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289909-44-0

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289909-44-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 289909-44-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,9,9,0 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 289909-44:
(8*2)+(7*8)+(6*9)+(5*9)+(4*0)+(3*9)+(2*4)+(1*4)=210
210 % 10 = 0
So 289909-44-0 is a valid CAS Registry Number.

289909-44-0Relevant academic research and scientific papers

Stereo- and Regiocontrolled Methylboration of Terminal Alkynes

Zhurakovskyi, Oleksandr,Dias, Rafael M. P.,Noble, Adam,Aggarwal, Varinder K.

supporting information, p. 3136 - 3139 (2018/05/28)

A scalable and operationally simple synthesis of trisubstituted alkenyl boronic esters has been achieved using a Zr-catalyzed carboalumination of terminal alkynes followed by in situ transmetalation with i-PrOBpin. The products are formed in good yields and with excellent regioselectivity and perfect stereoselectivity. The new procedure provides a significant improvement over the previously reported syntheses.

Rhodium-Catalyzed Asymmetric Synthesis of β-Branched Amides

Wu, Zhao,Laffoon, Joshua D.,Nguyen, Trang T.,McAlpin, Jacob D.,Hull, Kami L.

supporting information, p. 1371 - 1375 (2017/01/24)

A general asymmetric route for the one-step synthesis of chiral β-branched amides is reported through the highly enantioselective isomerization of allylamines, followed by enamine exchange, and subsequent oxidation. The enamine exchange allows for a rapid and modular synthesis of various amides, including challenging β-diaryl and β-cyclic.

Enantioselective synthesis of quaternary carbon stereogenic centers through copper-catalyzed conjugate additions of aryl- and alkylaluminum reagents to acyclic trisubstituted enones

Dabrowski, Jennifer A.,Villaume, Matthew T.,Hoveyda, Amir H.

supporting information, p. 8156 - 8159 (2013/08/23)

Acyclic quaternary carbons by conjugate addition: The first examples of catalytic enantioselective conjugate additions of aryl and alkyl units that generate acyclic all-carbon quaternary stereogenic centers have been developed (see scheme). The requisite

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