Vibsanin O, a novel diterpenoid from Viburnum awabuki

Vibsanin O, isolated from the leaves and twigs of Viburnum awabuki, is an unprecedented bicyclic diterpenoid. The structures of vibsanin O was established by extensive analysis of spectroscopic data.     

田间珊瑚树净光合速率及生态因子的日变化

自然条件下 ,对珊瑚树叶片光合作用日进程的研究结果表明 :夏季晴天珊瑚树阳叶净光合速率日进程曲线为“双峰”型 ,光合效率午间明显降低 ,主要由非气孔限制引起 .应用逐步多元回归方法 ,得到珊瑚树净光合速率日变化的最优方程为 :Y =- 4 9.8837 0 .0 10 3X1 0 .0 6 75X4 0 .4 913X5(复相关系数R =0 .84 12 ,F值 =4 .84 2 9,显著水平p =0 .0 4 82 ) .偏相关分析和通径分析表明 ,光合有效辐射、空气相对湿度和空气CO2 浓度与净光合速率的日变化有着极显著和显著的相关关系 ,是影响净光合速率的直接主要因子 ,影响的大小顺序为 :光合有效辐射 >空气相对湿度 >胞间CO2 浓度     

In Vitro Inhibitory Effects of Viburnum opulus Bark and Flower Extracts on Digestion of Potato Starch and Carbohydrate Hydrolases Activity

One of the effective treatments for diabetes is to reduce and delay the absorption of glucose by inhibition of α-amylase and α-glucosidase in the digestive tract. Currently, there is a great interest in natural inhibitors from various part of plants. In the present study, the phenolic compounds composition of V. opulus bark and flower, and their inhibitory effects on in vitro potato starch digestion as well as on α-amylase and α-glucosidase, have been studied. Bark and flower phenolic extracts reduced the amount of glucose released from potato starch during tree-stage simulated digestion, with IC₅₀ value equal to 87.77 µg/mL and 148.87 µg/mL, respectively. Phenolic bark extract showed 34.9% and 38.4% more potent inhibitory activity against α-amylase and α-glucosidase, respectively, but the activity of plant extracts was lower than that of acarbose. Chlorogenic acid (27.26% of total phenolics) and (+)-catechin (30.48% of total phenolics) were the most prominent phenolics in the flower and bark extracts, respectively. Procyanidins may be responsible for the strongest V. opulus bark inhibitory activity against α-amylase, while (+)-catechin relative to α-glucosidase. This preliminary study provides the basis of further examination of the suitability of V. opulus bark compounds as components of nutraceuticals and functional foods with antidiabetic activity.     

Versatile cobalt complexes for initiating immortal ring‐opening polymerization (ROP) of lactide (LA), mediating living radical polymerization of t‐butyl acrylate (tBA) and catalyzing copolymerization of LA and tBA by combination of ROP and organometallic‐mediated radical polymerization

Low‐cost, highly active and versatile amino‐bis(phenolate) cobalt complexes are developed. The cobalt complexes can control living polymerization of different categories of monomers including lactide (LA) by immortal ring‐opening polymerization in argon and even in air and acrylate via living radical polymerization (LRP). The cobalt‐based catalysts were used for copolymerization of LA and acrylate. The immortal polymerization of LA using the cobalt complexes as initiators proceeds in argon and even in air and without the requirement for extensive drying techniques or inert atmosphere whilst retaining end‐group fidelity. The cobalt complexes are used to mediate LRP of t‐butyl acrylate (tBA) in methanol. The block copolymerization of LA and tBA catalyzed by single‐site cobalt organometallic catalyst is also reported for the first time. This cobalt system offers a versatile and green way to produce homopolymers and block copolymers.     

Acyl Fluorides in Late‐Transition‐Metal Catalysis

In this Review, we summarize the current state of the art in late‐transition‐metal‐catalyzed reactions of acyl fluorides, covering both their synthesis and further transformations. In organic reactions, the relationship between stability and reactivity of the starting substrates is usually characterized by a trade‐off. Yet, acyl fluorides display a very good balance between these properties, which is mostly due to their moderate electrophilicity. Thus, acyl fluorides (RCOF) can be used as versatile building blocks in transition‐metal‐catalyzed reactions, for example, as an “RCO” source in acyl coupling reactions, as an “R” source in decarbonylative coupling reactions, and as an “F” source in fluorination reactions. Starting from the cleavage of the acyl C?F bond in acyl fluorides, various transformations are accessible, including C?C, C?H, C?B, and C?F bond‐forming reactions that are catalyzed by transition‐metal catalysts that contain the Group 9–11 metals Co, Rh, Ir, Ni, Pd, or Cu.     

