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69060-18-0

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69060-18-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69060-18-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,0,6 and 0 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 69060-18:
(7*6)+(6*9)+(5*0)+(4*6)+(3*0)+(2*1)+(1*8)=130
130 % 10 = 0
So 69060-18-0 is a valid CAS Registry Number.

69060-18-0Relevant articles and documents

Nickel-Catalyzed Asymmetric Reductive 1,2-Carboamination of Unactivated Alkenes

He, Jun,Xue, Yuhang,Han, Bo,Zhang, Chunzhu,Wang, You,Zhu, Shaolin

supporting information, p. 2328 - 2332 (2020/01/08)

Starting from diverse alkene-tethered aryl iodides and O-benzoyl-hydroxylamines, the enantioselective reductive cross-electrophilic 1,2-carboamination of unactivated alkenes was achieved using a chiral pyrox/nickel complex as the catalyst. This mild, modular, and practical protocol provides rapid access to a variety of β-chiral amines with an enantioenriched aryl-substituted quaternary carbon center in good yields and with excellent enantioselectivities. This process reveals a complementary regioselectivity when compared to Pd and Cu catalysis.

Catalytic, enantioselective, and highly chemoselective bromocyclization of olefinic dicarbonyl compounds

Zhao, Yi,Jiang, Xiaojian,Yeung, Ying-Yeung

supporting information, p. 8597 - 8601 (2013/09/12)

Overriding preferences: An amine-thiocarbamate catalyst can mediate the facile, efficient, and highly enantioselective bromocyclization of olefinic 1,3-dicarbonyl compounds. In the presence of the bifunctional catalyst, the bromination occurs chemoselectively at the olefinic moiety rather than at the carbon atom in the α-position to the carbonyl units. Copyright

Nazarov-type reactions in water

Kokubo, Masaya,Kobayashi, Shu

supporting information; experimental part, p. 526 - 528 (2010/04/23)

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