For citations & permissions, please see: Citations & Permissions - Wiley Science Solutions*

*Links on SpectraBase are not permalinks.

[2R-(2-ALPHA-(R*,S*),6-BETA)]-4-(6-[(ACETYLOXY)-METHYL]-3,6-DIHYDRO-3-OXO-2H-PYRAN-2-YL)-3-METHYL-2-BUTANONE,ISOMER-#1

Compound with spectra: 2 NMR

[2R-(2-ALPHA-(R*,S*),6-BETA)]-4-(6-[(ACETYLOXY)-METHYL]-3,6-DIHYDRO-3-OXO-2H-PYRAN-2-YL)-3-METHYL-2-BUTANONE,ISOMER-#1
SpectraBase Compound ID IDiJa0MSnWb
InChI InChI=1S/C13H18O5/c1-8(9(2)14)6-13-12(16)5-4-11(18-13)7-17-10(3)15/h4-5,8,11,13H,6-7H2,1-3H3/t8?,11-,13+/m1/s1
InChIKey NHPXLXWJBXPISJ-KQBUEYNVSA-N
Mol Weight 254.28 g/mol
Molecular Formula C13H18O5
Exact Mass 254.115424 g/mol
Enantiomer InChIKey NHPXLXWJBXPISJ-XIWYHIBGSA-N

View Spectrum of [2R-(2-ALPHA-(R*,S*),6-BETA)]-4-(6-[(ACETYLOXY)-METHYL]-3,6-DIHYDRO-3-OXO-2H-PYRAN-2-YL)-3-METHYL-2-BUTANONE,ISOMER-#1

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of [2R-(2-ALPHA-(R*,S*),6-BETA)]-4-(6-[(ACETYLOXY)-METHYL]-3,6-DIHYDRO-3-OXO-2H-PYRAN-2-YL)-3-METHYL-2-BUTANONE,ISOMER-#1

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • [2R-(2-ALPHA-(R*,S*),6-BETA)]-4-(6-[(ACETYLOXY)-METHYL]-3,6-DIHYDRO-3-OXO-2H-PYRAN-2-YL)-3-METHYL-2-BUTANONE,ISOMER-#2
1-(4-Acetoxy-2-chloro-2-methyl)-butyl C-1,2,3,4-tetradeoxy-L-rhamno-hex-3-en-2-ono-pyranoside
[(2S,5S,6R)-5-Methyl-6-[3-(triisopropylsilyloxy)propyl]-5,6-dihydro-2H-pyran-2-ylmethyl ester]-2,2-dimethylpropionic acid
DIPLOBIFURANYLONE_A;5'-[(1-S)-1-HYDROXYETHYL]-3,4-2',5'-TETRAHYDRO-2-H-[2.2']-BIFURANYL-5-ONE
DIPLOBIFURANYLONE_B;5'-[(1-R)-1-HYDROXYETHYL]-3,4-2',5'-TETRAHYDRO-2-H-[2.2']-BIFURANYL-5-ONE
2-[5'-(1"-Hydroxyethyl)-2',5'-dihydrofuran-2'-yl]-2,3,4,5-tetrafuran-5-one
Ethyl 5-butyl-5-hexyl-2,5-dihydrofurancarboxylate
(2S,3S,5R)-5-((E)-4-Benzoyloxy-but-1-enyl)-3-hydroxy-tetrahydro-furan-2-carboxylic acid methyl ester
(2S,3S,5S)-5-((E)-4-Benzoyloxy-but-1-enyl)-3-hydroxy-tetrahydro-furan-2-carboxylic acid methyl ester
(E)-(S)-4-((2R,3S)-2-Allyl-tetrahydro-pyran-3-yloxy)-5-(tert-butyl-dimethyl-silanyloxy)-pent-2-enal
rel-(2R,3S,6R)-6-methyl-2-carbomethoxy-3-propenylterahydropyran
Title Journal or Book Year
Lewis acid induced homoallylic C-alkylation. 2. Application to the synthesis of unsaturated diketo C-glycosides. Mechanistic aspect of the reaction The Journal of Organic Chemistry 1992
Other Resources
Unknown Identification

Search your unknown spectrum against the world's largest collection of reference spectra

KnowItAll Campus Solutions

KnowItAll offers faculty and students at your school access to all the tools you need for spectral analysis and structure drawing & publishing! Plus, access the world's largest spectral library.