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(3-[5S-(2S,3S-EPOXY-5S-HYDROXY-4S-METHYLHEXYL)-3R,4R-DIHYDROXYTETRAHYDROPYRAN-2S-YL]-2-METHYLPROP-1(E)-EN-YL)-2-METHYLFUR-4-YL-KETONE

Compound with spectra: 1 NMR

(3-[5S-(2S,3S-EPOXY-5S-HYDROXY-4S-METHYLHEXYL)-3R,4R-DIHYDROXYTETRAHYDROPYRAN-2S-YL]-2-METHYLPROP-1(E)-EN-YL)-2-METHYLFUR-4-YL-KETONE
SpectraBase Compound ID GkTFmZRubRx
InChI InChI=1S/C22H32O7/c1-11(5-17(24)15-7-12(2)27-9-15)6-18-21(26)20(25)16(10-28-18)8-19-22(29-19)13(3)14(4)23/h5,7,9,13-14,16,18-23,25-26H,6,8,10H2,1-4H3/b11-5+/t13-,14-,16-,18-,19+,20+,21-,22-/m0/s1
InChIKey IQTCIZHRZCEBSV-LHHURDMNSA-N
Mol Weight 408.5 g/mol
Molecular Formula C22H32O7
Exact Mass 408.214803 g/mol
Enantiomer InChIKey IQTCIZHRZCEBSV-KCVCAOIYSA-N

View Spectrum of (3-[5S-(2S,3S-EPOXY-5S-HYDROXY-4S-METHYLHEXYL)-3R,4R-DIHYDROXYTETRAHYDROPYRAN-2S-YL]-2-METHYLPROP-1(E)-EN-YL)-2-METHYLFUR-4-YL-KETONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD
N'-Benzoyl-monohydrazide
Benzoic acid, 2-[3-methyl-1-oxo-4-[tetrahydro-3,4-dihydroxy-5-[[3-(2-hydroxy-1-methylpropyl)oxiranyl]methyl]-2H-pyran-2-yl]-2-butenyl]hydrazide, [2S-[2.alpha.(E),3.beta.,4.beta.,5.alpha.[2R*,3R*(1R*,2R*)]]]-
N-Normonyl-N-(p-Nitrophenyl)momohydrazide
N'-(p-NITROPHENYL)-MONOHYDRAZIDE
Benzamide O-monyl oxime
Phenacyl-monamide
2-Butenamide, 3-methyl-N-(2-oxo-2-phenylethyl)-4-[tetrahydro-3,4-dihydroxy-5-[[3-(2-hydroxy-1-methylpropyl)oxiranyl]methyl]-2H-pyran-2-yl]-, [2S-[2.alpha.(E),3.beta.,4.beta.,5.alpha.[2R*,3R*(1R*,2R*)]]]-
N-Normonyl-N-(pyridylmethyl)monoamide N-{(1E)-[5-(2S,3S,4S,5S)-(2,3-Epoxy-5-hydroxy-4-methylhexyl)-(2S,3R,4R,5S)-3,4-dihydroxytetrahydropyran-2-yl]-2-methylprop-1-en-1-yl}-N-(pyridylmethyl)amide
N-PYRIDYL-METHYL-MONOAMIDE
N-[2-(1,3-Dithian-2-yl)2-oxoethyl])monamide
Title Journal or Book Year
Chemistry of Pseudomonic Acid. Part 16. Aryl and Heteroaryl Ketone Derivatives of Monic Acid. The Journal of Antibiotics 1996
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