3-(4-Hydroxyphenyl)propionic acid is involved in the biosynthesis of myricanol in Myrica rubra

There is little evidence concerning the biosynthetic pathways for cyclic diarylheptanoids. We previously demonstrated that the cyclic diarylheptanoids myricanol and myricanone were biologically synthesized from two molecules of 4-coumaric acid by the feeding of 4-[8,9-¹³C₂]coumaric acid to young shoots of Myrica rubra. In the present study, using a ¹³C-labeled compound, we revealed that two molecules of 3-(4-hydroxyphenyl)propionic acid could also be a biosynthetic precursor of myricanol in M. rubra. These results indicated that both 4-coumaric acid and its dihydro-derivative were incorporated into myricanol. Competitive feeding experiments with 4-[8,9-¹³C₂]coumaric acid and 3-(4-hydroxyphenyl)-[1-¹³C]propionic acid were performed in M. rubra to determine the preferential incorporation of these two precursors. ¹³C-NMR studies indicated that 3-(4-hydroxyphenyl)-[1-¹³C]propionic acid was preferentially incorporated into myricanol. The data provided evidence for a biosynthetic sequence originating from 4-coumaric acid and leading to myricanol, through 3-(4-hydroxyphenyl)propionic acid, in M. rubra.     

Stereochemistry and biosynthesis of 8-O-4′ neolignans in Eucommia ulmoides: diastereoselective formation of guaiacylglycerol-8-O-4′-(sinapyl alcohol) ether

Stereochemistry and biosynthesis of guaiacylglycerol-8-O-4′-(sinapyl alcohol) ether (GGSE), an 8-O-4′ neolignan, which consists of coniferyl and sinapyl alcohol moieties, in Eucommia ulmoides were investigated. Four 8-O-4′ neolignans, GGSE, syringylglycerol-8-O-4′-(coniferyl alcohol) ether (SGCE), guaiacylglycerol-8-O-4′-(coniferyl alcohol) ether (GGCE), and syringylglycerol-8-O-4′-(sinapyl alcohol) ether (SGSE), were synthesized. Their erythro and threo diastereomers were separated through acetonide derivatives, intermediates of the synthesis, and identified by means of nuclear magnetic resonance (NMR) spectroscopy. All of the erythro-acetonide derivatives have larger coupling constants (ca 9 Hz) for the C₇-H resonances than those of the threo ones (1.5–2 Hz). In the case of the four 8-O-4′ neolignans, the C₇-H coupling constants of the threo-isomers are not smaller than those of the erythro ones. GGSE isolated previously from this plant was identified as the erythro isomer by comparison of the ¹³C-NMR data with synthetic erythro-GGSE and threo-GGSE and the other 8-O-4′ neolignans mentioned as above. Administration of a mixture of [8-¹⁴C]coniferyl alcohol and [8-¹⁴C]sinapyl alcohol to excised shoots of E. ulmoides was carried out and the incorporation of ¹⁴C into erythro-[¹⁴C]GGSE was found to be higher than that in threo-[¹⁴C]GGSE. The occurrence of diastereoselective formation of erythro-GGSE by cross coupling of coniferyl and sinapyl alcohols is suggested.Part of this paper was presented at the 47th Lignin Symposium, Fukuoka, October 2002 and the 53rd Annual Meeting of the Japan Wood Research Society, Fukuoka, April 2003     

Cyclisation of farnesyl pyrophosphate into sesquiterpenoids in ginger rhizomes (Zingiber officinale)

The atomic ratios (¹⁴C/³H) obtained in ar-curcumene, α-zingiberene, β-bisabolene obtained from the essential oil of rhizomes of Zingiber officinale which were fed with [2-¹⁴C, 2-³H₂], [2-¹⁴C, 4R-³H₁] and [2-¹⁴C, 5-³H₂]mevalonic acid and [1-³H₂]farnesylpyrophosphate (FPP) revealed that (a) (2E,6E)-isomer of FPP is isomerised to (2Z,6E)-isomer without loss of epimeric hydrogen that means without a redox process; (b) (2Z,6E)-FPP is cyclised to bisabolyl cation which is the penultimate precursor of α-zingiberene, ar-curcumene and β-bisabolene; and (c) two 1,2-hydrogen shifts take place during the formation of α-zingiberene whereas one 1,2 shift has been observed during the formation of ar-curcumene.     

