Formation of optically active neolignans from achiral coniferyl alcohol by cell-free extracts of Eucommia ulmoides
Open Access
- 1 June 1998
- journal article
- Published by Springer Nature in Journal of Wood Science
- Vol. 44 (3), 244-246
- https://doi.org/10.1007/bf00521971
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Stereoselective Bimolecular Phenoxy Radical Coupling by an Auxiliary (Dirigent) Protein Without an Active CenterScience, 1997
- (+)-Pinoresinol synthase: A stereoselective oxidase catalysing 8,8′-lignan formation in Forsythia intermediaTetrahedron Letters, 1994
- Absolute Configuration of Dehydrodiconiferyl AlcoholBioscience, Biotechnology, and Biochemistry, 1994
- An extraordinary accumulation of (−)-pinoresinol in cell-free extracts of Forsythia intermedia: evidence for enantiospecific reduction of (+)-pinoresinolPhytochemistry, 1992
- On the stereoselective synthesis of (+)-pinoresinol in Forsythia suspensa from its achiral precursor, coniferyl alcoholPhytochemistry, 1992
- Biosynthesis of Dehydrodiconiferyl Alcohol Glucosides: Implications for the Control of Tobacco Cell GrowthPlant Physiology, 1992
- The constituents of Eucommia ulmoides Oliv. VI. Isolation of a new sesquilignan and neolignan glycosides.CHEMICAL & PHARMACEUTICAL BULLETIN, 1987
- The constituents of Eucommia ulmoides Oliv. V. Isolation of dihydroxydehydrodiconiferyl alcohol isomers and phenolic compounds.CHEMICAL & PHARMACEUTICAL BULLETIN, 1987