For citations & permissions, please see: Citations & Permissions - Wiley Science Solutions*

*Links on SpectraBase are not permalinks.

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

Compound with spectra: 2 NMR

[(1R)-2-BENZOYL-OXIMO-ENDO-3-BORNYL]-(2-METHOXY-1-CYCLOHEPTYL)-SELENIDE;MAJOR-ISOMER
SpectraBase Compound ID BGBeJsHKGKN
InChI InChI=1S/C25H35NO3Se/c1-24(2)18-15-16-25(24,3)22(26-29-23(27)17-11-7-5-8-12-17)21(18)30-20-14-10-6-9-13-19(20)28-4/h5,7-8,11-12,18-21H,6,9-10,13-16H2,1-4H3/b26-22-/t18-,19?,20?,21-,25-/m1/s1
InChIKey XSHKUCAWOAHTNP-RDHJHJCPSA-N
Mol Weight 476.5 g/mol
Molecular Formula C25H35NO3Se
Exact Mass 477.178216 g/mol
Enantiomer InChIKey XSHKUCAWOAHTNP-PBMRUHOQSA-N

View Spectrum of [(1R)-2-BENZOYL-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-BENZOYL-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-BENZOYL-OXIMO-ENDO-3-BORNYL]-(2-METHOXY-1-CYCLOHEPTYL)-SELENIDE;MINOR-ISOMER
1-Methoxy-2-(2-benzoyloxyoxime-3-selenobornyl)cycloheptane
[(1R)-2-BENZOYL-OXIMO-ENDO-3-BORNYL]-(2-METHOXY-1-CYCLOHEXYL)-SELENIDE;MAJOR-ISOMER
1-Methoxy-2-[(2-benzoyloxyoximo-3-bornylseleno)]cyclohexane
5-Methoxy-6-(2-benzoyloximo-3-selenobornyl)decane
[(1R)-2-O-BENZOYL-OXIMO-ENDO-3-BORNYL]-(6-METHOXY-5-DECANYL)-SELENIDE
[(1R)-2-BENZOYL-OXIMO-ENDO-3-BORNYL]-(2-METHOXY-1-CYCLOPENTYL)-SELENIDE;MAJOR-ISOMER
cis-1-Methoxy-2-[(2-benzoyloxyoximo-3-bornyl)seleno]cyclopentane
Methyl 5-oxo-3-(thien-2'-yl)-2-(camphorylseleno)hexanoate
2,3,4-TRI-O-ACETYL-6-ALLYLOXYCARBONYLAMINO-1,6-ANHYDRO-6-DEOXY-BETA-D-GLUCOPYRANOSE;MAJOR-ROTAMER
3-hydroxy-1-[3-(1H-imidazol-1-yl)propyl]-4-(4-methylbenzoyl)-5-(3-nitrophenyl)-1,5-dihydro-2H-pyrrol-2-one
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
Other Resources
Unknown Identification

Search your unknown spectrum against the world's largest collection of reference spectra

KnowItAll Campus Solutions

KnowItAll offers faculty and students at your school access to all the tools you need for spectral analysis and structure drawing & publishing! Plus, access the world's largest spectral library.