查询词典 dihydro-compound

Polar compounds, such as dihydro-alkyl furan-one, furandione, benzofuran, benzosazol, aldehydes and esters were also detected.

对部分极性化合物分析，检出了二氢烷基呋喃酮系列、呋喃二酮、苯并呋喃及少量醛类和酯类化合物。

To improve the cyano reactivity, cyano-terminated PPENs were prepared by the end-capping reaction of PPEN-OL with CBN; benzonitrile terminated polys were also prepared by the polycondensation of excess 4,4'-oxydianiline with 1,2-dihydro-2-(4-carboxyphenyl)-4-[4-(4-carboxyphenoxyl)phenyl]-phthalazinone, followed by end-capping with CBA. The polymers synthesized exhibited good solubility in NMP, DMAc and DMF, and were crosslinked to afford phenyl-s-triazine-containing polymers under the similar conditions.

为提高氰基活性，以对氯苯腈为原料，对PPEN-OL进行封端，设计合成了含氰端基的聚芳醚腈；以含二氮杂萘酮联苯结构二酸单体与4，4'-二氨基二苯醚为原料，经Yamazaki膦酰化缩聚，并用对氰基苯甲酸进行封端，合成了含氰端基的聚芳醚酰胺。

Their structures were characterized as dihydroconiferyl dihydro-p-coumarate, vanillin, apocynin, p-hydroxybenzaldehyde, syringaldehyde, syringic acid, syringylethanone,α-hydroxypropiosyringone, coniferyl aldehyde, dihydroconiferyl alcohol, 2-hydroxyphenylpropanol, and 3-hydroxy-4-methoxy-phenylethanol, respectively.

结果 从该植物中分离得到12个酚性化合物，其结构分别为二氢松柏醇二氢对羟基桂皮酸酯，香草醛，罗布麻宁，对羟基苯甲醛，丁香醛，丁香酸，丁香乙酮，α-羟基丁香丙酮，松柏醛，二氢松柏醇，2-羟基苯丙醇和3-羟基－4-甲氧基苯乙醇。

These dendritic NOBIN derived Schiff base ligands have been applied to titanium catalyzed hetero-Diels-Alder reaction of Danishefshy's diene and aldehydes, affording the corresponding 2-substituted 2, 3-dihydro-4H-pyran-4-one in quantitative yields and excellent enantioselectivities (up to 97. 2%ee). Comparing the reactivities and enantioselectivities of reaction catalyzed by the titanium complexes of these Schiff base ligands, it was found that a series of ligands L〓 were superior to the other three series of ligands L〓, L〓 and L〓, a significant positive NLE and a dendrimer effect existed in the L〓 dendritic catalyst system. The disposition of the dendritic wedges and the dendron size in the ligands were observed to have a significant impact on the enantioselectivity of the reaction.

NOBIN衍生的树枝状大分子希夫碱手性配体与钛形成的配合物在催化不对称杂Diels-Alder反应中的应用将得到的四个系列NOBIN衍生的树枝状希夫碱三齿手性配体与四异丙氧基钛形成的配合物用于催化Danishefsky's diene与醛的不对称杂Diels-Alder反应，通过反应条件的优化，获得了定量的收率和最高达97.2％ee值的对映选择性；考察了这四个系列NOBIN衍生的树枝状希夫碱钛配合物的催化活性和对映选择性，结果发现它们的活性次序依次为L〓≈L〓＞L〓＞L〓，对映选择性次序依次为L〓＞L〓＞L〓＞L〓。

Stable pharmaceutical compositions containing 8-chloro-6,11-dihydro-11-(4-piperidylidene)-5H-benzo[5,6] cycloheptic [1,2-b] pyridine and a DCL protective amount of a pharmaceutically acceptable basic salt such as calcium dibasic phosphate and an amount of at least one disintegrant, preferably two disintegrates such as microcrystalline cellulose and starch sufficient to provide dissolution of at least about 80% by weight of the pharmaceutical composition in about 45 minutes and suitable for oral administration to treat allergic reactions in mammals such as man are disclosed.

