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(4S,5R,6S)-4-CYCLOHEXYL-3-METHYL-5-(2-PROPENYL)-6-[(1R,2S)-(2-PHENYLCYCLOHEXYL)-OXY]-5,6-DIHYDRO-4H-[1,2]-OXAZINE-2-OXIDE

Compound with spectra: 1 NMR

(4S,5R,6S)-4-CYCLOHEXYL-3-METHYL-5-(2-PROPENYL)-6-[(1R,2S)-(2-PHENYLCYCLOHEXYL)-OXY]-5,6-DIHYDRO-4H-[1,2]-OXAZINE-2-OXIDE
SpectraBase Compound ID JFDjUttmFHd
InChI InChI=1S/C26H37NO3/c1-3-12-23-25(21-15-8-5-9-16-21)19(2)27(28)30-26(23)29-24-18-11-10-17-22(24)20-13-6-4-7-14-20/h3-4,6-7,13-14,21-26H,1,5,8-12,15-18H2,2H3/t22-,23-,24-,25+,26+/m1/s1
InChIKey PBQZKWDJFVNJAE-OYHZZYGJSA-N
Mol Weight 411.6 g/mol
Molecular Formula C26H37NO3
Exact Mass 411.277344 g/mol
Enantiomer InChIKey PBQZKWDJFVNJAE-QWDLEPIUSA-N

View Spectrum of (4S,5R,6S)-4-CYCLOHEXYL-3-METHYL-5-(2-PROPENYL)-6-[(1R,2S)-(2-PHENYLCYCLOHEXYL)-OXY]-5,6-DIHYDRO-4H-[1,2]-OXAZINE-2-OXIDE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(4R,6S)-CIS-4-(4''-CHLOROPHENYL)-6-(2'-ISOCARANOXY)-5,6-DIHYDRO-4H-1,2-OXAZINE-3-CARBONITRILE-2-OXIDE
4-((5S,6S,9R)-6-Isopropyl-4,9-dimethyl-1,3-dioxaspiro[4.5]decan-2-yl)-2-methoxyphenol
JATAMANIN-C
(2S,3S)-5-Methyl-2-(1-methyl-1-phenylethyl)cyclohexyl 2-hydroxy-2-(2-oxo-5-tert-butylcyclohexyl)propanoate
3,6-Methanobenzofuran-8-carboxylic acid, octahydro-7-hydroxy-2-oxo-, (3.alpha.,3a.beta.,6.alpha.,7.alpha.,7a.beta.,8S*)-(.+-.)-
(1S,8aS)-2,5,5,8a-Tetramethyl-1,4,4a,5,6,7,8,8a-octahydro-naphthalene-1-carboxylic acid (R)-2-acetoxy-3-(tert-butyl-dimethyl-silanyloxy)-propyl ester
(1R*,2R*,6R*,E)-1-Acetoxy-2,6-diphenyl-2-(2-triethylsilylethenyl)cyclohexane
(4S,6R)-CIS-4-(4''-CHLOROPHENYL)-6-(2'-ISOPINOCANPHOXY)-5,6-DIHYDRO-4H-1,2-OXAZINE-3-CARBONITRILE-2-OXIDE
(4R,6R)-TRANS-4-(4''-CHLOROPHENYL)-6-(2'-ISOPINOCANPHOXY)-5,6-DIHYDRO-4H-1,2-OXAZINE-3-CARBONITRILE-2-OXIDE
(2R,3R)-Methyl 5-oxo-3-[4-(dimethylamino)phenyl]-2-phenyltetrahydrofuran-2-carboxylate isomer
Title Journal or Book Year
Tandem Inter [4 + 2]/Intra [3 + 2] Cycloadditions of Nitroalkenes. Asymmetric Synthesis of Highly Functionalized Aminocyclopentanes Using the Bridged Mode (β-Tether) Process The Journal of Organic Chemistry 1998
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