Now Is The Time For You To Know The Truth About 100-19-6

Recommanded Product: 1-(4-Nitrophenyl)ethanone. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Zhang, S; Shi, XH; Li, JC; Hou, ZT; Song, ZH; Su, XF; Peng, D; Wang, F; Yu, YT; Zhao, GL or concate me.

Recommanded Product: 1-(4-Nitrophenyl)ethanone. Recently I am researching about N-ACYLIMINIUM IONS; NUCLEOPHILIC-SUBSTITUTION; PIPERIDINE; CHEMISTRY; EFFICIENT; DERIVATIVES; 2-POSITION; INHIBITORS; DN-2327; PROFILE, Saw an article supported by the Shandong Provincial Natural Science FoundationNatural Science Foundation of Shandong Province [ZR2017BB033]; Youth Science Funds of Shandong Academy of Sciences [2018QN0030]; National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [51503118]. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Zhang, S; Shi, XH; Li, JC; Hou, ZT; Song, ZH; Su, XF; Peng, D; Wang, F; Yu, YT; Zhao, GL. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone

An efficient Ni(ClO4)(2)center dot 6H(2)O-promoted amidoalkylation re-action for the synthesis of 3-substituted isoindolinones involving various gamma-hydroxy lactams and nucleophiles has been successfully developed. The transformation proceeds with both carbon (ketones and arenes) and heteroatom (alcohols, thiols, and amines) nucleophiles and in both intermolecular and intramolecular manners. The prominent features of the present strategy are wide substrate scope, excellent group tolerability, and moderate to good yields (up to 96% yield). The present strategy is also characterized by remarkable superiority over the current synthetic methods. Furthermore, the reaction could be scaled up to the multigram scale.

Recommanded Product: 1-(4-Nitrophenyl)ethanone. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Zhang, S; Shi, XH; Li, JC; Hou, ZT; Song, ZH; Su, XF; Peng, D; Wang, F; Yu, YT; Zhao, GL or concate me.

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem