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DIMETHYL-(1'R*,2'R*,2''S*,3'R*)-[2'-(3''-BrOMO-2''-TRIMETHYLSILYLOXYPROPYL)-3'-METHOXYMETHYLOXY-2'-METHYLCYClOHEXYL]-MALONATE

Compound with spectra: 1 NMR, and 1 MS (GC)

DIMETHYL-(1'R*,2'R*,2''S*,3'R*)-[2'-(3''-BrOMO-2''-TRIMETHYLSILYLOXYPROPYL)-3'-METHOXYMETHYLOXY-2'-METHYLCYClOHEXYL]-MALONATE
SpectraBase Compound ID EGVIfym4C1L
InChI InChI=1S/C20H37BrO7Si/c1-20(11-14(12-21)28-29(5,6)7)15(9-8-10-16(20)27-13-24-2)17(18(22)25-3)19(23)26-4/h14-17H,8-13H2,1-7H3/t14-,15-,16-,20-/m1/s1
InChIKey RZPKDXAWJMCLAT-AXHMDWHKSA-N
Mol Weight 497.5 g/mol
Molecular Formula C20H37BrO7Si
Exact Mass 496.149193 g/mol
Enantiomer InChIKey RZPKDXAWJMCLAT-ULMVMLMRSA-N

View Spectrum of DIMETHYL-(1'R*,2'R*,2''S*,3'R*)-[2'-(3''-BrOMO-2''-TRIMETHYLSILYLOXYPROPYL)-3'-METHOXYMETHYLOXY-2'-METHYLCYClOHEXYL]-MALONATE

MS (GC) Spectrum
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Source of Spectrum B-48-609-0

View Spectrum of DIMETHYL-(1'R*,2'R*,2''S*,3'R*)-[2'-(3''-BrOMO-2''-TRIMETHYLSILYLOXYPROPYL)-3'-METHOXYMETHYLOXY-2'-METHYLCYClOHEXYL]-MALONATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • 2-[(1R,2R,3R)-2-[(2R)-3-bromo-2-trimethylsilyloxy-propyl]-3-(methoxymethoxy)-2-methyl-cyclohexyl]malonic acid dimethyl ester
2-[(1R,2R,3R)-2-[(2S)-3-bromo-2-trimethylsilyloxy-propyl]-3-(methoxymethoxy)-2-methyl-cyclohexyl]malonic acid dimethyl ester
DIMETHYL-(1'R*,2'R*,2''R*,3'R*)-[2'-(3''-BrOMO-2''-TRIMETHYLSILYLOXYPROPYL)-3'-METHOXYMETHYLOXY-2'-METHYLCYClOHEXYL]-MALONATE
Methyl 1-Methyl-4-oxo-9-t-butoxybicyclo[4.3.0]nonan-5-carboxylate
METHYL-(+/-)-1-BETA-TERT.-BUTOXY-7A-BETA-METHYL-5-OXO-2,3,3A-ALPHA,4,5,6,7,7A-OCTAHYDRO-1H-INDENE-4-ALPHA-CARBOXYLATE
1-(5-Hexenyl)-6-methoxy-3-(methoxycarbonyl)bicyclo[3.3.0]octan-2-one
(4a.alpha.,5.alpha.,8.alpha.,8a.beta.)-octahydro-8-hydroxy-5-(methoxymethoxy)-4a,8-dimethyl-2(1H)-naphthalenone
Cyclohexanepropanoic acid, 3-(acetyloxy)-6-(methoxycarbonyl)-2,2,6-trimethyl-, methyl ester, [1S-(1.alpha.,3.alpha.,6.beta.)]-
Cyclohexanepropanoic acid, 3-(acetyloxy)-6-(methoxycarbonyl)-2,2,6-trimethyl-, methyl ester, [1R-(1.alpha.,3.beta.,6.alpha.)]-
[(2R*,4aR*,5S*,8aS*)-2-tert-Butyldimethylsilyloxy-5-(1,3,6-trioxaheptyl)-1,2,4a,5,6,7,8,8a-octahydro-4a-naphthyl]methanol
4,4,8,8(1H,5H)-Azulenetetracarboxylic acid, hexahydro-2,2-dimethoxy-, tetramethyl ester, trans-
Title Journal or Book Year
Synthetic Studies on Wedeligenin: Preparation of an A/B-Ring Intermediate Australian Journal of Chemistry 1995
Other Resources
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