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[R-(R*,R*S*),5-ALPHA]-4-(5,6-DIHYDRO-5-HYDROXY-2-H-PYRAN-2-YL)-3-METHYL-2-BUTANONE

Compound with spectra: 1 NMR

[R-(R*,R*S*),5-ALPHA]-4-(5,6-DIHYDRO-5-HYDROXY-2-H-PYRAN-2-YL)-3-METHYL-2-BUTANONE
SpectraBase Compound ID QgQZoaWo59
InChI InChI=1S/2C10H16O3/c2*1-7(8(2)11)5-10-4-3-9(12)6-13-10/h2*3-4,7,9-10,12H,5-6H2,1-2H3/t2*7-,9-,10-/m10/s1
InChIKey XAWKLRYSYVVZKT-FSKDWHSISA-N
Mol Weight 368.47 g/mol
Molecular Formula C20H32O6
Exact Mass 368.219889 g/mol
Enantiomer InChIKey XAWKLRYSYVVZKT-CPPBOAPYSA-N

View Spectrum of [R-(R*,R*S*),5-ALPHA]-4-(5,6-DIHYDRO-5-HYDROXY-2-H-PYRAN-2-YL)-3-METHYL-2-BUTANONE

13C NMR Spectrum
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Solvent CDCl3
6-METHYL-5-(10-OXYMETHYLENE-ISOBUTYLENE)-LACTONE
trans-((E)-3-Acetoxy-3-methyl-1-buten-1-yl)-4-methyltetrahydrofuran
cis-2-((E)-3-Acetoxy-3-methyl-1-buten-1-yl)-4-methyltetrahydrofuran
3-((tetrahydrofuran-2-yl)methyl)octan-2-one
trans-1-Acetoxy-4-iso-butoxy-2-cyclohexene
syn-2-(Cyclohexyl)-6-methyloxacyclohex-3-ene
(+)-cis-4-Pivaloyloxycyclohex-2-enol
Deacetyl-umuravumbolide
(-)-TRANS-7E-ROSE_OXIDE-8-CARBOXYLIC_ACID
(-)-CIS-7E-ROSE_OXIDE-8-CARBOXYLIC_ACID
Title Journal or Book Year
Stereocontrolled routes to functionalized [1,8-bc]naphthopyran. A study on the total synthesis of quassinoids and tetrahydronaphthalene antibiotics The Journal of Organic Chemistry 1993
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