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(1RS,2RS,3RS,4SR,7RS,8SR,10SR)-3-Methyl-5,11-dioxatetracyclo[5.5.0.0(2,10).0(4,8)]dodecane

Compound with spectra: 1 NMR

(1RS,2RS,3RS,4SR,7RS,8SR,10SR)-3-Methyl-5,11-dioxatetracyclo[5.5.0.0(2,10).0(4,8)]dodecane
SpectraBase Compound ID EP5XAcyl9ob
InChI InChI=1S/C11H16O2/c1-5-10-8-4-12-9(10)2-6-7(8)3-13-11(5)6/h5-11H,2-4H2,1H3/t5-,6-,7-,8+,9-,10-,11-/m0/s1
InChIKey BQNWNHUYYGZNSK-OOJKNYCESA-N
Mol Weight 180.25 g/mol
Molecular Formula C11H16O2
Exact Mass 180.11503 g/mol
Enantiomer InChIKey BQNWNHUYYGZNSK-XBQSJFCKSA-N

View Spectrum of (1RS,2RS,3RS,4SR,7RS,8SR,10SR)-3-Methyl-5,11-dioxatetracyclo[5.5.0.0(2,10).0(4,8)]dodecane

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(1RS,2RS,3RS,4SR,7RS,8SR,10SR)-3-Methyl-5,11-dioxatetracyclo[5.5.0.0(2,10).0(4,8)]dodecane
4-.beta.-Methyl-3,11-dioxatetracyclo[6.3.0.0(2,6).0(5,9)]undecane
3,8,13-Trioxaoctacyclo[13.2.2.2(6,10).0(2,14).0(4,17).0(5,11).0(7,9).0(12,16)]uneicosane
exo-9-Bromo-7-oxa-tetracyclo(6.3.0.0.0)undecane
9-EXO-BROM-7-OXATETRACYCLO-[6.3.0.0(2,6).0(3,10)]-UNDECAN
((R)-5-Butyl-2-iodo-4-oxa-tricyclo[4.2.1.0*3,7*]non-9-yl)-methanol
5,3,7-[1,2,3]Propanetriylbenzofuran-2(3H)-one, hexahydro-10-hydroxy-
1,4:5,8-Dimethanonaphthalen-2-ol, decahydro-9-(phenylmethoxy)-, (1.alpha.,2.alpha.,4.alpha.,4a.alpha.,5.beta.,8.beta.,8a.alpha.,9R*)-
ENDO-4-CYANO-EXO-9,10-EPOXYTETRACYCLO-[6.2.1.1-(3.6).0-(2.7)]-DODECENE
9-EXO-CHLOR-7-OXATETRACYCLO-[6.3.0.0(2,6).0(3,10)]-UNDECAN
exo-9-Chloro-7-oxa-tetracyclo(6.3.0.0.0)undecane
Title Journal or Book Year
Ether formation by intramolecular attack of hydroxy on cyclopropyl rings: a model for the formation of the tetrahydrofuran moiety in the diterpenoid, harringtonolide Journal of the Chemical Society, Perkin Transactions 1 1998
(1RS,2RS,3RS,4SR,7RS,8SR,10SR)-3-Methyl-5,11-dioxatetracyclo[5.5.0.0(2,10).0(4,8)]dodecane
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