Determination of the geometry of acetoxyendiynes and acetoxyenynes by NMR heteronuclear 13C-1H scalar couplings and 13C NMR chemical shifts. Structural assignment of the oxylipin natural products peyssonenynes A and B

Magnetic Resonance in Chemistry

Volumn 48, Issue 7, 2010, Pages 543-549

  García, Patricia ^a   Martín Pastor, Manuel ^b   De Lera, Ángel R ^a   Álvarez, Rosana ^a  

^a UNIVERSITY OF VIGO   (Spain)

^b UNIVERSITY OF SANTIAGO DE COMPOSTELA   (Spain)

Author keywords

Acetoxyendiynes; Acetoxyenynes; EXSIDE; H C long range couplings; Heteronuclear scalar couplings

Indexed keywords

CHEMICAL BONDS; CHEMICAL SHIFT; COUPLINGS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; OLEFINS; PALMITIC ACID;

ACETOXYENDIYNES; ACETOXYENYNES; DETECTION EXPERIMENTS; DOUBLE BONDS; EXCITATION SCULPTURED INDIRECT DETECTION EXPERIMENT; H-C LONG RANGE COUPLING; HETERONUCLEAR; HETERONUCLEAR SCALAR COUPLING; INDIRECT DETECTION; SCALAR COUPLING;

GEOMETRY;

BIOLOGICAL PRODUCT; CARBON; ENEDIYNE; OXYLIPIN; PEYSSONENYNE A; PEYSSONENYNE B; PROTON; UNSATURATED FATTY ACID;

CHEMICAL STRUCTURE; CHEMISTRY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; ISOLATION AND PURIFICATION; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PROCEDURES; RED ALGA; STEREOISOMERISM;

BIOLOGICAL PRODUCTS; CARBON ISOTOPES; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; ENEDIYNES; FATTY ACIDS, UNSATURATED; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR STRUCTURE; OXYLIPINS; PROTONS; RHODOPHYTA; STEREOISOMERISM;

EID: 77953928661     PISSN: 07491581     EISSN: 1097458X     Source Type: Journal    
DOI: 10.1002/mrc.2618     Document Type: Article

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