Cross-coupling of hydroxycinnamyl aldehydes into lignins

Organic Letters

Volumn 2, Issue 15, 2000, Pages 2197-2200

  Kim, Hoon ^a,b   Ralph, John ^a,b   Yahiaoui, Nabila ^c   Pean, Michel ^d   Boudet, Alain M ^c  

^a U S DAIRY FORAGE RESEARCH CENTER   (United States)

^b UNIVERSITY OF WISCONSIN MADISON   (United States)

^c Lab Biologie Molec Rel Plantes M   (France)

^d IRFM   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL DEHYDROGENASE; ALDEHYDE; CINNAMIC ACID DERIVATIVE; CINNAMYL ALCOHOL DEHYDROGENASE; DRUG DERIVATIVE; GUAIACOL; LIGNIN; P HYDROXYCINNAMALDEHYDE; P-HYDROXYCINNAMALDEHYDE;

ARTICLE; BIOSYNTHESIS; CHEMISTRY; ENZYMOLOGY; GENETICS; METABOLISM; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; TRANSGENIC PLANT;

ALCOHOL OXIDOREDUCTASES; ALDEHYDES; CINNAMATES; GUAIACOL; LIGNIN; MAGNETIC RESONANCE SPECTROSCOPY; PLANTS, GENETICALLY MODIFIED;

EID: 0034720943     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol005906o     Document Type: Article

References (42)

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32. 1H-broadband} probe equipped with 3-axis gradients. The long-range coupling delay was 80 ms.
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40. There is some suggestion in spectra from guaiacyl-only lignins and synthetic lignins (not shown) that coniferyl aldehyde may cross-couple with other 5-substituted guaiacyl units.
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