1) oxa-Michael addition
oxa-Michael加成
1.
The selective formation of C-N bond and microwave-assisted intramolecular oxa-Michael addition reaction were studied in this thesis.
本论文对选择性C-N键的形成及微波辅助分子内oxa-Michael加成反应进行了研究。
2) oxa-Michael reaction
oxa-Michael加成反应
1.
Although oxa-Michael reaction is an important protocol and often applied in the total synthesis of natural products,it has only recently gained considerable interest.
简要综述了oxa-Michael加成反应的研究进展。
3) Michael addition
Michael加成
1.
Synthesis of acyclic derivatives of adenine by Michael addition;
利用Michael加成合成腺嘌呤无环衍生物
2.
Progress on the catalytic asymmetric Michael addition reaction
不对称Michael加成反应的研究进展
3.
Asymmetric Michael addition of chiral imine of 4,4-ethylenedioxy-2-methylcyclo hexanone 2c with ethylvinylketone led to 2,2-disubstituted cyclanone(+)-5,(-),6,6-(ethylenedioxy)-1,10-dimethyl-1(9)-octal-2-one(1c) was obtained by Claisen condensation.
乙基乙烯基酮与4,4-乙二氧撑-2-甲基环乙酮2 c的手性亚胺进行不对称Michael加成,生成2,2-双取代环烷酮5,5经过克莱森缩合得到(-)-6,6-乙二氧撑-1,10-二甲基-1(9)-八氢萘酮-2(-)(1 c)。
4) Anti-Michael Additions
反-Michael 加成
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