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[(1R)-2-OXIMO-ENDO-3-BORNYL]-[METHYLENE-(2,3-DIHYDRO-BENZOFURAN-2-YL)]-SELENIDE;MAJOR-ISOMER

Compound with spectra: 2 NMR

[(1R)-2-OXIMO-ENDO-3-BORNYL]-[METHYLENE-(2,3-DIHYDRO-BENZOFURAN-2-YL)]-SELENIDE;MAJOR-ISOMER
SpectraBase Compound ID JRGCjygfzhH
InChI InChI=1S/C19H25NO2Se/c1-18(2)14-8-9-19(18,3)17(20-21)16(14)23-11-13-10-12-6-4-5-7-15(12)22-13/h4-7,13-14,16,21H,8-11H2,1-3H3/b20-17-/t13?,14-,16-,19-/m1/s1
InChIKey HBTLHSTVGWDHSH-KEYNEDQMSA-N
Mol Weight 378.39 g/mol
Molecular Formula C19H25NO2Se
Exact Mass 379.105051 g/mol
Enantiomer InChIKey HBTLHSTVGWDHSH-YUNWLRSUSA-N

View Spectrum of [(1R)-2-OXIMO-ENDO-3-BORNYL]-[METHYLENE-(2,3-DIHYDRO-BENZOFURAN-2-YL)]-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]-[METHYLENE-(2,3-DIHYDRO-BENZOFURAN-2-YL)]-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]-[METHYLENE-(2,3-DIHYDRO-BENZOFURAN-2-YL)]-SELENIDE;MINOR-ISOMER
2-[(2-Oximo-3-selenobornyl)methyl]-2,3-dihydrobenzofuran
8,11,11-Trimethyl-3-oxa-6-azatricyclo[6.2.1.0(2,7)]undec-6-en-4-one
GNAPHALIOL-9-O-BETA-D-GLUCOPYRANOSIDE
N-tert-Butyl-10-[2-(1-(tert-butyloxycarbonyl)propyl)imino-7,7-dimethylcyclo[2.2.1]heptyl)methyl]sulfonamide isomer
(1S,4aR,6E,8aS)-6-hydroximino-5,5,8a-trimethyl-2-methylene-decalin-1-carboxylic acid methyl ester
5-pyrimidinecarboxylic acid, 1,2,3,4-tetrahydro-1-methyl-4-(4-methylphenyl)-6-(4-morpholinylmethyl)-2-oxo-, ethyl ester
3-pyridinecarboxylic acid, 1,4,5,6-tetrahydro-2-methyl-4-[2-(1-methylethoxy)phenyl]-6-oxo-, 2-phenylethyl ester
1-ACETYL-4-TERT.-BUTYL-2,3,6-TRI-TERT.-BUTYL-THIO-1,2,3,6-TETRAHYDRO-PYRIDINE;(ROTAMER-#1)
1-BETA-HYDROXY-7-ALPHA-H,11-ALPHA-H-EUDESM-4(15)-EN-12,8-BETA-LACTONE
(+/-)-2-(1-ADAMANTYL)-4-ACETYL-5-[5-(4-METHYLPHENYL-3-ISOXAZOLYL)]-1,3,4-OXADIAZOLINE
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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