lignans and piperonal

lignans has been researched along with piperonal* in 2 studies

Other Studies

2 other study(ies) available for lignans and piperonal

Article	Year
Antioxidant properties of 8.0.4'-neolignans. Phytomedicine : international journal of phytotherapy and phytopharmacology, 2001, Volume: 8, Issue:6 A series of naturally occurring 8.0.4'-neolignans (1a-d, 1g, 2g, 2h) and their analogues (le-f, lh, 1i, 2a-f, 2i) have been synthesized in racemic form starting from commercially available phenols, such as eugenol, isoeugenol and 4-allyl-2,6-dimethoxyphenol and from aromatic aldehydes, such as piperonal, veratraldehyde and 3,4,5-trimethoxybenzaldehyde. The inhibitory activity of these compounds on superoxide anion (O2.-) release by human polymorphonuclear leukocytes (PMNLs) was tested and the structure-activity relationship was also studied. Topics: Aldehydes; Antioxidants; Benzaldehydes; Benzodioxoles; Cells, Cultured; Eugenol; Humans; Lignans; Neutrophils; Phenols; Quantitative Structure-Activity Relationship; Superoxides	2001
Synthesis of optically active olivil type of lignan from L-arabinose using threo-selective aldol condensation as a key reaction. Bioscience, biotechnology, and biochemistry, 2000, Volume: 64, Issue:11 The threo-selective aldol condensation of (3R, 4S)-3-hydroxy-5-trityloxy-4-pentanolide, which was prepared from L-arabinose, with piperonal was applied to the stereoselective synthesis of the olivil type of lignan, (2R, 3R, 4R)-4-benzyl-4-hydroxy-3-hydroxymethyl-2-(3,4-methylenedioxyphenyl)tetrahydrofuran. Topics: Aldehydes; Arabinose; Benzaldehydes; Benzodioxoles; Lignans; Optical Rotation; Stereoisomerism	2000

Article

Year

Antioxidant properties of 8.0.4'-neolignans.

Phytomedicine : international journal of phytotherapy and phytopharmacology, 2001, Volume: 8, Issue:6

A series of naturally occurring 8.0.4'-neolignans (1a-d, 1g, 2g, 2h) and their analogues (le-f, lh, 1i, 2a-f, 2i) have been synthesized in racemic form starting from commercially available phenols, such as eugenol, isoeugenol and 4-allyl-2,6-dimethoxyphenol and from aromatic aldehydes, such as piperonal, veratraldehyde and 3,4,5-trimethoxybenzaldehyde. The inhibitory activity of these compounds on superoxide anion (O2.-) release by human polymorphonuclear leukocytes (PMNLs) was tested and the structure-activity relationship was also studied.

Topics: Aldehydes; Antioxidants; Benzaldehydes; Benzodioxoles; Cells, Cultured; Eugenol; Humans; Lignans; Neutrophils; Phenols; Quantitative Structure-Activity Relationship; Superoxides

2001

Synthesis of optically active olivil type of lignan from L-arabinose using threo-selective aldol condensation as a key reaction.

Bioscience, biotechnology, and biochemistry, 2000, Volume: 64, Issue:11

The threo-selective aldol condensation of (3R, 4S)-3-hydroxy-5-trityloxy-4-pentanolide, which was prepared from L-arabinose, with piperonal was applied to the stereoselective synthesis of the olivil type of lignan, (2R, 3R, 4R)-4-benzyl-4-hydroxy-3-hydroxymethyl-2-(3,4-methylenedioxyphenyl)tetrahydrofuran.

Topics: Aldehydes; Arabinose; Benzaldehydes; Benzodioxoles; Lignans; Optical Rotation; Stereoisomerism

2000