Effects of enhanced ultraviolet-B radiation on water use efficiency, stomatal conductance, leaf nitrogen content and morphological characteristics of Spiraea pubescens in a warm-temperate deciduous broad-leaved forest

Spiraea pubescens, a common shrub in the warm-temperate deciduous forest zone which is distributed in the Dongling Mountain area of Beijing, was exposed to ambient and enhanced ultraviolet-B (UV-B, 280–320 nm) radiation by artificially supplying a daily dose of 9.4 kJ/m² for three growing seasons, a level that simulated a 17% depletion in stratospheric ozone. The objective of this study was to explore the effects of long-term UV-B enhancement on stomatal conductance, leaf tissue δ ¹³C, leaf water content, and leaf area. Particular attention was paid to the effects of UV-B radiation on water use efficiency (WUE) and leaf total nitrogen content. Enhanced UV-B radiation significantly reduced leaf area (50.1%) but increased leaf total nitrogen content (102%). These changes were associated with a decrease in stomatal conductance (16.1%) and intercellular CO₂ concentration/ air CO₂ concentration (C _i /C _a) (4.0%), and an increase in leaf tissue δ ¹³C (20.5‰), leaf water content (3.1%), specific leaf weight (SLW) (5.2%) and WUE (4.1%). The effects of UV-B on the plant were greatly affected by the water content of the deep soil (30–40 cm). During the dry season, differences in the stomatal conductance, δ ¹³C, and WUE between the control and UV-B treated shrubs were very small; whereas, differences became much greater when soil water stress disappeared. Furthermore, the effects of UV-B became much less significant as the treatment period progressed over the three growing seasons. Correlation analysis showed that enhanced UV-B radiation decreased the strength of the correlation between soil water content and leaf water content, δ ¹³C, C _i/C _a, stomatal conductance, with the exception of WUE that had a significant correlation coefficient with soil water content. These results suggest that WUE would become more sensitive to soil water variation due to UV-B radiation. Based on this experiment, it was found that enhanced UV-B radiation had much more significant effects on morphological traits and growth of S. pubescens than hydro-physiological characteristics. __________ Translated from Journal of Plant Ecology, 2006, 30(1): 47–56 [译自: 植物生态学报]     

Stereochemistry and biosynthesis of (+)-lyoniresinol,a syringyl tetrahydronaphthalene lignan in <Emphasis Type="Italic">Lyonia ovalifolia</Emphasis> var. <Emphasis Type="Italic">elliptica</Emphasis> II: feeding experiments with <Superscript>14</Superscript>C labeled precursors

