What I Wish Everyone Knew About 1-(4-Nitrophenyl)ethanone

About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Zhang, GQ; Zeng, HS; Li, SH; Johnson, J; Mo, ZX; Neary, MC; Zheng, SP or concate me.. Application In Synthesis of 1-(4-Nitrophenyl)ethanone

An article 1-D manganese(ii)-terpyridine coordination polymers as precatalysts for hydrofunctionalisation of carbonyl compounds WOS:000517990300024 published article about MAGNESIUM-CATALYZED HYDROBORATION; ASYMMETRIC TRANSFER HYDROGENATION; SELECTIVE HYDROBORATION; ALDEHYDES; KETONES; HYDROSILYLATION; REDUCTION; COMPLEXES; EFFICIENT; IRON(II) in [Zhang, Guoqi; Zeng, Haisu; Li, Sihan; Johnson, Jahvon; Mo, Zixuan] CUNY, Grad Ctr, Dept Sci, John Jay Coll, New York, NY 10019 USA; [Zhang, Guoqi; Zeng, Haisu; Li, Sihan; Johnson, Jahvon; Mo, Zixuan] CUNY, Grad Ctr, PhD Program Chem, New York, NY 10019 USA; [Zeng, Haisu; Li, Sihan; Neary, Michelle C.; Zheng, Shengping] CUNY Hunter Coll, Dept Chem, New York, NY 10065 USA in 2020.0, Cited 60.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6. Application In Synthesis of 1-(4-Nitrophenyl)ethanone

Reductive catalysis with earth-abundant metals is currently of increasing importance and shows potential in replacing precious metal catalysis. In this work, we revealed catalytic hydroboration and hydrosilylation of ketones and aldehydes achieved by a structurally defined manganese(ii) coordination polymer (CP) as a precatalyst under mild conditions. The manganese-catalysed methodology can be applied to a range of functionalized aldehydes and ketones with turnover numbers (TON) of up to 990. Preliminary results on the regioselective catalytic hydrofunctionalization of styrenes by the Mn-CP catalyst are also presented.

About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Zhang, GQ; Zeng, HS; Li, SH; Johnson, J; Mo, ZX; Neary, MC; Zheng, SP or concate me.. Application In Synthesis of 1-(4-Nitrophenyl)ethanone

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