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GPhos is a novel class of phosphine ligands designed for catalytic applications in organic synthesis. These ligands feature a bulky, electron-rich phosphine group that enhances their ability to stabilize metal complexes and facilitate challenging chemical transformations. With their unique structure and reactivity, GPhos ligands have demonstrated potential in a range of reactions, including cross-coupling, hydrogenation, and asymmetric catalysis, making them valuable tools for synthetic chemists in constructing complex molecular structures. GPhos represents a promising advancement in the field of organometallic chemistry and catalysis.
Usage:
Used in Organic Synthesis:
GPhos is used as a phosphine ligand for enhancing the stabilization of metal complexes and facilitating challenging chemical transformations in organic synthesis.
Used in Cross-Coupling Reactions:
GPhos is used as a ligand in cross-coupling reactions to improve the efficiency and selectivity of these processes, enabling the formation of new carbon-carbon or carbon-heteroatom bonds.
Used in Hydrogenation Reactions:
GPhos is used as a ligand in hydrogenation reactions to promote the reduction of various functional groups, improving the reaction's efficiency and selectivity.
Used in Asymmetric Catalysis:
GPhos is used as a chiral ligand in asymmetric catalysis to induce enantioselectivity, enabling the synthesis of optically active compounds with high enantiomeric purity.
Used in the Development of New Synthetic Methods:
GPhos is used as a tool by synthetic chemists to explore and develop new methods for constructing complex molecular structures, advancing the field of organometallic chemistry and catalysis.

2489243-29-8

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2489243-29-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2489243-29-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 2,4,8,9,2,4 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2489243-29:
(9*2)+(8*4)+(7*8)+(6*9)+(5*2)+(4*4)+(3*3)+(2*2)+(1*9)=208
208 % 10 = 8
So 2489243-29-8 is a valid CAS Registry Number.

2489243-29-8Downstream Products

2489243-29-8Relevant academic research and scientific papers

Development of an aryl amination catalyst with broad scope guided by consideration of catalyst stability

McCann, Scott D.,Reichert, Elaine C.,Arrechea, Pedro Luis,Buchwald, Stephen L.

supporting information, p. 15027 - 15037 (2020/10/13)

We have developed a new dialkylbiaryl monophosphine ligand, GPhos, that supports a palladium catalyst capable of promoting carbon-nitrogen cross-coupling reactions between a variety of primary amines and aryl halides; in many cases, these reactions can be carried out at room temperature. The reaction development was guided by the idea that the productivity of catalysts employing BrettPhos-like ligands is limited by their lack of stability at room temperature. Specifically, it was hypothesized that primary amine and N-heteroaromatic substrates can displace the phosphine ligand, leading to the formation of catalytically dormant palladium complexes that reactivate only upon heating. This notion was supported by the synthesis and kinetic study of a putative off-cycle Pd complex. Consideration of this off-cycle species, together with the identification of substrate classes that are not effectively coupled at room temperature using previous catalysts, led to the design of a new dialkylbiaryl monophosphine ligand. An Ot-Bu substituent was added ortho to the dialkylphosphino group of the ligand framework to improve the stability of the most active catalyst conformer. To offset the increased size of this substituent, we also removed the para i-Pr group of the non-phosphorus-containing ring, which allowed the catalyst to accommodate binding of even very large α-tertiary primary amine nucleophiles. In comparison to previous catalysts, the GPhos-supported catalyst exhibits better reactivity both under ambient conditions and at elevated temperatures. Its use allows for the coupling of a range of amine nucleophiles, including (1) unhindered, (2) five-membered-ring N-heterocycle-containing, and (3) α-tertiary primary amines, each of which previously required a different catalyst to achieve optimal results.

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