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bis(4-(methoxycarbonyl)phenyl)iodonium tetrafluoroborate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1426243-57-3

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1426243-57-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1426243-57-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,6,2,4 and 3 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1426243-57:
(9*1)+(8*4)+(7*2)+(6*6)+(5*2)+(4*4)+(3*3)+(2*5)+(1*7)=143
143 % 10 = 3
So 1426243-57-3 is a valid CAS Registry Number.

1426243-57-3Relevant academic research and scientific papers

Aniline carbamates: A versatile and removable motif for palladium-catalyzed directed c-h activation

Uhlig, Nick,Li, Chao-Jun

, p. 12066 - 12070 (2014)

The aniline carbamate is introduced as a new removable directing group for C-H activation. Its versatility and ability as a directing group are demonstrated by its use in the ortho-arylation of a wide variety of aniline derivatives under palladium(II) catalysis, with symmetric diaryliodonium salts as aryl donors. The reaction differs from previously reported arylations in its selectivity and its mechanism, as elucidated by kinetic and isotopic experiments. The directing group can also be easily removed under a variety of conditions.

Spatial anion control on palladium for mild C-H arylation of arenes

Dhankhar, Jyoti,González-Fernández, Elisa,Dong, Chao-Chen,Mukhopadhyay, Tufan K.,Linden, Anthony,?ori?, Ilija

supporting information, p. 19040 - 19046 (2020/11/13)

C-H arylation of arenes without the use of directing groups is a challenge, even for simple molecules, such as benzene. We describe spatial anion control as a concept for the design of catalytic sites for C-H bond activation, thereby enabling nondirected C-H arylation of arenes at ambient temperature. The mild conditions enable late-stage structural diversification of biologically relevant small molecules, and site-selectivity complementary to that obtained with other methods of arene functionalization can be achieved. These results reveal the potential of spatial anion control in transition-metal catalysis for the functionalization of C-H bonds under mild conditions.

Iron-catalyzed synthesis of arylsulfinates through radical coupling reaction

Zhang, Weixi,Luo, Meiming

supporting information, p. 2980 - 2983 (2016/02/19)

A novel strategy for installation of a sulfonyl fragment into arenes has been accomplished via an iron-catalyzed radical coupling reaction. Arene radicals derived from diaryliodoniums via single electron transfer reaction combine with sulfoxylate anion radicals readily generated from commercially available rongalite (HOCH2SO2Na·2H2O) to afford arylsulfinates efficiently at room temperature. In this protocol, a broad range of functional groups are tolerated to give products in good yields.

Palladium-catalyzed arylation of simple arenes with iodonium salts

Storr, Thomas E.,Greaney, Michael F.

supporting information, p. 1410 - 1413 (2013/05/09)

The development of an arylation protocol for simple arenes with diaryliodonium salts using the Herrmann-Beller palladacycle catalyst is reported. The reaction takes simple aromatic feedstocks and creates valuable biaryls for use in all sectors of the chem

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