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Tris(2-methoxyphenyl)-1,3,5,2,4,6-trioxatriborinane is a complex organic compound with the molecular formula C18H15B3O6. It is a derivative of borinane, a boron-containing heterocycle, and features three 2-methoxyphenyl groups attached to the boron atoms. tris(2-methoxyphenyl)-1,3,5,2,4,6-trioxatriborinane is known for its potential applications in organic synthesis, particularly as a Lewis acid catalyst. It can facilitate various chemical reactions, such as the formation of carbon-carbon bonds, due to its ability to accept electron pairs and stabilize intermediates. The presence of the methoxy groups on the phenyl rings can influence the electronic properties and reactivity of the compound, making it a versatile tool in the hands of chemists.

79422-01-8

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79422-01-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79422-01-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,4,2 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 79422-01:
(7*7)+(6*9)+(5*4)+(4*2)+(3*2)+(2*0)+(1*1)=138
138 % 10 = 8
So 79422-01-8 is a valid CAS Registry Number.

79422-01-8Relevant academic research and scientific papers

Oxidative coupling of aryl boron reagents with sp3-carbon nucleophiles: The enolate chan–evans–lam reaction

Moon, Patrick J.,Halperin, Heather M.,Lundgren, Rylan J.

, p. 1894 - 1898 (2016)

Reported is a versatile new oxidative method for the arylation of activated methylene species. Under mild reaction conditions (RT to 40°C), Cu(OTf)2mediates the selective coupling of functionalized aryl boron species with a variety of stabilized sp3-nucleophiles. Tertiary malonates and amido esters can be employed as substrates to generate quaternary centers. Complementing either traditional cross-coupling or SNAr protocols, the transformation is chemoselective in the presence of halogen electrophiles, including aryl bromides and iodides. Substrates bearing amide, sulfonyl, and phosphonyl groups, which are not amenable to coupling under mild Hurtley-type conditions, are suitable reaction partners.

Highly Enantioselective Ferrocenyl Palladacycle-Acetate Catalysed Arylation of Aldimines and Ketimines with Arylboroxines

Schrapel, Carmen,Frey, Wolfgang,Garnier, Delphine,Peters, René

supporting information, p. 2448 - 2460 (2017/02/23)

Benzylic N-substituted stereocenters constitute a frequent structural motif in drugs. Their highly enantioselective generation is hence of technical importance. An attractive strategy is the arylation of imines with organoboron reagents. Chiral Rh complexes have reached a high level of productivity for this reaction type. In this article we describe that an electron rich PdIIcatalyst also performs well in the arylation of aldimines, comparable to the best Rh catalysts. The ferrocenyl palladacycle-acetate catalyst allows for a broad substrate scope and very high enantioselectivities. Commonly observed side reactions like aryl–aryl homocouplings and imine hydrolysis could be blocked. Mechanistic studies implicate that a) the acetate ligand is crucial for transmetallation, b) the active catalyst is most likely a palladacycle-OAc monomer, c) the rate limiting step is probably the product release. By added KOAc the arylation could also be applied to ketimines.

Mild and ligand-free Pd(II)-catalyzed conjugate additions to hindered γ-substituted cyclohexenones

Jordan-Hore, James A.,Sanderson, James N.,Lee, Ai-Lan

supporting information; scheme or table, p. 2508 - 2511 (2012/07/03)

Ligand-free cationic Pd(II) catalyst with NaNO3 as an additive is a highly active catalytic system for conjugate additions to sterically hindered γ-substituted cyclohexenones. More challenging γγ- and βγ-substrates also react well to produce products with quaternary centers in good dr. The conjugate additions occur in a diastereoselective fashion under mild, practical and air-stable conditions, using readily available commercial reagents.

Bis-sulfamyl imines: Potent substrates for asymmetric additions of arylboroxines under rhodium catalysis

Crampton, Rosemary,Woodward, Simon,Fox, Martin

supporting information; experimental part, p. 903 - 906 (2011/06/19)

Bis-sulfamyl imines are shown to be potentially ideal substrates for rhodium-catalysed asymmetric additions of arylboron nucleophiles as they show: (i) near perfect enantioselectivities (11 examples, 98-99+% ee), (ii) good to excellent diastereoselectivities (10-32:1 rac:meso), and (iii) high functional group tolerance in removal of the low molecular weight protecting group via mild heating in aqueous pyridine.

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