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(3R)-3-[(1S)-1-(4-bromo-phenyl)-2-nitro-ethyl]-3-methyl-2-oxo-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1169769-85-0

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1169769-85-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1169769-85-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,9,7,6 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1169769-85:
(9*1)+(8*1)+(7*6)+(6*9)+(5*7)+(4*6)+(3*9)+(2*8)+(1*5)=220
220 % 10 = 0
So 1169769-85-0 is a valid CAS Registry Number.

1169769-85-0Downstream Products

1169769-85-0Relevant academic research and scientific papers

Diastereodivergent Asymmetric 1,4-Addition of Oxindoles to Nitroolefins by Using Polyfunctional Nickel-Hydrogen-Bond-Azolium Catalysts

Mechler, Melanie,Peters, Ren

supporting information, p. 10303 - 10307 (2015/09/01)

Diastereodivergency is a challenge for catalytic asymmetric synthesis. For many reaction types, the generation of one diastereomer is inherently preferred, while the other diastereomers are not directly accessible with high efficiency and require circuitous synthetic approaches. Overwriting the inherent preference by means of a catalyst requires control over the spatial positions of both reaction partners. We report a novel polyfunctional catalyst type in which a NiII-bis(phenoxyimine) unit, free hydroxy groups, and an axially chiral bisimidazolium entity participate in the stereocontrol of the direct 1,4-addition of oxindoles to nitroolefins. Both epimers of the 1,4-adduct are accessible in excess on demand by changes to the ligand constitution and configuration. As the products have been reported to be valuable precursors to indole alkaloids, this method should allow access to their epimeric derivatives.

Squaramide-catalyzed diastereo- and enantioselective Michael addition of 3-substituted oxindoles to nitroalkenes

Yang, Wen,Wang, Jingsi,Du, Da-Ming

experimental part, p. 972 - 980 (2012/09/22)

An efficient diastereo- and enantioselective Michael addition of 3-substituted oxindoles onto nitroalkenes catalyzed by a bifunctional chiral squaramide catalyst has been developed. This organocatalytic reaction with 2 mol % of catalyst proceeded smoothly

A homodinuclear Mn(III)2-Schiff base complex for catalytic asymmetric 1,4-additions of oxindoles to nitroalkenes

Kato, Yuko,Furutachi, Makoto,Chen, Zhihua,Mitsunuma, Harunobu,Matsunaga, Shigeki,Shibasaki, Masakatsu

supporting information; experimental part, p. 9168 - 9169 (2009/12/06)

(Chemical Equation Presented) Catalytic asymmetric 1,4-additions of 3-substituted oxindoles to β-aryl, β-heteroaryl, and β-alkenyl nitroalkenes are described. A new homodinuclear Mn2(OAc) 2-Schiff base 1 complex was required to reali

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