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YPNHSXBOWJTVIS-JEZHCXPESA-N

Compound with spectra: 2 NMR

YPNHSXBOWJTVIS-JEZHCXPESA-N
SpectraBase Compound ID EyJvvG8E9aA
InChI InChI=1S/C11H16O2/c1-7-3-5-9-8(2)11(12)13-10(9)6-4-7/h7,9-10H,2-6H2,1H3/t7-,9+,10+/m1/s1
InChIKey YPNHSXBOWJTVIS-JEZHCXPESA-N
Mol Weight 180.25 g/mol
Molecular Formula C11H16O2
Exact Mass 180.11503 g/mol
Enantiomer InChIKey YPNHSXBOWJTVIS-FXBDTBDDSA-N

View Spectrum of YPNHSXBOWJTVIS-JEZHCXPESA-N

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

View Spectrum of YPNHSXBOWJTVIS-JEZHCXPESA-N

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (3A-ALPHA,8A-ALPHA)-6-ALPHA-METHYL-3-METHYLENEOCTAHYDRO-2H-CYCLOHEPTA-[B]-FURAN-2-ONE
YPNHSXBOWJTVIS-HGNGGELXSA-N
Methyl (2R,3R)-(4-Methylene-5-oxo-2-propyltetrahydrofuran-3-yl)acetate
(+)-Protolichesterinic Acid
Protolichesterinic acid
(+)-protopraesorediosic acid
MUROLIC-ACID
ALLO-MUROLIC-ACID
8-Methyl-4-methylen-2-oxabicyclo[4.4.0]decan-3-one
(2S,3R)-2-amyl-5-keto-4-methylene-tetrahydrofuran-3-carboxylic acid
2-Amyl-5-keto-4-methylene-tetrahydrofuran-3-carboxylic acid
Title Journal or Book Year
Synthetic Method and Biological Activities of cis-Fused α-Methylene γ-Lactones Journal of Natural Products 2003
A Novel Synthetic Method of the (±)-(3aα,8aα)-Ethyl 8β-Hydroxy-6β-methyl-2-oxooctahydro-2H-cyclohepta[b]furan-3α- carboxylate and Its Chemical Transformation to (±)-(3aα,8aα)-3α,6β-Dimethyl-3,3a,4,5,6,8a-hexahydro-2H- cyclohepta[b]furan-2-one, (+)- and (−)-7β-(2-Acetoxy-1α-methylethyl)-4β-methyl-2-cyclohepten-1β-ol, and (+)- and (−)-7β-(2-Acetoxy-1α-methylethyl)-4β-methyl-2-cyclohepten-1-one. Possible Common Synthetic Intermediates for Pseudoguaianolides, 4,5-Secopseudoguaianolides, Guaianolides, 4,5-Secoguaianolides, and Octalactins The Journal of Organic Chemistry 1998

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