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Obtention of the Lactone 14 from the Allyl Derivative 6.(1RS,2SR)-2-[2-(tert-Butyldimethylsiloxy)-5-oxocyclohexl-yl]ethanal

Compound with spectra: 1 MS (GC)

Obtention of the Lactone 14 from the Allyl Derivative 6.(1RS,2SR)-2-[2-(tert-Butyldimethylsiloxy)-5-oxocyclohexl-yl]ethanal
SpectraBase Compound ID ieVbojs3GF
InChI InChI=1S/C14H26O3Si/c1-14(2,3)18(4,5)17-13-7-6-12(16)10-11(13)8-9-15/h9,11,13H,6-8,10H2,1-5H3
InChIKey DNIZJQQVWNOGSB-UHFFFAOYSA-N
Mol Weight 270.44 g/mol
Molecular Formula C14H26O3Si
Exact Mass 270.165121 g/mol

View Spectrum of Obtention of the Lactone 14 from the Allyl Derivative 6.(1RS,2SR)-2-[2-(tert-Butyldimethylsiloxy)-5-oxocyclohexl-yl]ethanal

MS (GC) Spectrum
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Source of Spectrum J-56-394-13
Cyclohexanone, 4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3-(2-propenyl)-, cis-(.+-.)-
(3SR,4RS)-4-Allyl-3-(tert-butyldimethylsiloxy)cyclopentanone
Methyl 3-(t-Butyldimethylsiloxy)-3-cyclohexylpropanoate
Ethyl 3-(t-Butyldimethylsiloxy)-3-cyclopentylpropanoate
4-Butyl-5-tert-butyldimethylsilyloxy-2-methyl-2-nonene
(3S,4R)-3-(tert-Butyldimethylsilyloxy)-4,7-dimethyloct-6-enoic methyl ester
(2R*,3S*)-3-(tert-Butyldimethylsiloxy)-2'-(iodomethyl)oxepane
3-[(2R,3S)-3-(tert-Butyldimethylsilyloxy)tetrahydropyran-2-yl]propen-1-ol
(1R,2S)-(+)-2-[(Thexyldimethylsilyl)oxy]-1-cyclopentanecarboxaldehyde
(4R,5R,6S)-5-((tert-Butyldimethylsilyl)oxy)-4,6-dimethyloctan-3-ol
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