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[2-R-(E,E)]-1-[2,3-DIHYDRO-3-METHYL-3-[(TRIMETHYLSILYL)-OXY]-2H-PYRAN-2-YL]-2-METHYL-4,6-OCTADIEN-3-ONE

Compound with spectra: 1 NMR

[2-R-(E,E)]-1-[2,3-DIHYDRO-3-METHYL-3-[(TRIMETHYLSILYL)-OXY]-2H-PYRAN-2-YL]-2-METHYL-4,6-OCTADIEN-3-ONE
SpectraBase Compound ID HRhEOaNC7GK
InChI InChI=1S/C18H30O3Si/c1-7-8-9-11-16(19)15(2)14-17-18(3,12-10-13-20-17)21-22(4,5)6/h7-12,15,17H,13-14H2,1-6H3/b8-7+,11-9+/t15-,17+,18?/m0/s1
InChIKey UIVIYVNFYGWOSB-VVMYEPJMSA-N
Mol Weight 322.52 g/mol
Molecular Formula C18H30O3Si
Exact Mass 322.196421 g/mol
Enantiomer InChIKey UIVIYVNFYGWOSB-IATFPMGYSA-N

View Spectrum of [2-R-(E,E)]-1-[2,3-DIHYDRO-3-METHYL-3-[(TRIMETHYLSILYL)-OXY]-2H-PYRAN-2-YL]-2-METHYL-4,6-OCTADIEN-3-ONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
[2-R-(E,E)]-1-[2,3-DIHYDRO-3-METHYL-3-[(TRIMETHYLSILYL)-OXY]-2H-PYRAN-2-YL]-2-METHYL-4,6-OCTADIEN-3-ONE
(2RS,3RS)-3-(5-ETHANOYLTHIABUTYL)-2-PHENYL-3-[(TRIMETHYLSILYL)-OXY]-OXETANE
4a,5,6,7,8,8a-Hexahydro-4a-hydroxy-4-methyl-2H-1-benzopyran-2-one
2-Methoxy-10.alpha.-((trimethylsilyl)oxy)-(1H.beta.,6H.beta.)-bicyclo[4.4.1]undeca-2,4,8-triene
(4R,5S,6S)-5-(Benzyloxy)-6-[[(tert-butyldimethyldimethylsilyl)oxy]methyl]-4-methyltetrahydro-2-pyranone
GONIODIOL_8-MONOACETATE
(2S,3S,6R,4E)-3-TERT-BUTYLDIMETHYLSILYLOXY-6-HYDROXY-1,2-ISOPROPYLIDENDIOXYHENEICOS-4-ENE
(2S,3S,6S,4E)-3-TERT-BUTYLDIMETHYLSILYLOXY-6-HYDROXY-1,2-ISOPROPYLIDENDIOXYHENEICOS-4-ENE
(2RS,3RS)-3-(4-HYDROXYBUTYL)-2-PHENYL-3-[(TRIMETHYLSILYL)-OXY]-OXETANE
(2S,5S)-2-(1,1-Dimethyl-2-propenyl)-5-(tert-butyldiphenylsilyloxymethyl)tetrahydrofuran
Methyl 7-(2-(3-methoxy-1-octenyl)-3-methoxy-5-oxocyclopentyl)heptanoate
Title Journal or Book Year
Stereocontrolled routes to functionalized [1,8-bc]naphthopyran. A study on the total synthesis of quassinoids and tetrahydronaphthalene antibiotics The Journal of Organic Chemistry 1993
[2-R-(E,E)]-1-[2,3-DIHYDRO-3-METHYL-3-[(TRIMETHYLSILYL)-OXY]-2H-PYRAN-2-YL]-2-METHYL-4,6-OCTADIEN-3-ONE
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