To clarify the biosynthetic pathway for syringyl lignans, especially syringyl tetrahydronaphthalene lignans and formation of the C2–C7′ linkage, production of (+)-lyoniresinol (LYR) and its predicted intermediates [syringaresinol (SYR), 5,5′-dimethoxylariciresinol (DMLR), and 5,5′-dimethoxysecoisolariciresinol (DMSLR)] in Lyonia ovalifolia var. elliptica was investigated by means of feeding experiments with radiolabeled precursors. Following individual administration of l-[U-¹⁴C]phenylalanine (Phe), [8-¹⁴C]sinapyl alcohol (SA), and [8,8′-¹⁴C]SYR to excised young shoots of L. ovalifolia and their subsequent metabolism, free [¹⁴C]lignans and [¹⁴C]lignan glycosides were extracted with methanol from stems and leaves and were divided into ethyl acetate-soluble fractions (lignans) and aqueous fractions (lignan glycosides), respectively. Using a combination of xylanase, cellulase, and β-glucosidase, the glycosides were hydrolyzed to liberate [¹⁴C]lignans as aglycones. l-[U-¹⁴C]Phe was incorporated into (+)-[¹⁴C]SYR [stem 0.38%, 8% enantiomeric excess (e.e.)], (−)-[¹⁴C]SYR (leaves 2.75%, 72% e.e.), (+)-[¹⁴C]DMLR (stem 0.07%, 18% e.e. and leaves 0.009%, 58% e.e.), (−)-[¹⁴C]DMSLR (stem 0.03%, 46% e.e. and leaves 0.05%, 20% e.e.), (+)-[¹⁴C]LYR (leaves 0.013%, 22% e.e.) and glycosides of (+)-[¹⁴C]LYR (stem 0.036%, 50% e.e.) in 24h. Based on the percent incorporation and enantiomeric composition of the lignans, the biosynthetic pathway of (8R,8′R)-(+)-LYR was proposed as follows: a nonselective dehydrogenative dimerization of sinapyl alcohol yields (±)-SYR, which is reduced with low specificity to give (8R,8′R)-(+)-DMLR. This is cyclized to directly give (+)-LYR as well as reduced again to (8R,8′R)-(−)-DMSLR. Although further transformation of (−)-DMSLR also leads to the formation of (+)-LYR, cyclization could be a main pathway for (+)-LYR biosynthesis. This report was presented at the IAWPS 2005 International Symposium on Wood Science and Technology, Yokohama, November 2005     

广州市酸雨对不同森林冠层淋溶规律的研究

１９９８年４月至１９９９年３月对广州市白云山马尾松林和常绿阔叶林、广州市龙眼洞马尾松林两试验点进行了酸雨的监测,并测定和分析了林内穿透雨物理量及化学量,旨在探讨酸雨对不同森林冠层养分淋溶规律的影响。结果表明：（１）广州市酸雨占次数的７９．７％或占降雨量的９５．１％。（２）酸雨通过林冠层后,ｐＨ值明显增加。（３）在马尾松林和常绿阔叶林中,某些单次降雨出现ＳＯ４＾２－、ＮＯ３＾－、ＮＨ４＾＋Ａｌ＾３＋、Ｎａ＾＋的负淋溶现象,说明森林对这些离子（特别是ＮＯ３＾－、Ａａ＾３＋）具有吸收作用;阔叶林全年的ＮＯ３＾－和Ａｌ＾３＋净淋溶为负值,说明阔叶林比马尾松林对这两种离子具有更强的吸收能力。（４）雨水酸度增加（即ｐＨ值减小）,明显提高阳离子Ｃａ＾２＋、Ｍｇ＾２＋、Ｋ＾＋和Ｎａ＾＋冠层淋溶面分率。（５）ＮＨ４＾＋、ＳＯ４＾     

Effects of young agroforestry trees on soils in on-farm situations in western Kenya

Soil samples were taken at different distances from the trunks of four- to five-year-old trees of six species planted on-farm in western Kenya. The tree species wereCordia africana, Croton megalocarpoides, Grevillea robusta, Acacia tortilis, Prosopis juliflora andSesbania sesban. Samples were also taken inside and outside a fenced plantation ofProsopis juliflora. Soil samples were analysed for total C%, total N%,¹³C abundance,¹⁵N abundance, extractable P and pH.The most sensitive indicator of effects of trees on soils was¹³C abundance, which reflected a shift in inputs of C from C₄ grasses to C from C₃ trees. All species except Prosopis lowered the¹³C abundance by 0.5–1 -units. This was equivalent to an increase of 3–5% of the percentage of C contributed by C₃ species. Prosopis trees did not decrease the¹³C abundance because of the abundant grass-growth around them. Cordia, which had the most pronounced effects, raised the C%, N% and extractable P by 27%, 26% and 55%, respectively. Nitrogen and C were well correlated (r ²=0.97) in the whole material. Effects on soil pH were in both directions, i.e. it was raised under the Prosopis plantation by 0.33 units, while it was lowered under Acacia by 0.21 units.Effects of agroforestry trees were thus seen in as short time as five years in practical onfarm situations.¹³C abundance is recommended as a particularly sensitive indicator of the influence of trees on sites previously dominated by C₄ crops and grasses.     

