-11H2,1-4H3/b19-16-/t12-,13?,14?,15-,18-/m1/s1
InChIKey PMZBZAYBOARLIR-XRPMGNNSSA-N
Mol Weight 372.42 g/mol
Molecular Formula C18H31NO2Se
Exact Mass 373.152001 g/mol
Enantiomer InChIKey PMZBZAYBOARLIR-RPCAKVNQSA-N

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