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(2R,2'R)-2,2'-((2-iodo-1,3-phenylene)bis(oxy))bis(1-(piperidin-1-yl)propan-1-one) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1611494-91-7

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1611494-91-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1611494-91-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,1,4,9 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1611494-91:
(9*1)+(8*6)+(7*1)+(6*1)+(5*4)+(4*9)+(3*4)+(2*9)+(1*1)=157
157 % 10 = 7
So 1611494-91-7 is a valid CAS Registry Number.

1611494-91-7Downstream Products

1611494-91-7Relevant academic research and scientific papers

Chiral Aryliodine-Mediated Enantioselective Organocatalytic Spirocyclization: Synthesis of Spirofurooxindoles via Cascade Oxidative C-O and C-C Bond Formation

Cao, Yang,Zhang, Xiang,Lin, Guangyu,Zhang-Negrerie, Daisy,Du, Yunfei

, p. 5580 - 5583 (2016)

An enantioselective organocatalytic oxidative spirocyclization of alkyl 3-oxopentanedioate monoamide derivatives leading to the formation of diverse spirofurooxindoles with high enantioselectivity has been realized via chiral aryliodine-mediated cascade C-O and C-C bond formations. The reaction is postulated to proceed via oxidative C-O bond formation followed by oxidative C-C bond formation, with the latter being the enantioselectivity-determining step.

Catalytic Asymmetric Diamination of Styrenes

Mu?iz, Kilian,Barreiro, Laura,Romero, R. Martín,Martínez, Claudio

supporting information, p. 4354 - 4357 (2017/04/04)

An enantioselective catalytic vicinal diamination of styrenes is reported, which proceeds under entirely intermolecular reaction control. It relies on a chirally modified aryliodine(I) catalyst and proceeds within an iodine(I/III) manifold with conventional 3-chloroperbenzoic acid as a terminal oxidant. An environmentally benign solvent combination not only adds to the attractiveness of the process but also slows down the rate of the undesired background reaction. A total of 30 examples are presented, which consistently provide high enantiomeric excesses in the range 91-98%.

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