一种面向新型视频编码器的快速算法

为降低多功能视频编码标准(VVC)编码的复杂度,提出一种面向VVC的帧内快速编码算法.首先,根据视频内容的时空域相关性,使用反向传播(BP)神经网络对CU的划分深度进行预测;然后,使用统计概率对CU的划分模式进行选择;最后,编码时跳过不必要的划分模式以节省编码时间.实验结果表明,与原始编码器相比,该算法平均可节省59.82%的编码时间,且在同等编码质量情况下比特率的平均增加值(BDBR)仅为2.05%.     

A versatile method for the synthesis of substituted 1-aminohydantoin derivatives

An efficient and versatile method has been developed for the synthesis of 1-aminohydantoin derivatives which can be substituted at all the possible positions of the hydantoin ring. The starting materials are aldehydes, ketones, carboxylic acids and hydrazides as well as isocyanates readily available from commercial sources. The semicarbazide-type reaction product of an N-acyl-N′-(1-cyanoalkyl)hydrazine, obtained from the above materials by methods known from the literature, and an isocyanate is cyclized in the presence of a basic catalyst to yield 1-acylamino-4-imino-2-oxoimidazolidine derivatives whose acid catalyzed hydrolysis leads to 1-aminohydantoin derivatives in good to excellent yields. The last two steps are carried out in a single reaction medium.     

A New Phenolic Diglycoside Produced in Response to Copper Toxicity and a New Flavan Dimer from the Leaves of Viburnum ichangense (Hemsl.) Rehd.

A new phenolic digycoside 1 was produced as stress metabolite in the fresh leaves of Viburnum ichangense (Hemsl.) Rehd ., in response to abiotic stress elicitation by CuCl₂. The stress metabolite was characterized as 1‐O‐[α‐L ‐arabinofuranosyl(1→6)‐β‐D ‐glucopyranosyl]‐erythro‐1,2‐bis(4‐hydroxy‐3‐methoxyphenyl)propane‐1,3‐diol ( 1 ). A new flavan dimer, 2,3‐epoxyflavan‐3′,4′,5,7‐tetraol‐(4→8″)‐flavan‐3″,3′′′,4′′′,5′′′,6″‐pentaol ( 2 ), and two known compounds, hovetrichoside A ( 3 ) and asperglaucide ( 4 ), were also isolated. Their structures were established by spectroscopic means.     

Possibility to Biotransform Anthracyclines by Peroxidases Produced by Bjerkandera adusta CCBAS 930 with Reduction of Geno- and Cytotoxicity and Pro-Oxidative Activity

The aim of this study was to evaluate the bioremoval mechanism of anthracycline antibiotics by the white-rot fungus B. adusta CCBAS 930. The activity of oxidoreductases and levels of phenolic compounds and free radicals were determined during the biotransformation of anthraquinone antibiotics: daunomycin (DNR) and doxorubicin (DOX) by B. adusta strain CCBAS 930. Moreover, phytotoxicity (Lepidium sativum L.), ecotoxicity (Vibrio fischeri), genotoxicity and cytotoxicity of anthraquinone dyes were evaluated before and after biological treatment. More than 80% and 90% of DNR and DOX were removed by biodegradation (decolorization). Initial solutions of DNR and DOX were characterized by eco-, phyto-, geno- and cytotoxicity. Despite efficient decolorization, secondary metabolites, toxic to bacteria, formed during biotransformation of anthracycline antibiotics in B. adusta CCBAS 930 cultures. DNR and DOX metabolites did not increase reactive oxygen species (ROS) production in human fibroblasts and resazurin reduction. DNR metabolites did not change caspase-3 activity.     

基于多层膜偏振元件的软X射线磁光Faraday偏转测量

在北京同步辐射装置(BSRF)的3W1B软X射线光束线上利用自行研制的同步辐射软X射线综合偏振测量装置对Ni的M_2,3边附近(60—70 eV)进行了软X射线磁光(magneto-optical)法拉第效应(Faraday effect)的偏转测量,实验装置主要由起偏器,检偏器,样品架,圆形钕铁硼永磁铁和MCP探测器组成,偏振元件(起偏元件和检偏元件)均采用反射式非周期性Mo/Si宽带多层膜.实验采用反射起偏和反射检偏的模式,得到一系列能量范围在60—70 eV间的法拉第偏转角结果, 关键词： 软X射线 磁光Faraday效应 综合偏振测量装置 宽带多层膜