反应的

The photocycloaddition of 1-naphthonitrile (1-NpCN) and 2,3-dimethyl-2-butene in cyclohexane or benzene gave cyclobutane 3 primarily,but that of 2-NpCN gave azetine 6 asthe major and cyclobutane 5 as the minor product in low conversion photolysis.

在低转化光解情况下，1-萘甲腈(1-NpCN)和2，3-二甲基丁烯-2在环已烷或苯中的光环加成反应主要得到环丁烷3，但2-NpCN主要得到氮杂环丁烯6和少量的环丁烷5，三氟醋酸量增加抑制1-NpCN和DMB的光环加成反应，表明TFA与基态及单激发态1-NpCN生成非光反应的复合物，它也淬灭(1-NpCN-DMB)激基复合物。

The photocycloaddn. of 1-naphthonitrile (1-NpCN) and 2,3-dimethyl-2-butene in cyclohexane or benzene gave cyclobutane I primarily, but that of 2-NpCN gave azetine II as the major and cyclobutane III as the minor product in low conversion photolysis. The photocycloaddn. of 1-NpCN with DMB is retarded by increasing amts. of trifluoroacetic acid which is shown to form non-photoreactive complexes with ground state as well as with singlet excited state 1-NpCN. It also quenches the *(1-NpCN-DMB) exciplex.

在低转光解情况下，1-萘甲腈(1-NpCN)和2，3-二甲基丁烯-2在环已烷或苯中的光环加成反应主要得到环丁烷3，但2-NpCN主要得到氨杂环丁烯6和少量的环丁烷5，三氟醋酸量增加抑制1-NpCN和DMB的光环加成反应，表明TFA与基态及单激发态1-NpCN生成非光反应的复合物，它也淬灭^*(1-NpCN-DMB)激基复合物。

In the second part of the thesis, we discussed a L-proline-catalyzed direct Aldol reaction between L-amino acid-derived N,N-dibenzyl -amino aldehydes 15 and acetone, cyclopentanone or hydroxyacetone, which afforded (-amino--hydroxy- or (-amino-,(-dihydroxy-ketones in good to excellent yields (up to 94%) and diastereoseletivities (up to 94.9%).

发现许多情况下，反应的产率和de值超过90%。接着，在碱性条件下，我们将L-亮氨酸衍生的N，N-二苄基--氨基醛15g与羟基丙酮反应得到的主要产物(，-二羟基-γ-氨基酮171d与次溴酸钠反应，得到了具有抗肿瘤活性的天然产物PM-94128的氨基酸片断184。

The effects of catalyst, deaquation reagent, reaction time and the ratio of raw materials on the reaction were examined.

考察了催化剂、带水剂、反应时间、物料比等因素对反应的影响。

A series of diethanolamine derivatives were synthesized,the main factors influencing the reactions were studied and the optimal reaction conditions were determined.

设计合成了一系列二乙醇胺衍生物，对各反应的主要影响因素进行了考察，确定了最优反应条件。

Disubstituted 2-isoxazolines were oxidized to corresponding isoxazoles by NO in dichloromethane.

所以反应的反应过程是受溶剂控制的。3、3，5-二取代的-2-异恶唑啉在NO作用下可以发生芳环化反应，生成对应的2-异恶唑化合物。

To further extend the scope of this type Cannizzaro disproportionation reaction and the reactivity of enolate ligand in complex with aldehyde,we designed to synthesis new rare earth complexes containing arylamido and.enolate mixed ligands,studied their reactivity with aromatic aldehydes for the disproportionation reaction.

为了进一步探索这种歧化反应的应用范围及配合物中作为配体的乙烯醇基与醛的反应性，我们设计合成了含胺基、乙烯醇基混合配体的新型稀土配合物，并研究了其与芳香醛的反应。

Ea for the concerted mechanism was 167.24 kJ/mol, while it was 155.20 kJ/mol for the formation of ethoxide intermediate in the stepwise mechanism.

比较苯与乙醇和乙烯发生烷基化反应的机理可以看出，二者作为烷基化试剂对烷基化反应性能影响不大。

The Faradaic impedance was analyzed and characterized by the Volmer reaction....

反应的法拉第阻抗也同样取决于界面放电Volmer反应。

The expressions of current density and the Faradaic Impedance for the three-step electrode processes involving chemical adsorption,charge transfer and desorption steps in the presence or absence of a chemical competitive reaction have been derived in terms of linear condition in this paper,by which the effect of the chemical competitive reaction on the main reaction was analyzed.

在线性条件下，推导了由化学吸附、电荷传递、化学脱附三步骤的电极过程在有化学竞争反应条件下的电流密度和法拉第阻抗的表达式，分析了不同条件下化学竞争反应对主反应的影响，并使用等效电路对可能出现的阻抗结果进行了理论描述。

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！