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METHYL-E-3-[1-TERT.-BUTYL-DIMETHYL-SILOXY-2-METHOXY-4-(2-FURYL)-CYCLOPENT-2-EN-1-YL]-PROPENOATE

Compound with spectra: 1 NMR

METHYL-E-3-[1-TERT.-BUTYL-DIMETHYL-SILOXY-2-METHOXY-4-(2-FURYL)-CYCLOPENT-2-EN-1-YL]-PROPENOATE
SpectraBase Compound ID 8iRML6iqNb5
InChI InChI=1S/C20H30O5Si/c1-19(2,3)26(6,7)25-20(11-10-18(21)23-5)14-15(13-17(20)22-4)16-9-8-12-24-16/h8-13,15H,14H2,1-7H3/b11-10+/t15-,20+/m0/s1
InChIKey YLXXOMNJRYCFSX-GYIJXDSHSA-N
Mol Weight 378.54 g/mol
Molecular Formula C20H30O5Si
Exact Mass 378.186251 g/mol
Enantiomer InChIKey YLXXOMNJRYCFSX-UELALMBDSA-N

View Spectrum of METHYL-E-3-[1-TERT.-BUTYL-DIMETHYL-SILOXY-2-METHOXY-4-(2-FURYL)-CYCLOPENT-2-EN-1-YL]-PROPENOATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(2R,4R,7S,8S,9S)-11-[(Allyloxycarbonyl)amino]-7,8-epoxy-2,4-dimethyl-1,5-dioxaspiro[5.5]non-10-en-9-ol
exo-(2-Hydroxyphenyl)(1,2,3,4-tetrahydro-1,4-epoxynaphthalen-2-yl)methanone
1-{6-Chloro-1-[(4-methylphenyl)sulfonyl]-1H-indol-2-yl}butan-2-one
2-[(2R,4aR,5R,8E,8aS)-5-[tert-butyl(dimethyl)silyl]oxy-8-(methoxymethylene)-4a-methyl-decalin-2-yl]propan-2-ol
cyclopenta[c][1]benzopyran-4(1H)-one, 2,3-dihydro-6-methyl-7-(2-propenyloxy)-
5,7-Dimethoxy-4-(2,5-dimethoxyphenyl)-2H-1-benzopyran-2-one
(Z)-(1R,3R,5R)-1-Acetoxy-3-[(tert-butyldimethylsilyl)oxy]-6-oxa-4-[3'-(methoxymethoxy)propylidene]bicyclo[3.2.1]octan-7-one
(E)-(1R,3R,5R)-1-Acetoxy-3-[(tert-butyldimethylsilyl)oxy]-6-oxa-4-[3'-(methoxymethoxy)propylidene]bicyclo[3.2.1]octan-7-one
2-[(benzyloxy)carbonyl]-3-[((benzyloxy)carbonyl)-methyl]-5-methyl-1-(2-methylpent-4-en-2-yl)-4-imidazolidinone
CHIRATOL;1,5-DIHYDROXY-3,8-DIMETHOXY-XANTHONE
Title Journal or Book Year
Reactions of Fischer Carbene Complexes with Siloxydienes: Formation of Cycloheptadiene and Cyclopentene Derivatives—Formal [2+1] Cycloaddition Followed by Cope Rearrangement Versus Formal [3+2] Cycloaddition with or without Preceding Carbene-Ligand Metathesis Chemistry - A European Journal 1999
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