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(2R,3S,4R,5R,6R,7S,8R)-4,5-(CYCLOHEXYLIDENEDIOXY)-3-HYDROXY-2,4,6-TRIMETHYLNONAN-8-OLID-7-YL-(E)-(R)-4-HYDROXY-2-OCTENOATE

Compound with spectra: 2 NMR

(2R,3S,4R,5R,6R,7S,8R)-4,5-(CYCLOHEXYLIDENEDIOXY)-3-HYDROXY-2,4,6-TRIMETHYLNONAN-8-OLID-7-YL-(E)-(R)-4-HYDROXY-2-OCTENOATE
SpectraBase Compound ID 9FJHpLvWiDW
InChI InChI=1S/C26H42O8/c1-6-7-11-19(27)12-13-20(28)32-21-16(2)23-25(5,22(29)17(3)24(30)31-18(21)4)34-26(33-23)14-9-8-10-15-26/h12-13,16-19,21-23,27,29H,6-11,14-15H2,1-5H3/b13-12+/t16-,17-,18-,19-,21+,22+,23-,25-/m1/s1
InChIKey YTAONFQDZPGONZ-LGAOGKDQSA-N
Mol Weight 482.6 g/mol
Molecular Formula C26H42O8
Exact Mass 482.287968 g/mol
Enantiomer InChIKey YTAONFQDZPGONZ-FRZVNYJRSA-N

View Spectrum of (2R,3S,4R,5R,6R,7S,8R)-4,5-(CYCLOHEXYLIDENEDIOXY)-3-HYDROXY-2,4,6-TRIMETHYLNONAN-8-OLID-7-YL-(E)-(R)-4-HYDROXY-2-OCTENOATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C6D6

View Spectrum of (2R,3S,4R,5R,6R,7S,8R)-4,5-(CYCLOHEXYLIDENEDIOXY)-3-HYDROXY-2,4,6-TRIMETHYLNONAN-8-OLID-7-YL-(E)-(R)-4-HYDROXY-2-OCTENOATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(2S,3R,4R,5R,6R,7S,8R)-3-(BENZYLOXYMETHOXY)-7-(TERT.-BUTYLDIMETHYLSILOXY)-4,5-(CYCLOHEXYLIDENEDIOXY)-8-HYDROXY-2,4,6-TRIMETHYLNONANOIC-ACID
3-BETA,4-BETA-EPOXY-1-BETA,2-BETA,8-TRIANGELOYLOXY-BISABOL-7-(14)-ENE
ARBORTRISTOSIDE-D
CAUDATOSIDE-B
7-O-TRANS-CINNAMOYL-7-BETA-HYDROXYLOGANIN
2',3'-DIACETYL-ISOVALEROSIDATE
1-[(Benzoyloxy)methyl]-6-[(4'-phenylbutanoyl)oxymethyl]-7-oxabicyclo[2.2.1]heptane-2,3-dicarboxylic Anhydride
SESQUITERPENE FC-XI
SESQUITERPENE FC-X
DURUMHEMIKETALOLIDE_B;(1-R*,3-R*,4-S*,14-S*,7-E,11-E)-18-ACETOXY-14-HYDROXY-4,14-EPOXYCEMBRA-7,11,15-(17)-TRIEN-16,3-OLIDE
Title Journal or Book Year
Stereoselective Total Synthesis of the Proposed Structure of 2-Epibotcinolide Organic Letters 2006

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