氧化合物

One of these compounds, 2-diethyl- aminoethyl-5--(4-methoxybenzylidene) cyclo- pentanone hydrochloride (T81) possessed sig- nificant antiinflammatory and analgesic ac- tivity when administered orally.

Ⅲ类化合物完全无抗癌活性，对其中一个化合物2-二乙胺乙基-5--（4-甲氧基苯亚甲基）环戊酮盐酸盐（T81）试验结果表明，它经口给药时具有显著的抗炎、镇痛活性。

Hydroxylethyl peroxyl radical was chosen to act as a model of lipid peroxyl radical in thekinetic studies of its reaction with several typical flavonoids.

本论文选择了α-羟乙基过氧自由基作为脂质过氧自由基的模拟物，研究了它与几种典型的黄酮类化合物的反应动力学。

Four novel methoxycarbonylindole-3-carboxaldehyde phenylhydrazone s were synthesized by the condensation reaction between methoxycarbonylindole-3-carboxaldehyde and phenylhydrazine in acidic condition.

甲氧羰基吲哚-3-甲醛与苯肼在酸性条件下通过缩合反应合成了4个未见文献报道的新化合物甲氧羰基吲哚-3-甲醛苯腙，其结构经1HNMR，IR和MS确证。

Four novel methoxycarbonylindole-3-carboxaldehyde phenylhydrazones were synthesized by the condensation reaction between methoxycarbonylindole-3-carboxaldehyde and phenylhydrazine in acidic condition.

甲氧羰基吲哚-3-甲醛与苯肼在酸性条件下通过缩合反应合成了4个未见文献报道的新化合物甲氧羰基吲哚-3-甲醛苯腙，其结构经1HNMR，IR和MS确证。

Four new compounds,substituted-benzyloxyindole-3-formaldehyde-(4′-nitro) phenylhydrazone ,were synthesized by the condensation of 4-nitrophenylhydrazine with substituted-benzyloxyindole-3-formaldehyde in ethanol.

以取代苄氧基吲哚-3-甲醛和4-硝基苯肼为原料，乙醇为溶剂，通过缩合脱水反应合成了4个新化合物——取代苄氧基吲哚-3-甲醛-(4′-硝基)苯腙，其结构经1H NMR，IR，MS和元素分析表征。

Twenty-seven compounds were isolated from the methanol extract of the stems of Pinus massoniana by means of chromatographic methods, and their structures were elucidated as 8(14),15-Pimaradien-19-oic acid (1), Pimaric (2), Podocarpic acid (3), 12-Hydroxydehydroabietic acid (4), Dehydroabietic acid (5), 15-Hydroxydehydroabietic (6), 3β-Methoxyserrat-14-en-21-one (7), 3β-Hydroxy- serrat- 14-en-21-one (8), 3β-Methoxyserrat-14-en-21-one-30-al (9),(24R)-Stigmst- 4-ene-3-one (10),β-sitosterol (11),-3-Hydroxy-5-methoxy-stilbene(12), 4-Hydroxy-3- methoxycinnamaldehyde (13),-Ferulic acidtetracosyl ester (14), Alkylferulates (15), Pinocembin (16), Coniferaldehyde (17), Matairesinol (18),-Nortrachelogenin (19), Balanophonin (20), Cedrusin (21),-Pinoresinol (22), Tanegoside (23), 1,2-Bis-(4-hydroxy-3- methoxyphenyl)-propane-1,3-diol (24),(1S*, 2S*)-1-(4- Hydroxyphenyl) glyceri...

同时对马尾松枝条的甲醇提取物利用各种色谱技术进行了分离纯化，并利用现波谱技术鉴定了27个化合物的结构，分别为：8(14)，15-Pimaradien-19-oic acid (1)、海松酸(2)、罗汉松酸(3)、12-羟基脱氢松香酸(4)、脱氢松香酸(5)、15-羟基-脱氢松香酯(6)、3β-甲氧基-锯齿石松-14-烯-21-酮(7)、3β-Hydroxyserrat-14-en-21-one (8)、3β-Methoxyserrat-14-en-21– one-30-al (9)、(24R)-豆甾-4-烯-3-酮(10)、-3-羟基-5-甲氧基-二苯乙烯(12)、4-Hydroxy-3-methoxycinnamaldehyde (13)、-Ferulic acidtetracosyl ester (14)、Alkylferulates (15)、Pinocembin (16)、Coniferaldehyde (17)、罗汉松树脂酚(18)、 Balanophonin (20)、tanegoside (23)、1，2-Bis-(4-hydroxy- 3-methoxyphenyl)-propane- 1，3-diol (24)、(1S*，2S*)- 1-(4-hydroxyphenyl)glycerins (25)、(1R*，2R*)-1-(4-hydroxy- phenyl)gly-cerins (26)和赤松素(27)。

The beta-thioalkoxyalcohols could be obtained in good yields by the reaction of dialkyl-substituted propargylic dithioacetals with a series of carbonyl compounds.

我们发现在铁触媒和格林那试剂的存在下，利用双烷基取代炔丙基硫缩酮和羰基化合物反应生成的beta-硫烷氧基醇，可以进行不常见的beta-氧消去反应，而得到烯炔衍生物。

Aim To design and synthesize a serial of 1,5-diaryl pyrazole derivatives and to study their COX-2 inhibitory activities .

所有目标化合物均具有一定的环氧合酶2抑制活性，其中化合物1i的抑制率为31。

In thesecond chapter, eleven 1,3,4-oxadizoles bearing chiral pyrazolyl moieties(4a-k) andfive triazolotriazines bearing chiral pyrazolyl moieties(5a-e) were obtained from5-[(1"S)-1",2-diacetyl-oxyethyl]-1-phenylpyrazol-3-carboxaldehyde(1) with arylcar-bohydrazide or (5-aryl-1,2,4-triazin-3-yl)hydrazine through an intramolecular1,3-dipolar cycloaddition in the presence of the non-metal oxidant IBD.

其中第二章介绍了以D-葡萄糖为原料制得的5-[(1′S)-1′，2′-二乙酰氧基乙基]-1-苯基吡唑-3-醛(1)分别与芳基甲酰肼、(5-取代苯基-1，2，4-三嗪-3-基)肼反应，在无金属氧化剂—IBD引发下，发生分子内1，3-偶极环加成，采用&一锅煮&法合成了11种含手性吡唑基的1，3，4-噁二唑类化合物(4a-k)和5种含手性吡唑基的三唑并三嗪类化合物(5a-e)。

This paper reviews pathways of aerobic and anaerobic microbiological degradation of PCP. It can be concluded that reductively dechlorination prior to ring cleavage plays a key role in mineralization of PCP.

文章通过综述好氧与厌氧微生物降解五氯酚的降解菌和降解途径，认为五氯酚首先通过脱氯转化为低氯代化合物后再开环，因此脱氯就成为五氯酚降解的关键步骤。

She gently rebuff ed him, but agreed that they could be friends

她婉言拒绝了，但同意作为朋友相处。

If in the penal farm, you were sure to be criticized.

要是在劳改农场，你等着挨绳子吧！