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Cyclopentene ; oxidation ; cyclopentanone ; palladium acetate ; iron phthalocyanine

环戊烯;氧化;环戊酮;醋酸钯;酞菁铁

The effect of cyclopentene concentration palladium salts, FePc, acid and reaction mechanism were discussed.

在乙腈的酸性水溶液中,考察了 Pd Ac2 /Fe Pc催化氧化环戊烯合成环戊酮的催化活性,讨论了影响该反应活性的因素及其反应机理。

Under the optimum conditions of a cyclopentene amount of 1.0 mol, a molar ratio of cyclopentene to water of 0.25, a reaction temperature of 120 ℃, a reaction time of 4.0 h, a main catalyst dosage of 4.0 g and a cocatalyst dosage of 0.8 g, the yield of cyclopentanol reached 68.6%.

确定适宜的反应条件为:环戊烯1.0 mol,n﹕n=1﹕4,反应温度120 ℃,反应时间4.0 h,硅胶负载铌酸主催化剂用量4.0 g,三(3,6-二氧杂庚基)胺助催化剂0.8 g。在此反应条件下,环戊醇收率68.6%。

Cyclopentanol was synthesized from cyclopentene and water through hydration reaction using HNb3O8·H2O/SiO2 as main catalyst and tris(dioxa-3,6-heptyl)amine (TDA-1) as cocatalyst.

在以硅胶负载铌酸为主催化剂、三(3,6-二氧杂庚基)胺为助催化剂的作用下,以环戊烯和水为原料,通过水合加成反应合成了环戊醇。

The Nazarov cyclization, a powerful tool for the construction of five-membered carbocycles from divinyl ketones and related compounds, has attracted increasing attention in recent years due to its wide applications in the synthesis of complex natural and unnatural products.

Nazarov环合反应是通过二烯酮类物质和类似化合物构建五元碳环的有效方法。由于该方法广泛地应用于复杂天然和非天然产物的合成,近年来引起人们的广泛关注。

The protic- or Lewis acid catalyzed ring-closure of divinyl ketones (and their acid-labile precursors) pentadienylic cations is known as the via Nazarov cyclization.

质子酸或路易斯酸通过戊二烯基阳离子催化二乙烯酮的环闭合(以及它们的酸不稳定前体)这个反应被称为Nazarov环化。

Total volatile components, acetone, cyclohexadiene, cyclopentyl ethyne, acetic acid and hexanal contents show more significant correlation with storage time, physiological biochemical indexes respectively, and it can be used as an assessment index for the storage quality of stored maize.

总挥发性物含量、丙酮、对环己二烯、环戊乙炔、乙酸、己醛的含量与储藏时间、生理生化指标呈较高相关性,可作为玉米储存品质变化的评判指标。

Dihydrojasmone was synthesized from2-hexyl-5-methyl-1,2-oxaborolane,prepared frommethyl vinyl ketone and hexene,via the homologationwith 〓 followed by PCC oxidation and intra-molecular condensation.In stead of the oxidation ofthe C-B bond of 1,2-oxaborolane,fluoride inducedhalogenation of 2-alkoxy-1,2-oxaborolane was found togive 3-halopropanol.

硼氢化甲基乙烯基酮和已烯得到的2-已基-5-甲基-1,2-氧硼杂环戊烷与〓反应,再经PCC氧化,分子内缩合得到二氢茉莉酮。1,2-氧硼杂环戊烷的C-B键除氧化断裂之外,也能够在〓或KF作用下卤化断裂成碳卤键。

Lactonization of 32 swiftly took place under basic condition, and the first four-ring intermediate 53 was gained.

以动力学烯醇化-氧化的方法,在18的〓位引入了〓羟基,解决了构成1,4-内酯环的相对立体化学问题。32在碱性条件下,顺利完成了1,4-内酯环的构筑,首次获得了四环中间体53。

A series of 3 - aryl - 3 -( 5,5 - dimethyl - 3 - hydroxy - 2 - cyclohexene - 1 - one - 2 - yl) propanoic ester s were synthesized by reaction between aromatic aldehydes ,5,5- dimethyl -1,3-cyclohexanedione and isopropylidene malonate catalyzed by KF - Al2O3 in alcohols.

在KF-Al_2O_3催化下,将芳香醛3,5-二甲基-1,3-环己二酮及丙二酸亚异丙酯在醇中反应,一锅式合成了一系列的3-芳基-3-(5,5-二甲基-3-羟基-2-环己烯-1-酮-2-基)丙酸酯。

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