Analysis of the structure of lignin-carbohydrate complexes by the specific13C tracer method

In the present study the specifically¹³C-enriched lignin precursors of biosynthesis (i.e., coniferin-[side chain–¹³C], coniferin-[side chain-–¹³C] and coniferin-[side chain-–¹³C]) were synthesized and administered exogeneously to ginkgo shoots (Ginkgo biloba L.) to obtain¹³C-enriched lignin-carbohydrate complexes (LCCs). The specifically¹³C-enriched LCCs were isolated from the newly formed xylem of ginkgo shoots administered with the¹³C-enriched precursors and degraded by enzymes. Lignin-rich fractions, so called enzyme-degraded LCCs (EDLCCs), were obtained. By determining their¹³C-NMR spectra, information related to the chemical structure of lignin building units and linkages between phenylpropane units of lignin and carbohydrates were obtained. It was found that these precursors were incorporated in natural lignin successfully. Three lignin-carbohydrates linkages (i.e., ether type, ester type, ketal type) were found at the C -position of the side chain of phenylpropane units in ginkgo LCC. No lignin-carbohydrate bond at the C- or C-position of the lignin side chain was observed in the¹³C-NMR spectra of the¹³C-enriched LCCs. This fact indicates that a specific¹³C tracer technique can be useful in NMR study of the chemical structure of LCCs.Part of this paper was presented at the 5th Pacific Polymer Conference, Kyongju, Korea, October 1997     

Biosynthesis of a syringyl 8-O-4′ neolignan in Eucommia ulmoides: formation of syringylglycerol-8-O-4′-(sinapyl alcohol) ether from sinapyl alcohol

To investigate the biosynthesis and stereochemistry of syringylglycerol-8-O-4′-(sinapyl alcohol) ether (SGSE), a syringyl 8-O-4′ neolignan, feeding experiments and enzyme assays using Eucommia ulmoides were carried out. Diastereoselective formation of erythro-SGSE was found. When [8-¹⁴C]sinapyl alcohol was administered to excised shoots of E. ulmoides, ¹⁴C was incorporated into free SGSE and SGSE glucosides. In stems, incorporation into (+)-erythro-[¹⁴C]SGSE (0.037%) with 9.1% enantiomeric excess (% e.e.) was found; incorporation into the threo isomer was not detectable. Erythro-[¹⁴C]SGSE glucosides (0.047%) dominated over threo forms (0.007%) with 74.0% diastereomeric excess (% d.e.); both diastereomers were levorotatory with 32.0% e.e. and 18.3% e.e., respectively. In leaves, higher incorporation into (−)-erythro-[¹⁴C]SGSE (0.500%, 15.9% e.e.) than into the threo isomer (0.206%, 7.4% e.e.) was observed (41.6% d.e.). (−)-Erythro-[¹⁴C]SGSE glucosides (1.692%, 25.0% e.e.) were produced at higher rates than threo isomers (0.177%, 16.4% e.e.) with 81.0% d.e. In incubations of a mixture of [8-¹⁴C]sinapyl and [8-¹⁴C]coniferyl alcohols with an insoluble enzyme preparation from stems of E. ulmoides, erythro-SGSE was preferentially produced. The highest % d.e. (82.8) was observed at 60 min with the (+)-erythro isomer (21.4% e.e.) and the (−)-threo form (4.3% e.e.).Part of this report was presented at the 52nd Annual Meeting of the Japan Wood Research Society, Gifu, April 2002, and the 47th Lignin Symposium, Fukuoka, October 2002     

Foliar Carbon Isotope Composition (δ 13C) and Water Use Efficiency of Different Populus deltoids Clones Under Water Stress

