Compounds > 1-1-diphenyl-2-picrylhydrazyl

1-1-diphenyl-2-picrylhydrazyl and hydroxymatairesinol

1-1-diphenyl-2-picrylhydrazyl has been researched along with hydroxymatairesinol* in 1 studies

Other Studies

1 other study(ies) available for 1-1-diphenyl-2-picrylhydrazyl and hydroxymatairesinol

Article	Year
Derivatives of the Lignan 7'-Hydroxymatairesinol with Antioxidant Properties and Enhanced Lipophilicity. Journal of natural products, 2017, 06-23, Volume: 80, Issue:6 The lignan 7'-hydroxymatairesinol (1), extracted from the knotwoods of fir (Abies alba), spruce (Picea abies), and Douglas fir (Pseudotsuga menziesii), exhibited unexpected reactivity when esterification reactions were attempted on the hydroxy group at position C-7'. To circumvent the rapid intramolecular cyclization procedure, leading quantitatively to the lignan conidendrin (7), a simple strategy for 7'-esterification of 1 under mild conditions (three steps, up to 80% overall yield) was developed. Compared to hydroxymatairesinol (1) (log K' Topics: alpha-Tocopherol; Antioxidants; Biphenyl Compounds; Lignans; Molecular Structure; Nuclear Magnetic Resonance, Biomolecular; Picea; Picrates; Pinus; Stereoisomerism; Tetrahydronaphthalenes	2017

Article

Year

Derivatives of the Lignan 7'-Hydroxymatairesinol with Antioxidant Properties and Enhanced Lipophilicity.

Journal of natural products, 2017, 06-23, Volume: 80, Issue:6

The lignan 7'-hydroxymatairesinol (1), extracted from the knotwoods of fir (Abies alba), spruce (Picea abies), and Douglas fir (Pseudotsuga menziesii), exhibited unexpected reactivity when esterification reactions were attempted on the hydroxy group at position C-7'. To circumvent the rapid intramolecular cyclization procedure, leading quantitatively to the lignan conidendrin (7), a simple strategy for 7'-esterification of 1 under mild conditions (three steps, up to 80% overall yield) was developed. Compared to hydroxymatairesinol (1) (log K'

Topics: alpha-Tocopherol; Antioxidants; Biphenyl Compounds; Lignans; Molecular Structure; Nuclear Magnetic Resonance, Biomolecular; Picea; Picrates; Pinus; Stereoisomerism; Tetrahydronaphthalenes

2017