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1)  Abiko's anti-selective aldol reaction
Abiko反式羟醛缩合
2)  anti-aldol reaction
反式Aldol羟醛缩合
3)  aldol reaction
羟醛缩合反应
1.
Small organic molecules catalyzed asymmetric aldol reaction is reviewed.
总结了近年来用于不对称催化羟醛缩合反应的各种有机小分子催化剂,简要阐述了每种类型的催化剂的催化机理以及它们的优缺点,同时对有机小分子催化反应的发展进行了展望。
4)  aldol condensation
羟醛缩合反应
1.
Trimethylolheptane (TMH) was synthesized through consecutive aldol condensation and Cannizzaro reaction of octylaldehyde and formaldehyde, using sodium hydroxide as catalyst.
以氢氧化钠为催化剂,辛醛和甲醛在较低温度下发生羟醛缩合反应生成2,2-二羟甲基辛醛。
2.
2,2-Dimethyloldodecanoic acid was synthesized using lauric aldehyde,formaldehyde and hydrogen peroxide as regents through aldol condensation and oxidation reactions.
研究了以月桂醛(正十二醛)、甲醛、过氧化氢为原料,经羟醛缩合、过氧化氢氧化合成2,2-二羟甲基十二酸的方法,探讨了原料摩尔比、催化剂或氧化剂用量、反应温度和时间对羟醛缩合反应和氧化反应的影响。
3.
The title compounds were synthesized by the aldol condensation reaction of 2,3-dihydropyrano[2 3-f]isoquinolin-4-one and substituted furaldehyde under the alkaline condition.
由2 ,3 - 二氢- 4 H- 砒喃并[2 ,3 - f] 异喹啉- 4 - 酮与取代糠醛为原料,通过碱性催化的羟醛缩合反应合成了标题化合物,通过元素分析, I R 和 N M R 光谱确定了全部新化合物的结构,并讨论了反应机理。
5)  aldol condensation
羟醛缩合
1.
Study on aldol condensation reaction of cyclohexanone catalyzed by solid superbase
固体超强碱催化环己酮羟醛缩合反应的研究
2.
A novel second-order nonlinear optical chromophore(DCDHF-2-V) was synthesized from 3-Hydroxy-3-methyl-2-butanae,propanedinitrile and 4-diethylaminobenzaldehyde by aldol condensation reaction.
用3-羟基-3-甲基-2-丁酮、丙二腈和N,N-二乙基对苯甲醛,经羟醛缩合反应制备了一种新型有机小分子二阶非线性光学(NLD)材料DCDHF-2-V。
3.
The prospect of the catalysts for aldol condensation is also been put forward.
羟醛缩合可以形成新的碳-碳键,增长碳链,是一类重要的有机反应。
6)  cross-aldol condensation
交叉羟醛缩合反应
1.
The comparative investigation of synthesizing the polyhydric alcohols, such as pentaerythritol, pentaglycerine, trimethylolpropane, neopentyl glycol and so on are conducted, these compounds are all based on the reaction of cross-aldol condensation.
对季戊四醇、三羟甲基乙烷、三羟甲基丙烷、新戊二醇等基于交叉羟醛缩合反应的多元醇类化合物的合成进行对比研究。
补充资料:[3-(aminosulfonyl)-4-chloro-N-(2.3-dihydro-2-methyl-1H-indol-1-yl)benzamide]
分子式:C16H16ClN3O3S
分子量:365.5
CAS号:26807-65-8

性质:暂无

制备方法:暂无

用途:用于轻、中度原发性高血压。

说明:补充资料仅用于学习参考,请勿用于其它任何用途。
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