Foliar carbon isotope composition (δ ¹³C), total dry biomass, and long-term water use efficiency (WUE_L) of 12 Populus deltoids clones were studied under water stress in a greenhouse. Total dry biomass of clones decreased greatly, while δ ¹³C increased. Single-element variance analysis in the same water treatment indicated that WUE_L difference among clones was significant. Clones J₂, J₆, J₇, J₈, and J₉ were excellent with high WUE_L. Extremely significant δ ¹³C differences among water treatments and clones were revealed by two-element variance analysis. Water proved to be the primary factor affecting δ ¹³C under water stress. It showed that there was a good positive correlation between δ ¹³C and WUE_L in the same water treatment, and that a high WUE_L always coincided with a high δ ¹³C. δ ¹³C might be a reliable indirect index to estimate WUE_L among P. deltoids clones. Translated from Scientia Silvae Sinicae, 2005, 41(1) (in Chinese)     

Dihydroroseoside, a new cyclohexanone glucoside, from the leaves of shirakamba (Betula platyphylla Sukatchev var.japonica Hara)

A new cyclohexanone glucoside (II) and a known cyclohexenone glucoside roseoside [I, (6S, 9S)-6-hydroxy-6-(9--D-glucopyranosyloxy-trans-7-butenyl)-1,5,5-trimethyl-1-cyclohexenone] were isolated from an ethanol extract of shirakamba (Betula platyphylla Sukatchev var.japonica Hara) leaves. The structure ofII was determined to be (6S, 9R)-6-hydroxy-6-(9-O--D-glucopyranosyloxy-trans-7-butenyl)-1, 5,5-trimethyl-1-cyclohexanone by¹H-NMR and¹³C-NMR spectroscopic analyses. It was named dihydroroseoside.     

Nitrogen-fixation dynamics in a cut-and-carry silvopastoral system in the subhumid conditions of Guadeloupe, French Antilles

This paper summarizes several studies on N recycling in a tropical silvopastoral system for assessing the ability of the system to increase soil fertility and insure sustainability. We analyzed the N₂ fixation pattern of the woody legume component (Gliricidia sepium), estimated the recycling rate of the fixed N in the soil, and measured N outputs in tree pruning and cut grass (Dichanthium aristatum). With this information, we estimated the N balance of the silvopastoral system at the plot scale. The studies were conducted in an 11-year-old silvopastoral plot established by planting G. sepium cuttings at 0.3 m × 2 m spacing in natural grassland. The plot was managed as a cut-and-carry system where all the tree pruning residues (every 2-4 months) and cut grass (every 40-50 days) were removed and animals were excluded. No N fertilizer was applied. Dinitrogen fixation, as estimated by the ¹⁵N natural abundance method, ranged from 60-90% of the total N in aboveground tree biomass depending on season. On average, 76% of the N exports from the plot in tree pruning (194 kg [N] ha^–1 yr^–1) originated from N₂ fixation. Grass production averaged 13 Mg ha^–1 yr^–1 and N export in cut grass was 195 kg [N] ha^–1 yr^–1. The total N fixed by G. sepium, as estimated from the tree and grass N exports and the increase in soil N content, was about 555 kg [N] ha^–1 yr^–1. Carbon sequestration averaged 1.9 Mg [C] ha^–1 yr^–1 and soil organic N in the 0-0.2 m layer increased at a rate of 166 kg [N] ha^–1 yr^–1, corresponding to 30% of N₂ fixation by the tree. Nitrogen released in nodule turnover (10 kg [N] ha^–1 yr^–1) and litter decomposition (40 kg [N] ha^–1 yr^–1) contributed slightly to this increase, and most of the recycled N came from the turnover or the activity of other below-ground tree biomass than nodules. This revised version was published online in June 2006 with corrections to the Cover Date.     

Irbic acid, a dicaffeoylquinic acid derivative from Centella asiatica cell cultures

3,5-O-dicaffeoyl-4-O-malonilquinic acid (1) (irbic acid) has been isolated for the first time from cell cultures of Centella asiatica and till now it has never been reported to be present in the intact plant. Evidence of its structure was obtained by spectroscopic analyses (MS/NMR). Besides 1, cell cultures produce also the known 3,5-O-dicaffeoylquinic acid, chlorogenic acid, and the triferulic acid 2 (4-O-8′/4′-O-8″-didehydrotriferulic acid). Biological activities were evaluated for compound 1, which showed to have a strong radical scavenging capacity, together with a high inhibitory activity on collagenase. This suggests a possible utilization of this substance as a topical agent to reduce the skin ageing process.     

