甘氨酰

Degradation of long residual herbicides and antidotal effective of TNA were tested by means of using bioassay methods combined in greenhouse and field test.

利用生物化学的方法研究谷胱甘肽转移酶、乙酰乳酸合酶、苯丙氨酸解氨酶和超氧化物歧化酶在除草剂作用下的反应和作保灵对相关酶、GSH，脯氨酸和多酚含量调控作用。

Objective To evaluate the efficacy and safety of N-acetylcysteine and glutathione in treating chronic hepatitis B patients.

目的 观察N-乙酰半胱氨酸和还原型谷胱甘肽治疗慢性乙型肝炎重度患者的临床疗效和安全性。

Trans-3-phenylglycidate ethyl ester was prepared from benzaldehyde and ethyl chloroacetate through Darzens condensation reaction.

以苯甲醛和氯乙酸乙酯为原料，经Darzens 缩合反应合成了反式-3-苯基缩水甘油酸乙酯，然后在25℃以氨水开环得赤型-3-苯基异丝氨酰胺。

Isovaleric, Methylmalonic, and Propionic Acid Decrease Anesthetic EC 50 in Tadpoles, Modulate Glycine Receptor Function, and Interact with the Lipid 1,2-Dipalmitoyl- Sn -Glycero-3-Phosphocholine1,2

甲基丙二酸、丙酸减小蝌蚪的麻醉药EC50，调节甘氨酸受体功能，和1，2-二棕榈酰 sn 甘油-3-胆碱磷脂相互作用

Isovaleric, Methylmalonic, and Propionic Acid Decrease Anesthetic EC50 in Tadpoles, Modulate Glycine Receptor Function, and Interact with the Lipid 1,2-Dipalmitoyl- Sn -Glycero-3-Phosphocholine

蝌蚪实验显示异戊酸、甲基丙二酸及丙酸能减少麻醉药物 EC50值，调节甘氨酸受体功能以及与二棕榈酸磷脂酰胆碱相互作用

The paper discusses the preparation of stearic bicine diester for sizing agent and its application in paper-making.

论述了双硬脂酰取代甘氨酸酯施胶剂的制备及其在造纸中的应用。

In order to obtain versatile ulitity of host molecules, three new chiral calix [4] crown ethers containing aza, thio atoms bearing two chiral sites provided by -cysteine ester were synthesized by the condensation of calix [4] arene diacid dichloride with oligoethylene glycol bridged bis-amino acid methyl ester. All new compounds were characterized by NMR, MS and elemental analysis.

以-半胱氨酸为手性源，利用多甘醇二氯醚在碱性条件下对半胱氨酸巯基进行烷基化反应，成功地合成了多甘醇醚链桥联的半胱氨酸衍生物，醚化反应后，在高度稀释条件下与对叔丁基杯[4]芳烃二乙酰氯进行双功能基缩合反应成功地合成了新型的手性杯[4]含氮、硫杂冠醚，并利用〓H NMR、MS等谱图手段对其结构进行了表征。

The results showed that the addition leading to -2-phenyl-2-(2-vinylpiperidin-1-yl) ethanol 7 could proceed with good diastereoselectivity and excellent yield (95%).(3) The selective N-deprotection of -2-phenyl-2-(2-vinylpiperidin-1-yl) ethanol 2 without affecting the vinyl group in the substrate were untaken.(4) The Zip reaction for the transformation of -1-(3-aminopropyl)-3-methylazecan-2-one 8 to -7-Methyl-1, Sdiaza-cyclotetradecan-6-one 9 were undertaken. The results showed that, under controlled conditions, acceptable yields (43%) could be achieved and racemization can be minimized during the ring expansion reaction.

该合成路线与文献方法相比，反应条件较温和，也缩短了反应时间；(2)哌啶衍生物2与乙烯基格氏试剂进行加成反应的条件和立体选择性，取得了较好的结果（差向异构体比为80：20，产率95％左右）；(3)不饱和哌啶衍生物7在不影响碳碳双键的情况下去除苯基甘氨醇手性辅助基的条件；(4)具有羰基α位手性的氨基酰胺8在不同条件下经Zip重排反应转变为9的反应，控制反应条件，可使反应中消旋化减小到最小的程度。

Employing CuI(5 mol%), N,N-dimethylglycine hydrochloride(10 mol%) and K_2CO_3(2 equiv.) in refluxing THF as the optimized reaction conditions,the four-membered 4-alkylidene-2-azatidinones could be efficiently synthesized.

当以3-溴-3-N-苯基-丁烯酰胺为底物，在5 mol%CuI为催化剂，10 mol%N，N-二甲基甘氨酸盐酸盐为配体，2当量K_2CO_3作碱，THF回流的反应条件下，可以高效的合成2-亚甲基-4-氮杂环丁酮类化合物。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。