本发明公开了含有8－氯－6，11－二氢－11－（4－亚哌啶基）－5H－苯并［5，6］环庚三烯并［1，2－b］吡啶和DCL保护量的可药用碱性盐如磷酸氢钙以及其含量足以使至少约80％的药物组合物在约45分钟内溶解的至少一种崩解剂、优选两种崩解剂如微晶纤维素和淀粉并且适于口服给药以治疗哺乳动物、例如人的过敏反应的稳定的药物组合物。

In some cases, its epimer 4 was also obtained. 22 compounds were synthesized, among them 18 were new.3. Using the intramolecular Pictet-Spengler reaction to form the pentacyclic skeleton of Et-743, the byproducts 25 were obtained under various conditions. The structures of them were determined to be 1, 2-dihydro-isoquinoline compounds, and the mechanism of the reaction was proposed.B. The synthesis of the analogs of Et-743Because of the failure of removing the protective groups in compounds 14, the synthetic strategy was adjusted.

对于苄基保护的羟基化合物13a，顺利得到化合物30，然后与不同的羧酸反应得到18个酯化合物33-50；对于苄氧羰基保护的氨基化合物13b，由于脱除保护基的化合物31在空气中不稳定，所以我们采取不经分离纯化，直接与羧酸反应得到酰胺化合物53-62，然后再分别对其C-21位的羰基进行还原氰基化，得到10个酰胺目标化合物63-72，另外，我们还对羟基转化为氨基的反应进行了探索。3。

Hydroxy-2,3-dihydro-4-quinolone is synthesized by the basic material of 4-nitrochloro-benzene. It has investigated the routes, conditions and purifies methods in this paper, which provides bases to lucubration and industrialization. This study belongs to the field of medical intermediates.

本文以4-硝基氯苯和丙烯酸为基础原料合成6-羟基-2，3-二氢-4-喹啉酮，并对6-羟基-2，3-二氢-4-喹啉酮的合成条件和纯化方法进行了实验研究，为后续的深入研究和工业化生产提供依据。

C-(6,11-Dihydro-5H-dibenzoazepin-6-yl)-methylamine was an important intermediate product of Epinastine hydrochloride.

C-(6，11-二氢-5H-二苯氮杂卓-6-烷)-甲胺是盐酸依匹斯汀的重要中间体，它是由5，11-二苯氮杂卓-6-腈经过还原反应制得，是合成该药的关键步骤。

AIM To investigate the effect of methyl pentyl 1,4 dihydro 2,6 dimethyl 4 (3 nitrophenyl) 3,5 pyridinedicarboxylate (MN9202),a dihydropyridine calcium antagonist, on cardiac indexes,ultrastructure, superoxide dismatase,glutathione peroxidase activity and malondialdehyde concentration in cardiac hypertrophy induced by L thyroxine in rats.

连续 12 d ip L- Thy0 。5 mg·kg- 1 · d- 1 复制大鼠心肌肥厚模型，实验组 ip MN92 0 2 0 。4mg· kg- 1· d- 1 ，2 mg·kg- 1· d- 1 ，10 mg· kg- 1· d- 1 ，阳性对照组 ip卡托普利 2 5 mg· kg- 1 · d- 1 ，模型组、对照组给予等量溶剂，于给药后的第 13日处死大鼠，检测心脏指数，电镜观察心肌组织的超微结构变化，化学比色法测定心肌匀浆中 SOD、GSH- PX活性和 MDA含量。

We examined the effects and mechanisms of methyl pentyl 1,4-dihydro-2,6-dimethyl-4-(3-notrophenyl)-3,5-pyridinedicarboxylate (Mn9202), a novel DHPs calcium antagonist and lacidipine on the 5-HT2B receptor in cultured rat stomach fundus smooth muscle cells.

本研究以富含5-HT_(2B)受体的大鼠胃底平滑肌细胞为模板，观察了二氢吡啶类钙拮抗剂2，6-二甲基-4-（3-硝基苯基）-1，4-二氢-3，5-吡啶二羧酸-3-甲酯-5-正戊酯（Mn9202）、拉西地平对 5-HT_(2B)受体功能的影响，并对其影响机制进行了较为深入的研究。

I didn't watch TV last night, because it .

昨晚我没有看电视，因为电视机坏了。

Since this year, in a lot of villages of Beijing, TV of elevator liquid crystal was removed.

今年以来，在北京的很多小区里，电梯液晶电视被撤了下来。