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RAC-(4R,5R,6S)-6-ETHYL-6-HYDROXY-4-[DIMETHYL-(PHENYL)-SILYL]-2-OXA-SPIRO-[4.4]-NONAN-1-ONE

Compound with spectra: 1 NMR

RAC-(4R,5R,6S)-6-ETHYL-6-HYDROXY-4-[DIMETHYL-(PHENYL)-SILYL]-2-OXA-SPIRO-[4.4]-NONAN-1-ONE
SpectraBase Compound ID 2MlDkSZ1rnR
InChI InChI=1S/C18H26O3Si/c1-4-17(20)11-8-12-18(17)15(13-21-16(18)19)22(2,3)14-9-6-5-7-10-14/h5-7,9-10,15,20H,4,8,11-13H2,1-3H3/t15-,17+,18-/m0/s1
InChIKey CNVLSBGFMJCTHC-JQHSSLGASA-N
Mol Weight 318.49 g/mol
Molecular Formula C18H26O3Si
Exact Mass 318.165121 g/mol
Enantiomer InChIKey CNVLSBGFMJCTHC-BPQIPLTHSA-N

View Spectrum of RAC-(4R,5R,6S)-6-ETHYL-6-HYDROXY-4-[DIMETHYL-(PHENYL)-SILYL]-2-OXA-SPIRO-[4.4]-NONAN-1-ONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
RAC-(4R,5S,6S)-4-[DIMETHYL-(PHENYL)-SILYL]-6-HYDROXY-6-(PENT-4-EN-1-YL)-2-OXASPIRO-[4.4]-NONAN-1-ONE
RAC-METHYL-4-[(4R,5S,6R)-4-[DIMETHYL-(PHENYL)-SILYL]-6-HYDROXY-1-OXO-2-OXASPIRO-[4.4]-NONAN-6-YL]-BUTANOATE
RAC-(4R,5S,6S)-4-[DIMETHYL-(PHENYL)-SILYL]-6-HYDROXY-6-METHYL-2-OXASPIRO-[4.4]-NONAN-1-ONE
N-Benzyl-(2R,3R,4R,4aS,8aR)-3,4-O-isopropylidene-2-methoxymethyl-4a,8a-decahydroquinoline
C24 D13(14)-monounsaturated tricyclic terpene
(1RS,4aRS,5SR,8aSR)-1-(3-furyl)-4a-hydroxy-5,8a-dimethyloctahydro-2-benzopyran-3-one
7-Amino-3-cyano-2-methoxy-4,6-diphenyl-1,8-naphthyridine
methyl (1S,4aR,5S)-5-[2-(2-{[(4-chlorobenzoyl)oxy]methyl}-3-furyl)ethyl]-1,4a-dimethyl-6-methylenedecahydro-1-naphthalenecarboxylate
ETHYL-(1R*,5S*,9S*)-5-(3-BUTENYL)-9-HYDROXY-3-(3-PHENYLPROPYL)-9-(2-PROPENYL)-3-AZABICYCLO-[3.3.1]-NONANE-1-CARBOXYLATE
ETHYL-(1R*,5S*,9R*)-5-(3-BUTENYL)-9-HYDROXY-3-(3-PHENYLPROPYL)-9-(2-PROPENYL)-3-AZABICYCLO-[3.3.1]-NONANE-1-CARBOXYLATE
Title Journal or Book Year
Development of an additive-controlled, SmI2-mediated stereoselective sequence: Telescoped spirocyclisation, lactone reduction and Peterson elimination Beilstein Journal of Organic Chemistry 2013
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