1021245-67-9

Upstream product

• 34680-81-4 2-bromo-N-methylacetamide 
• 104-94-9 4-methoxy-aniline 
• 598-21-0 2-Bromoacetyl bromide 
• 74-89-5 methylamine 

Downstream Products

• 1073534-48-1 C₁₈H₁₇BrN₂O₂ 
• 1073534-47-0 C₂₄H₂₂N₂O₂ 
• 1073534-51-6 C₁₉H₂₀N₂O₃ 
• 1073534-42-5 C₁₈H₁₈N₂O₂ 
• 1073534-49-2 C₁₉H₂₀N₂O₂ 
• 1370469-93-4 4-(4-chlorophenyl)-6-methoxy-N-methylquinoline-2-carboxamide 
• 1370469-99-0 C₂₄H₂₀N₂O₂ 
• 1370469-92-3 4-(4-(tert-butyl)phenyl)-6-methoxy-N-methylquinoline-2-carboxamide 
• 1370469-90-1 6-methoxy-N-methyl-4-phenylquinoline-2-carboxamide 
• 1370469-95-6 6-methoxy-4-(4-methoxyphenyl)-N-methylquinoline-2-carboxamide 
• 1205585-34-7 C₁₀H₁₂N₂O₂ 
• 345-32-4 5-(trifluoromethyl)isatin 

Relevant academic research and scientific papers

Enantioselective synthesis of arylglycine derivatives by direct C-H oxidative cross-coupling

A new method for the synthesis of chiral α-amino acid derivatives by enantioselective C-H arylation of N-aryl glycine esters with aryl boric acids in the presence of a chiral Pd(ii)-catalyst has been developed. This work successfully integrates the direct C-H oxidation with asymmetric arylation and exhibits excellent enantioselectivity. This journal is

Phosphorylation of Glycine Derivatives via Copper(I)-Catalyzed Csp3?H Bond Functionalization

A simple and efficient one-pot approach has been developed for a copper-catalyzed phosphorylation of glycine derivatives under air and at room temperature. The present cross-dehydrogenative coupling allows various methoxyphenyl-protected glycine derivativ

Copper Triflate Catalyzed Oxidative α-Allylation of Glycine Derivatives

Copper triflate catalyzed oxidative C-H functionalization of glycine derivatives with allyltributyltin has been established using oxygen or tert -butyl hydroperoxide as oxidant. Various glycine esters and glycine amides were suitable substrates for this oxidative allylation reaction and afforded the desired homoallylic amines in moderate to good yields.

A 4 - phenyl quinoline compound, preparation method and application thereof (by machine translation)

The invention discloses a 4 - phenyl quinoline compound, its preparation method and application, the invention of the 4 - phenyl quinoline compound to, its structure (I) shown in the diimmonium: Wherein R1 Is - OH, - Cl, - OCH3 Or -

Functionalizing glycine derivatives by direct C-C bond formation

(Chemical Equation Presented) Come on glycine: Two different types of glycine derivatives are α-functionalized using cross-dehydrogenative- coupling (CDC) reactions. The method allows the efficient attachment of a malonate or aromatic alkyne group on the α-position of the glycine derivatives under very mild conditions.