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1-(4-bromophenyl)ethan-1-one O-pivaloyl oxime is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1570194-60-3

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1570194-60-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1570194-60-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,7,0,1,9 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1570194-60:
(9*1)+(8*5)+(7*7)+(6*0)+(5*1)+(4*9)+(3*4)+(2*6)+(1*0)=163
163 % 10 = 3
So 1570194-60-3 is a valid CAS Registry Number.

1570194-60-3Relevant academic research and scientific papers

Methyl ketone oxime esters as nucleophilic coupling partners in Pd-catalyzed C-H alkylation and application in the synthesis of isoquinolines

Zhang, Zhi-Wei,Lin, Aijun,Yang, Jiong

, p. 7041 - 7050 (2014)

Methyl ketone oxime esters have been found to be excellent coupling partners for C(sp2)-C(sp3) bond formation via Pd-catalyzed aromatic C-H activation. This transformation forms the basis of an approach to regioselectively synthesize substituted isoquinolines via coupling with aryloxime esters. Our mechanistic studies suggested that the reaction proceeded through Pd(II)-catalyzed aromatic C-H activation, tautomerization, and a 1,3-shift of the palladacycle-ligated methyl ketone oxime ester to enable the C-C bond formation by reductive elimination, and intramolecular condensation of an imido-Pd(II) intermediate to form the heterocycle. The aryloxime group not only was used as a directing group for Pd-catalyzed aromatic C-H activation but also functioned as an internal oxidant to allow the reaction to be redox-neutral. Our study illuminated the scope and limitations of this C-H alkylation process, which may serve as the point of departure for developing other C-H functionalization reactions using oxime esters and potentially other carbonyl derivatives as the nucleophilic coupling partners.

Rhodium(iii)-catalyzed asymmetric [4+1] spiroannulations of: O -pivaloyl oximes with α-diazo compounds

Chang, Junbiao,Deng, Wei-Qiao,Kong, Lingheng,Li, Xingwei,Liu, Bingxian,Sun, Lincong,Wang, Fen,Zhao, Yanlian

supporting information, p. 8268 - 8271 (2021/08/25)

Chiral RhIII catalysts can catalyze the asymmetric [4+1] spiroannulation of O-pivaloyl oximes with α-diazo homophthalimides under redox-neutral and acid/base-neutral conditions, leading to formation of chiral spirocyclic imines as a result of C-H activation and N-O cleavage. The reaction proceeded with high efficiency and features broad substrate scope, mild reaction conditions, and high to excellent enantioselectivities. This journal is

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