Measuring nitrogen fixation by <Emphasis Type="Italic">Sesbania sesban</Emphasis> planted fallows using <Superscript>15</Superscript>N tracer technique in Kenya

A field experiment was performed in eastern Kenya to estimate N₂ fixation by Sesbania sesban over an 18-month period using the ¹⁵N dilution method. The influence of three reference species, Senna spectabilis, Eucalyptus saligna and Grevillea robusta, on the estimates of N₂ fixation was also assessed. Percentage Ndfa (nitrogen derived from the atmosphere) was calculated based on foliar atom excess (FAE), above-ground atom excess (AAE) or whole tree atom excess (WAE) data. The differences in atom% ¹⁵N excess values between species and plant parts are presented and discussed. We recommend the use of several reference species for estimating %Ndfa and that the different results obtained should be carefully considered in relation to the issues being addressed. In this study, Senna was the most suitable of the three reference species because its N uptake pattern and phenology were very similar to those of Sesbania. When well established, the amount of N fixed by Sesbania accounts for more than 80% of its total N content, according to FAE-based estimates. We estimated the Ndfa by Sesbania after 18 months to between 500 and 600 kg ha⁻¹ , depending on whether FAE, AAE or WAE data were used and on the choice of reference species. The substantial accumulation of N in planted Sesbania highlighted its potential to increase the sustainability of crop production on N-limited soils. We consider the ¹⁵N dilution method to be appropriate for quantifying N₂ fixation in improved fallows in studies, similar to this one, of young trees with high N₂-fixing ability.     

Heartwood extractives from the Amazonian trees <Emphasis Type="Italic">Dipteryx odorata,Hymenaea courbaril</Emphasis>, and <Emphasis Type="Italic">Astronium lecointei</Emphasis> and their antioxidant activities

Heartwood extracts from Amazonian trees cumaru-ferro (Dipteryx odorata), jatoba (Hymenaea courbaril), and guarita (Astronium lecointei) exhibit antioxidant activities comparable with that of α-tocopherol, a well-known antioxidant. This article reports the characterization of the antioxidant compounds in the extracts of the three heartwoods. Silica gel column chromatography of the cumaru-ferro EtOAc extract yielded (−)-(3R)-7,2′,3′-trihydroxy-4′-methoxyisoflavan and (+)-(3R)-8,2′,3′-trihydroxy-7,4′-dimethoxyisoflavan. Silica gel column chromatography followed by preparative high-performance liquid chromatography of the jatoba EtOAc extract yielded (−)-fisetinidol and (+)-trans-taxifolin. Chemical structures were assigned using electron-ionization mass spectrometry, ¹H and ¹³C nuclear magnetic resonance (NMR) spectroscopy including nuclear Overhauser effect spectroscopy (NOESY), as well as optical rotation and circular dichroism. Gas chromatography-mass spectrometry demonstrated that the isolated compounds were predominant in the EtOAc extracts. In the guarita EtOAc extract, catechin and gallic acid were identified by comparing their retention times and mass fragmentation patterns with those of authentic samples. Antioxidant activity determined by the 1,1-diphenyl-2-picrylhydrazyl assay demonstrated that all these compounds had activities comparable with that of α-tocopherol. Part of this report was presented at the 57th Annual Meeting of the Japan Wood Research Society, Hiroshima, August 2007     

Structure of xylan from culms of bamboo grass (Sasa senanensis Rehd.)

