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(2R*,6R*/6S*,2'S*,3'R*,7'R*)-6-PIVALOYLOXY-2-(3'-HYDROXY-3'-METHYL-7'-PENTYLOXEPAN-2'-YLMETHYL)-6H-PYRAN-3-ONE;MAJOR-ISOMER

Compound with spectra: 2 NMR

(2R*,6R*/6S*,2'S*,3'R*,7'R*)-6-PIVALOYLOXY-2-(3'-HYDROXY-3'-METHYL-7'-PENTYLOXEPAN-2'-YLMETHYL)-6H-PYRAN-3-ONE;MAJOR-ISOMER
SpectraBase Compound ID FdgRPJff7yW
InChI InChI=1S/C23H38O6/c1-6-7-8-10-16-11-9-14-23(5,26)19(27-16)15-18-17(24)12-13-20(28-18)29-21(25)22(2,3)4/h12-13,16,18-20,26H,6-11,14-15H2,1-5H3/t16-,18-,19+,20?,23-/m1/s1
InChIKey LIQHMCIFIIKWRI-FACUHDIBSA-N
Mol Weight 410.6 g/mol
Molecular Formula C23H38O6
Exact Mass 410.266839 g/mol
Enantiomer InChIKey LIQHMCIFIIKWRI-XHWHODNYSA-N

View Spectrum of (2R*,6R*/6S*,2'S*,3'R*,7'R*)-6-PIVALOYLOXY-2-(3'-HYDROXY-3'-METHYL-7'-PENTYLOXEPAN-2'-YLMETHYL)-6H-PYRAN-3-ONE;MAJOR-ISOMER

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*,6R*/6S*,2'S*,3'R*,7'R*)-6-PIVALOYLOXY-2-(3'-HYDROXY-3'-METHYL-7'-PENTYLOXEPAN-2'-YLMETHYL)-6H-PYRAN-3-ONE;MAJOR-ISOMER

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C6D6
  • (2R*,6R*/6S*,2'S*,3'R*,7'R*)-6-PIVALOYLOXY-2-(3'-HYDROXY-3'-METHYL-7'-PENTYLOXEPAN-2'-YLMETHYL)-6H-PYRAN-3-ONE;MINOR-ISOMER
(2R*,2'S*,3'S*,7'S*)-2-(2'-FURAN-2-YL-2'-TERT.-BUTYLDIMETHYLSILYLOXYETHYL)-3-METHYL-7-PENTYLOXEPAN-3-OL
CNIFNURAJJZMON-OPTANORISA-N
(+)-3-O-allyl-4-O-Benzyl-1,2:5,6-di-O-cyclohexylidene-myo-inositol
CULOBOPHYLIN-A
FYSTZQYZRWEQPY-AUGIDONXSA-N
Thromoboxane B2 methyl ester 9,11,15-triacetate
ZBSIRDQYGJSYOS-MKZMQRORSA-N
(+-)-(3aR,4S,6R,6aR)-6-Methoxy-3-methylene-4-octyltetrahydrofura[3,4-b]furan-2(3H)-one
(-)-4,5,6-Tri-O-allyl-1-O-(p-methoxybenzyl)-2,3-cyclohexylidene-myo-inositol
(2E,6S)-6-Acetoxy-6-[(2R,5R,6S)-5-ethyl-5-acetoxy-6-methyltetrahydropyran-2-yl]hept-2-en-1-ol
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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