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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 © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
2,3-BIS-(TERT.-BUTYL-DIMETHYL-SILOXY)-5-PHENYL-3-(2-PHENYL-ETHENYL)-CYCLOPENT-1-ENE
4-exo-Benzoyloxy-1R-(T-butyl-dimethyl-silyloxy)-6-oxa-bicyclo(3.2.1)oct-2-en-7-one
4-Benzyl-7-methoxy-3-phenylcoumarin
Cyclopenta[C][1]benzopyran-4(1H)-one, 2,3-dihydro-6-methyl-7-[(3-methyl-2-butenyl)oxy]-
(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
(4AR, 9R,12S)-3,4,8,9,10,11-hexahydro-12-(T-butyl-dimethyl-siloxy)-4a,9-methano-4ah-benzo-cyclononen-2(5H)-one
5,7-Dimethoxy-4-(2,5-dimethoxyphenyl)-2H-1-benzopyran-2-one
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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