Xylan prepared from culms of kumaizasa (Sasa senanensis Rehd.), a representative species of bamboo grass, was hydrolyzed with-xylanase ofStreptomyces olivaceoviridis E-86. Four arabinoxylo-oligosaccharides and two glucuronoxylo-oligosaccharides were isolated from the enzymatic hydrolysate of the xylan by chromatography on a charcoal column, a Dowex 1-x8 column, a Toyo-pearl HW-40S column, and a LiChrospher 100 NH₂ column and on preparative paper chromatography. The results of the structural analyses of the saccharides showed that the isolated oligosaccharides had the structures of 3²--l-arabinofuranosyl-xylobiose, 3²--l-arabinofuranosyl-xylotriose, 3²--[-d-xylopyranosyl-(1 2)-l-arabinofuranosyl]-xylobiose, 3³--[-d-xylopyranosyl-(1 2)-l-arabinofuranosyl]-xylotriose, 2³--4-O-methyl-d-glucuronosyl-xylotriose, and 2³--d-glucuronosyl-xylotriose. From the structural analysis of the oligosaccharides derived from the xylan, kumaizasa xylan was concluded to be a kind of arabinoglucuronoxylan having not only stubs of singlel-arabinose and singled-glucuronic acid but also stubs of disaccharide units such as-d-xylopyranosyl-(1 2)-l-arabinofuranose.     

Phytochemical and antifungal studies on Terminalia mollis and Terminalia brachystemma

Phytochemical investigation of the stem bark of Terminalia mollis afforded friedelin (1), catechin with epicatechin (2), gallocatechin with epigallocatechin (3) and 3-O-methylellagic acid 4'-O-α-rhamnopyranoside (4). Arjunolic acid with 2α, 3β, 23-trihydroxy-urs-12-en-28-oic acid (5), 2α-hydroxyursolic acid (6), gallic acid (7), chebulanin (8) and 2'-O-galloylvitexin (9) were isolated from the leaf. Chebulanin (8), betulinic acid (10), ursolic acid (11), catechin (12), isoorientin (13), orientin (14), isovitexin (15) and punicalagin (16) were isolated from Terminalia brachystemma leaf. The first full unambiguous NMR assignments for (4) and (8), and revised assignments for (9), are reported. Compound (16) showed good activity against three Candida species.     

A new arylnaphthalene lignan from Knema furfuracea

A new arylnaphthalene lignan, named furfuracin (1), was isolated from the leaves of Knema furfuracea (Myristicaceae), whereas 7 known compounds including (+)-trans-1,2-dihydrodehydroguaiaretic acid, fragransin A₂, biochanin A, gingkolic acid, anarcardic acid, 2-hydroxy-6-(12-phenyldodecyl)-benzoic acid and 2-hydroxy-6-(12-phenyldodecen-8′Z-yl)-benzoic acid were obtained from its stems. The structure of the new lignan was established by analysis of spectroscopic data (UV, IR, MS and NMR).     

Two new chalcone glycosides from the stems of Entada phaseoloides

Two new chalcone glycosides 4′-O-(6″-O-galloyl-β-d-glucopyranosyl)-2′,4-dihydroxychalcone (1) and 4′-O-(6″-O-galloyl-β-d-glucopyranosyl)-2′-hydroxy-4-methoxychalcone (2) together with one known chalcone glycoside 4′-O-β-d-glucopyranosyl-2′-hydroxy-4-methoxychalcone (3) were isolated from the stems of Entada phaseoloides. The structures of the new compounds were elucidated on the basis of extensive spectroscopic analysis, including HSQC, HMBC, ¹H–¹H COSY, and chemical evidences. This is the first report of chalcone-type compounds isolated from the genus Entada.     

Effects of side-chain hydroxyl groups on pyrolytic <Emphasis Type="Italic">β</Emphasis>-ether cleavage of phenolic lignin model dimer

Effects of side chain hydroxyl groups on pyrolytic β-ether cleavage of phenolic model dimers were studied with various deoxygenated dimers under pyrolysis conditions of N₂/400°C/1 min. Although phenolic dimer with hydroxyl groups at the C _α ⁻ and C _γ ⁻positions was much more reactive than the corresponding nonphenolic type, deoxygenation at the C _γ -position substantially reduced the reactivity up to the level of the nonphenolic type. These results are discussed with the cleavage mechanism via quinone methide intermediate formation, which is activated through intramolecular hydrogen bonds between C _α ⁻ and C _γ ⁻ hydroxyl groups.