5359-48-8

Upstream product

• 67-56-1 methanol 
• 21771-89-1 α-(4-bromophenyl)phenylacetic acid 
• 264881-99-4 methyl 2-(4-bromophenyl)-2-diazoacetate 
• 98-80-6 phenylboronic acid 
• 1878-68-8 2-(4-bromophenyl)-acetic acid 
• 41841-16-1 (4-bromo-phenyl)-acetic acid methyl ester 
• 934-56-5 trimethyl(phenyl)stannane 
• 2996-92-1 phenyl trimethylsiloxane 
• 1070671-69-0 2-(4-bromophenyl)-2-phenyloxirane 
• 75195-67-4 C₁₄H₁₃BrO 
• 90-90-4 (4-bromophenyl)(phenyl)methanone 
• 33268-46-1 2-(4-bromophenyl)-2-phenylacetonitrile 
• 13391-38-3 4-bromo-benzhydryl chloride 
• 29334-16-5 phenyl(4-bromophenyl)methanol 

Downstream Products

• 1070671-74-7 methyl 2-(4'-methoxybiphenyl-4-yl)-2-phenylacetate 
• 1070671-77-0 methyl 2-phenyl-2-(4-(3-(1,1-dioxidothiomorpholin-4-yl)prop-1-ynyl)phenyl)acetate 
• 1070671-83-8 methyl 2-phenyl-2-(4-(4-(pyrimidin-2-yl)piperazin-1-yl)phenyl)acetate 
• 1423701-90-9 C₂₁H₁₇BrO₂ 
• 1423689-30-8 C₃₄H₂₉ClN₂O₅ 
• 1423689-33-1 C₃₃H₂₇ClN₂O₅ 
• 1428526-76-4 2-(4-(diethoxyphosphoryl)phenyl)-2-phenylacetic acid 
• 1428526-77-5 diethyl 4-(2-(4-hydroxy-2-(1H-pyrazol-1-yl)pyrimidine-5-ylamino)-2-oxo-1-phenylethyl)phenylphosphonate 
• 1428526-75-3 diethyl 4-[(methoxycarbonyl)(phenyl)methyl]phenylphosphonate 
• 1423700-11-1 methyl 2-phenyl-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetate 

Relevant academic research and scientific papers

Room Temperature Coupling of Aryldiazoacetates with Boronic Acids Enhanced by Blue Light Irradiation

A visible-light-promoted photochemical protocol is reported for the coupling of aryldiazoacetates with boronic acids. This photochemical reaction shows great enhancement compared to the same protocol performed in the absence of light. Except for a few cases, the room temperature coupling in the dark (thermal process) generally does not work. When it does, it is likely to also involve free carbenes as key intermediates. Alternatively, photochemical reactions show a broad scope, can be performed under air and tolerate a wide variety of functional groups. Reaction-evolution monitoring, DFT calculations and control experiments have been used to evaluate the main aspects of this intricate mechanistic scenario. Biologically active molecules Adiphenine, Benactyzine and Aprophen have been prepared as examples of synthetic applications.

RhI-Catalyzed Stille-Type Coupling of Diazoesters with Aryl Trimethylstannanes

A RhI-catalyzed cross-coupling of diazoester with arylstannane was developed. This reaction represents the first Stille-type coupling that uses a diazo compound as the coupling partner. The reaction is operationally simple and can be carried out under mild conditions, thus providing an alternative approach for the synthesis of α-aryl esters. RhI-carbene migratory insertion process is suggested to be involved as the key step in this Stille-type coupling.

Rh(I)-catalyzed cross-coupling of α-diazoesters with arylsiloxanes

An Rh(I)-catalyzed cross-coupling of diazoesters with arylsiloxanes has been successfully achieved. This transformation is a new method for the construction of the C(sp3)-C(sp2) bond, thus providing an alternative synthesis of α-aryl esters. Rh(I)-carbene migratory insertion has been proposed to be involved in this coupling reaction. The reaction represents the first example of utilizing arylsiloxane as the coupling partner in the carbene-involved cross-coupling reactions.

SUBSTITUTED PYRIMIDINES

Disclosed are substituted pyrimidines useful as HIF prolyl hydroxylase inhibitors to treat anemia and like conditions.

SUBSTITUTED PYRIMIDINES

The present invention relates to substituted pyrimidines useful as HIF prolyl hydroxylase inhibitors to treat anemia and like conditions.

LYSOPHOSPHATIDIC ACID RECEPTOR ANTAGONISTS

Compounds, methods of making such compounds, pharmaceutical compositions and medicaments comprising such compounds, and methods of using such compounds to treat, prevent or diagnose diseases, disorders, or conditions associated with one or more of the lysophosphatidic acid receptors are provided.

Carbon-carbon bond-forming reactions of α-carbonyl carbocations: Exploration of a reversed-polarity equivalent of enolate chemistry

Carbon-carbon bond-forming reactions of putative α-carbonyl carbocation intermediates generated by Lewis acid- or silver-promoted ionizations of toluenesulfonate or halide leaving groups are described. This under-exploited mode of reactivity represents an 'umpolung' of conventional enolate chemistry, and enables C-C bond construction in both intra- and intermolecular contexts. Attempts to develop diastereoselective variants of this process using chiral ester and oxazolidinone-based auxiliaries are discussed.

Arylation and vinylation of α-diazocarbonyl compounds with boroxines

An alternative approach for α-arylation and α-vinylation of carbonyl compounds is described: reaction between aryl-or vinylboroxines with α-diazocarbonyl compounds leads to the formation of α-arylated or α-vinylated carbonyl compounds under mild conditions.

INHIBITORS OF HISTONE DEACETYLASE

This invention relates to compounds for the inhibition of histone deacetylase. More particularly, the invention provides for compounds of formula compounds of the Formula (I) and N-oxides, hydrates, solvates, pharmaceutically acceptable salts, prodrugs and complexes thereof, and racemic and scalemic mixtures, diastereomers and enantiomers thereof, wherein groups L, M, X and Y are as defined herein.