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11-BROMOMETHYLIDENE-12-OXAPENTACYCLO-[5.4.1.0(2,6).0(3,9).0(8,10)]-DODEC-4-ENE

Compound with spectra: 1 NMR

11-BROMOMETHYLIDENE-12-OXAPENTACYCLO-[5.4.1.0(2,6).0(3,9).0(8,10)]-DODEC-4-ENE
SpectraBase Compound ID 1P2HCVHnSHH
InChI InChI=1S/C12H11BrO/c13-3-6-9-8-4-1-2-5-7(4)12(6)14-11(5)10(8)9/h1-5,7-12H/b6-3+/t4-,5+,7-,8-,9+,10-,11-,12-/m0/s1
InChIKey WJXHEGQYSYIDPI-GCVBDFGXSA-N
Mol Weight 251.12 g/mol
Molecular Formula C12H11BrO
Exact Mass 249.999328 g/mol
Enantiomer InChIKey WJXHEGQYSYIDPI-FKOVWSPXSA-N

View Spectrum of 11-BROMOMETHYLIDENE-12-OXAPENTACYCLO-[5.4.1.0(2,6).0(3,9).0(8,10)]-DODEC-4-ENE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(2S)-4-Bromo-1,2-dehydro-6.beta.,10.alpha.,11.beta.-alpha.-santonin
(3S,3aS,5aS,7S,9bS)-7-hydroxy-3,5a,9-trimethyl-3a,4,5,6,7,9b-hexahydro-3H-benzo[g]benzofuran-2,8-quinone
3b,4a,7,7a,7b,7c,7D,8,8a,8b-Decahydro-1H-4-oxa-dipentaleno(1,2,3-cd:1',2',3'-gh)pentalene-2,6-dione
14-Hydroxy-4-oxapentacyclo[7.6.0.0(2,7).0(6,10).0(11,15)]pentadecan-12-en-3,5-dione
#3;CRYPTOPORIC-ACID-J;(2R,3S)-2-[[(1S*,4AR*,5R*,8AS*)-5-(HYDROXYMETHYL)-5,8A-DIMETHYL-2-METHYLENEDECAHYDRO-NAPHTHALEN-1-YL]-METHOXY]-3-(METHOXYCARBONYL)-PENTAN
1H-2-Benzopyran-1-acetic acid, 3-(2,5-dihydro-2-methyl-5-oxo-2-furanyl)-3,4,4a,7,8,8a-hexahydro-7-hydroxy-5-methyl-8-(1-methylethyl)-, methyl ester, [1.alpha.,3.alpha.(R*),4a.alpha.,7.beta.,8.alpha.,8a.alpha.]-
syn-2,3,13,14-Tetra(methoxycarbonyl)-7,7'-dioxabisbicyclo[2.2.1]hept-2-eno[5,6-b:5',6'-b']bisbicyclo[2.2.2]oct-7-eno[5,6-b:5',6'-f]tricyclo[4.2.0.0(2,5)]octane
11-Oxatetracyclo[4.2.1.1(2,5).1(7,10)]undec-3-ene, 9-methoxy-9-methyl-
18-METHYLMALONYL-7-ALPHA-HYDROXY-METHYLTRINERACETAL
3-HYDROXYISOPHOTOSANTONIN;MAJOR-ISOMER
Title Journal or Book Year
Synthesis and Chemical Transformations of 4, 5-Homosnoutene Derivatives: An Attempted New Access onto the (CH)12 Energy Hypersurface Helvetica Chimica Acta 1990
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