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

*Links on SpectraBase are not permalinks.

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

Compound with spectra: 2 NMR

[(1R)-2-BENZOYL-OXIMO-ENDO-3-BORNYL]-(ALPHA-METHYL-2-TETRAHYDROFURFURYL)-SELENIDE;MAJOR-ISOMER
SpectraBase Compound ID GEHTKj2JnbN
InChI InChI=1S/C23H31NO3Se/c1-15(18-11-8-14-26-18)28-19-17-12-13-23(4,22(17,2)3)20(19)24-27-21(25)16-9-6-5-7-10-16/h5-7,9-10,15,17-19H,8,11-14H2,1-4H3/b24-20-/t15?,17-,18?,19-,23-/m1/s1
InChIKey NQGYOAGYCCHGPY-GCEYBIKUSA-N
Mol Weight 448.48 g/mol
Molecular Formula C23H31NO3Se
Exact Mass 449.146916 g/mol
Enantiomer InChIKey NQGYOAGYCCHGPY-KVBQSZIZSA-N

View Spectrum of [(1R)-2-BENZOYL-OXIMO-ENDO-3-BORNYL]-(ALPHA-METHYL-2-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]-(ALPHA-METHYL-2-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]-(ALPHA-METHYL-2-TETRAHYDROFURFURYL)-SELENIDE;MINOR-ISOMER
[(1R)-2-BENZOYL-OXIMO-ENDO-3-BORNYL]-[METHYLENE-(2,3-DIHYDRO-BENZOFURAN-2-YL)]-SELENIDE;MAJOR-ISOMER
[(1R)-2-BENZOYL-OXIMO-ENDO-3-BORNYL]-(2-METHYL-2-METHOXY-2-PHENYL-1-ETHYL)-SELENIDE;MAJOR-ISOMER
(1R,2E)-3-[(2-methoxy-2-phenylpropyl)selanyl]-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one O-benzoyloxime
6-BETA-ACETOXY-4-ALPHA,11-DIHYDROXYEUDESMAN-1-ONE
5F-MDMB-PINACA TMS
(5Z)-5-({1-[3-(4-chloro-3-methylphenoxy)propyl]-1H-indol-3-yl}methylene)-1-(4-fluorophenyl)-2,4,6(1H,3H,5H)-pyrimidinetrione
Benzoylhenryoside
2,2,4,4-tetramethyl-3-pentyl trans-decahydro-6.beta.-[tert-butyldimethylsilyl)oxy]-5,5,8a.beta.-trimethyl-2-methylene-1.xi.-naphthalenecarboxylate
1-BROMOMAALIOXIDE
3,4-Dihydro-2-methyl-4-oxo-3,3-bis[(2E,7R,11R)-3,7,11,15-tetramethylhexadec-2-enyl]naphth-1-yl Acetate
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.