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ROGIOLOXEPANE-B;(+)-(1S,3R,5R,7R)-3-(1-BROMOPROPYL)-5-CHLORO-7-[(Z)-1-CHLOROHEX-3-EN-5-YNYL]-4,8-DIOXABICYCLO-[5.1.0]-OCTANE

Compound with spectra: 1 NMR

ROGIOLOXEPANE-B;(+)-(1S,3R,5R,7R)-3-(1-BROMOPROPYL)-5-CHLORO-7-[(Z)-1-CHLOROHEX-3-EN-5-YNYL]-4,8-DIOXABICYCLO-[5.1.0]-OCTANE
SpectraBase Compound ID GCUHyHTx7qj
InChI InChI=1S/C15H20BrClO2/c1-3-5-6-7-11(17)13-9-15-14(19-15)8-12(18-13)10(16)4-2/h1,5-6,10-15H,4,7-9H2,2H3/b6-5-/t10-,11+,12-,13-,14+,15-/m1/s1
InChIKey SYCAFZZXXDLZEM-HNLSRTOMSA-N
Mol Weight 347.68 g/mol
Molecular Formula C15H20BrClO2
Exact Mass 346.033521 g/mol
Enantiomer InChIKey SYCAFZZXXDLZEM-WWVNFOFBSA-N

View Spectrum of ROGIOLOXEPANE-B;(+)-(1S,3R,5R,7R)-3-(1-BROMOPROPYL)-5-CHLORO-7-[(Z)-1-CHLOROHEX-3-EN-5-YNYL]-4,8-DIOXABICYCLO-[5.1.0]-OCTANE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
SYNTHETIC-TRANS-KUMAUSYNE
(3-Z,11-Z,7-S*,9-S*,10-R*)-9-ACETOXY-6-CHLORO-7:10-EPOXYPENTADECA-3,11-DIEN-1-YNE
1-[(1S,3S,4S,6R)-6-[(E)-pent-2-en-4-ynyl]-2,5-dioxabicyclo[2.2.1]heptan-3-yl]-4-pentene-2,3-diol
(S)-1-{(2R,3R,6S)-6-[(E)-(R)-2-(tert-Butyl-dimethyl-silanyloxy)-6-methyl-hept-3-enyl]-3-methyl-tetrahydro-pyran-2-yl}-pent-4-en-2-ol
2-BETA-ETHYL-4-BETA-TRIFLUOROACETOXY-3-ALPHA-(2'-METHOXYETHYL)-6-BETA-METHYLTETRAHYDROPYRAN;MAJOR-DIASTEREOMER
5-Ethyl-2,3-epoxy-6,8-dioxabicyclo[3.2.1]octane
ethyl 2-[(4aS,6R,7S,8aR)-7-hydroxy-2,3,4,4a,6,7,8,8a-octahydropyrano[2,3-e]pyran-6-yl]acetate
6,7-Dibromo-N-methyl-9-oxabicyclo[3.3.1]nonan-2-amine
(1'R,2R,4R,6S)-2-Carbomethoxy-4-chloro-6-(1,2-O-methylene-1,2-dihydroxyethyl)terahydropyran
tert-Butyl(2-((2R,3S,6S)-6-((R,E)-2-((tert-butyldimethylsilyl)oxy)-6-methylhept-3-en-1-yl)-3-methyltetrahydro-2H-pyran-2-yl)ethoxy)dimethylsilane
Title Journal or Book Year
On the unusual propensity by the red seaweedLaurencia microcladia of II Rogiolo to form C15 oxepanes: Isolation of rogioloxepane A, B, C, and their likely biogenetic acyclic precursor, prerogioloxepane Helvetica Chimica Acta 1992
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