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Then,the oxidation ofβ-ionone catalyzed by CMPS-Co_2 has been performed,andβ-ionone was oxidized to 4-oxo-β-ionone as the main product,and the influence of a series of different conditions for the reaction was also investigated.

首先将催化剂CMPS-Co_2应用于β-紫罗兰酮的催化氧化,主要得到4-氧代-β-紫罗兰酮,并考察了不同反应条件对β-紫罗兰酮选择性氧化的影响。

A total of 54 products were identified, including β-damascone, 4-oxo-β-ionone, 3,4,4-trimethyl-2-cyclohexen-1-one and 2,5,5-trimethyl-cyclohex-3-en-1-one.

根据4-氧代-β-大马酮裂解产物相对含量的变化规律,对其裂解产物的形成机理进行了探讨,认为4-氧代-β-大马酮可能按照4种途径发生裂解。

A series of L-histidine Schiff bases that include Sal-His (H2L^1), Br-Sal-His(H2L^2), NO2-Sal-His (H2L^3) and their Cu complexes were synthesized, and the catalytic behavior of Schiff-base-Cu for the oxidation of β-ionone to 4-oxo-β-ionone as well as the effects of substitutents on these properties were examined.

合成了芳环上含不同取代基的Schiff碱配体(水杨醛缩组氨酸(H2L^1)、5-溴水杨醛缩组氨酸(H2L^2)、5-硝基水杨醛缩组氨酸(H2L^3)及其铜配合物,研究了其作为催化剂应用于催化分子氧氧化β-紫罗兰酮制备4-氧代-β-紫罗兰酮中的行为。

The results indicated that β-ionone was catalytically oxidized to 5,6-epoxy-β-ionone, 4-oxo-β-ionone, 4-hydroxy-β-ionone, and a little dihydroactinidiolide.

结果表明,催化剂的催化性能与担载金的颗粒大小密切相关,同时溶剂的性质也对反应有明显影响。

The main product was 4-oxo-β-ionone with a yield of 50.2% and a purity over 98.5% under O2 pressure(1MPa) at 75℃ with additive pyridine over catalyst CuL^2 in 10h.

以CuL^2作催化剂,当反应时间为10h、反应温度为75℃、催化剂用量为1.6%、O2气压力为1MPa、添加摩尔分数为30%吡啶时,4-氧代-β-紫罗兰酮的收率为50.2%,纯度超过98.5%。

First, a series ofα-oxo ketene dithioacetals were preparated on the basis of our recent work.

具体研究如下:1。在十分温和的条件下,合成了一系列α-羰基二硫缩烯酮类化合物。2。

Therefore it is very important to explore the feadibility of clean synthesis lf complex compounds from a-oxo ketene dithioacetals

因此,以a-羰基二硫缩烯酮类化合物为合成子,探索复杂化合物的绿色合成方法将具有重要意义

Oxo ketene dithioacetals are a kind of versatile intermediates in organicsynthesis. It can be widely used in forming aromatic and heterocyclic compounds.

α-羰基二硫缩烯酮类化合物是一类重要的有机合成中间体,广泛应用于芳环和杂环化合物的合成中。

Second, we investigated the aldol reactions of the specialα-oxo ketene dithioacetals with aromatic aldehydes under the mild conditions in good yields.

在温和的条件(室温、30℃)下,高产率地实现了α-羰基二硫缩烯酮与芳香醛的缩合反应。3。

Among the variousα-oxo ketene dithioacetals,α-alkenoyl ketene dithioacetals are easier to prepare and bear much more functionalities.

在众多的α-羰基二硫缩烯酮类化合物中,α-烯酰基二硫缩烯酮具有易于制备,官能团多等特点。

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This one mode pays close attention to network credence foundation of the businessman very much.

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