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

Compound with spectra: 3 NMR

[(1R)-2-BENZOYL-OXIMO-ENDO-3-BORNYL]-(1,2-DIPHENYL-2-METHOXY-1-ETHYL)-SELENIDE;MAJOR-ISOMER
SpectraBase Compound ID 61jZzMEmWYw
InChI InChI=1S/C32H35NO3Se/c1-31(2)25-20-21-32(31,3)29(33-36-30(34)24-18-12-7-13-19-24)28(25)37-27(23-16-10-6-11-17-23)26(35-4)22-14-8-5-9-15-22/h5-19,25-28H,20-21H2,1-4H3/b33-29-/t25-,26?,27?,28-,32-/m1/s1
InChIKey FISMVGHQSQEUMY-DUUWYRRWSA-N
Mol Weight 560.6 g/mol
Molecular Formula C32H35NO3Se
Exact Mass 561.178216 g/mol
Enantiomer InChIKey FISMVGHQSQEUMY-LLNJTYLKSA-N

View Spectrum of [(1R)-2-BENZOYL-OXIMO-ENDO-3-BORNYL]-(1,2-DIPHENYL-2-METHOXY-1-ETHYL)-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]-(1,2-DIPHENYL-2-METHOXY-1-ETHYL)-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]-(1,2-DIPHENYL-2-METHOXY-1-ETHYL)-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]-(1,2-DIPHENYL-2-METHOXY-1-ETHYL)-SELENIDE;MINOR-ISOMER
  • [(1R)-2-BENZOYL-OXIMO-ENDO-3-BORNYL]-(1,2-DIPHENYL-2-METHOXY-1-ETHYL)-SELENIDE
[(1R)-2-BENZOYL-OXIMO-ENDO-3-BORNYL]-(2-METHOXY-2-METHYL-1-CYCLOHEXYL)-SELENIDE
4,9-DIMETHOXY-7,7-BIS-(TRIFLUOROMETHYL)-7H-FURO-[3,2-G]-CHROMENE
3-quinolinecarbonitrile, 4-(1,3-benzodioxol-5-yl)-1,4,5,6,7,8-hexahydro-2-(methylthio)-5-oxo-
ethyl 7-(4-bromophenyl)-2-[(2-fluorobenzyl)sulfanyl]-5-methyl-4,7-dihydro[1,2,4]triazolo[1,5-a]pyrimidine-6-carboxylate
(+-)-(3a.alpha.,6.alpha.,7.beta.,9a.beta.)-2,3,6,7,8,9-Hexahydro-6-methyl-3a,6-epoxy-7,9a-methano-1H-cyclopentacycloocten-10-one
10-(3,4-dichlorophenyl)-2,3-dihydro-1H-imidazo[1,2-g][1,6]naphthyridin-5-one
AGI-B4;7,8-DIHYDROXANTHENONE-8-CARBOXYLIC-ACID-METHYLESTER
3-(3-nitrophenyl)-1-(2-pyridinylmethoxy)-2(1H)-quinoxalinone 4-oxide
5,3'-DIHYDROXY-4'-METHOXY-2'',2''-DIMETHYLPYRANO-[5'',6'':8,7]-ISOFLAVONE
1H-indole, 2-methyl-1-[2-oxo-2-(1-pyrrolidinyl)ethyl]-3-[1,2,3,6-tetrahydro-1-[(phenylmethyl)sulfonyl]-4-pyridinyl]-
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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