lignans and maleic-acid

lignans has been researched along with maleic-acid* in 1 studies

Other Studies

1 other study(ies) available for lignans and maleic-acid

Article	Year
A convenient route to the synthesis of isotopomeric dihydro-2(3H)furanones. Journal of agricultural and food chemistry, 2007, May-16, Volume: 55, Issue:10 A general synthetic procedure leading to isotopomeric dihydro-2(3H)furanones (gamma-butyrolactones) containing two, four, or six deuterium atoms has been developed. The labeled dihydro-2(3H)furanones were synthesized in quantitative yield from the saturated diacid C4 (succinic) or unsaturated diacids C4 (fumaric, maleic, or acetylendicarboxylic) in the presence of Ru4H4(CO)8(PBu3)4 using a deuterium pressure of 180 bar at 180 degrees C. This methodology was applied to the total synthesis of a hexadeuterated matairesinol lignan: The 3,4-bis[[3-methoxy-4-(phenylmethoxy)phenyl]methyl]dihydro-2(3H)furanone-[7,7',8,8',9',9'-D6] (benzyl-protected matairesinol-D6) was fully characterized. Topics: 4-Butyrolactone; Deuterium; Fumarates; Furans; Isotope Labeling; Lignans; Maleates; Ruthenium; Succinic Acid	2007

Article

Year

A convenient route to the synthesis of isotopomeric dihydro-2(3H)furanones.

Journal of agricultural and food chemistry, 2007, May-16, Volume: 55, Issue:10

A general synthetic procedure leading to isotopomeric dihydro-2(3H)furanones (gamma-butyrolactones) containing two, four, or six deuterium atoms has been developed. The labeled dihydro-2(3H)furanones were synthesized in quantitative yield from the saturated diacid C4 (succinic) or unsaturated diacids C4 (fumaric, maleic, or acetylendicarboxylic) in the presence of Ru4H4(CO)8(PBu3)4 using a deuterium pressure of 180 bar at 180 degrees C. This methodology was applied to the total synthesis of a hexadeuterated matairesinol lignan: The 3,4-bis[[3-methoxy-4-(phenylmethoxy)phenyl]methyl]dihydro-2(3H)furanone-[7,7',8,8',9',9'-D6] (benzyl-protected matairesinol-D6) was fully characterized.

Topics: 4-Butyrolactone; Deuterium; Fumarates; Furans; Isotope Labeling; Lignans; Maleates; Ruthenium; Succinic Acid

2007