1) homo-Michael reaction
homo-Michael反应
2) Michael reaction
Michael反应
1.
Proline-catalyzed direct asymmetric Michael reactions;
脯氨酸催化的直接不对称Michael反应
2.
Preparation of novel aliphatic sulfonie acid ion exchange resin by Michael reaction;
通过Michael反应制备脂肪磺酸基强酸型阳离子交换树脂
3.
With the action of phase transfer catalyst (PTC), N phthalyl β alanine methyl ester (PAME) was synthesized by Michael reaction with a mixture of phthalimide,methyl acrylate and K 2CO 3.
采用相转移催化法 ,以Michael反应合成了 β 酞酰亚胺基丙酸甲酯。
3) 1,4-Michael reaction
1,4-Michael反应
1.
2-(4-β-D-Allopyranosyloxyphenyl)-4-aryl-2,3-dihydro-1,5-benzothiazepine deriva-tives(2a～2e) have been synthesized by 1,4-Michael reaction with 1a～1e.
以豆腐果苷为原料,与4-取代苯乙酮发生Claisen-Schimidt反应,得到一系列E-4-β-D-吡喃阿洛糖苷-苯乙烯基-4-取代苯酮衍生物1a～1e,再将1a～1e与邻氨基苯硫酚发生1,4-Michael反应,得到2-(4-β-D-吡喃阿洛糖苷-苯基)-4-芳基-2,3-二氢-1,5-苯并硫氮杂衍生物2a～2e,以上化合物均未见文献报道,其结构经1H NMR,IR,MS加以确证,并对2a～2e进行了药理活性筛选。
4) Michael-type reaction
Michael式反应
5) Michael addition reaction
Michael加成反应
1.
KF/NaZnPO4 was used as the catalyst for Michael addition reaction of ethyl acetoacetate and acrylonitrile.
以磷酸锌钠负载KF为催化剂,催化乙酰乙酸乙酯与丙烯腈进行Michael加成反应。
2.
The post-modification was accomplished by acetalization, esterification and etherification of hydroxyl group of PVA as well as Michael addition reaction.
综述了聚乙烯醇(PVA)在醋酸乙烯共聚前后改性的方法和原理,前期改性是选用带有酰胺基、羧 基、环氧基、磺酸基的不饱和化合物与醋酸乙烯共聚;后期改性是通过PVA上醇羟基的缩醛化酯化、醚化等 化学反应以及Michael加成反应等实现。
3.
Michael addition reaction between poly (vinyl alcohol) (PVA) and propyl vinyl sulfoxide (PrVSO) was studied in sodium hydroxide aqueous solution.
本文研究聚乙烯醇与丙基乙烯基亚砜经Michael加成反应合成含亚砜基的改性聚乙烯醇功能高分子。
6) Michael addition
Michael加成反应
1.
Applications and the mechanisms of alumina-supported potassium fluoride in Michael addition reactions;
KF/Al_2O_3在Michael加成反应中的应用及其机理
2.
Studies on Michael Addition Catalyzed by a Highly Effective Catalyst-Y(OTf)_3;
新型高效催化剂Y(OTf)_3催化的Michael加成反应的研究
3.
Three N-L-alaninylated Betti bases have been designed and conveniently synthesized and evalu-ated as organocatalysts for the asymmetric Michael addition of cyclohexanone to nitroolefins.
合成了3个手性Betti碱的L-丙氨酰衍生物,并用它们来催化环己酮与硝基烯的Michael加成反应。
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。
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。
参考词条