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(1S*,3R*,7R*,9S*,10S*,12R*,14R*)-10-HYDROXY-12-(2'-FORMYL)-ALLYL-7-METHYL-3-PENTYL-2,8,13-TRIOXATRICYCLO-[8.5.0.0(9,14)]-PENTADECANE

Compound with spectra: 1 NMR

(1S*,3R*,7R*,9S*,10S*,12R*,14R*)-10-HYDROXY-12-(2'-FORMYL)-ALLYL-7-METHYL-3-PENTYL-2,8,13-TRIOXATRICYCLO-[8.5.0.0(9,14)]-PENTADECANE
SpectraBase Compound ID K9sktq24Yq1
InChI InChI=1S/C22H36O5/c1-4-5-6-8-16-9-7-10-22(3)20(26-16)13-19-21(27-22)18(24)12-17(25-19)11-15(2)14-23/h14,16-21,24H,2,4-13H2,1,3H3/t16-,17-,18+,19-,20+,21+,22-/m1/s1
InChIKey QPJKBVOOKRBDJO-YSNDBMGOSA-N
Mol Weight 380.5 g/mol
Molecular Formula C22H36O5
Exact Mass 380.256274 g/mol
Enantiomer InChIKey QPJKBVOOKRBDJO-LPLVAOHZSA-N

View Spectrum of (1S*,3R*,7R*,9S*,10S*,12R*,14R*)-10-HYDROXY-12-(2'-FORMYL)-ALLYL-7-METHYL-3-PENTYL-2,8,13-TRIOXATRICYCLO-[8.5.0.0(9,14)]-PENTADECANE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(1S*,3R*,7R*,9S*,10S*,12R*,14R*)-10-HYDROXY-12-HYDROXYALLYLMETHYL-7-METHYL-3-PENTYL-2,8,13-TRIOXATRICYCLO-[8.5.0.0(9,14)]-PENTADECANE
(1S*,3R*,7R*,9S*,10S*,12R*,14R*)-12-ACETOXYALLYLMETHYL-10-HYDROXY-7-METHYL-3-PENTYL-2,8,13-TRIOXATRICYCLO-[8.5.0.0(9,14)]-PENTADECANE
(1S*,3R*,7R*,9S*,10S*,12R*/12S*14R*)-10-HYDROXY-12-METHOXY-7-METHYL-3-PENTYL-2,8,13-TRIOXATRICYCLO-[8.5.0.0(9,14)]-PENTADECANE;MAJOR-ISOMER
(1S*,3R*,7R*,9S*,10S*,14R*)-10-HYDROXY-7-METHYL-3-PENTYL-2,8,13-TRIOXATRICYCLO-[8.5.0.0(9,14)]-PENTADECANE-12-ONE
2,3,4,6-Tetra-o-methyl-.beta.-D-glucopyranosyl 4,6-di-o-methyl-1,2,5-tri-o-TMS-D-galactitol
D-Gluco-Octitol, 3,7-anhydro-1,4-dideoxy-2-C-methyl-, 5,6,8-triacetate 2-(3,5-dinitrobenzoate)
CUSCUTIC-ACID-D
7,8-secoeupalmerin-15-carboxylic acid methyl ester
FJDXMYNEHWZSGG-WUXXAJNRSA-N
ISOACTEOSIDE;FRACTION-II
Title Journal or Book Year
Development of an Approach to the Synthesis of the ABC Ring System of Hemibrevetoxin B Organic Letters 2006
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