38430-05-6

Upstream product

• 33993-35-0 cis-benzylideneaniline 
• 93-98-1 N-phenyl benzoyl amide 
• 98-88-4 benzoyl chloride 
• 62-53-3 aniline 

Downstream Products

• 62302-16-3 5-amino-2,3-diphenyl-[1,2,4]thiadiazolium; chloride 
• 98888-67-6 Phenyl-thiobenzoyl-thiocarbamic acid O-methyl ester 
• 98888-68-7 phenyl-thiobenzoyl-thiocarbamic acid O-ethyl ester 
• 98888-69-8 Phenyl-thiobenzoyl-thiocarbamic acid O-propyl ester 
• 62302-12-9 2,3,5,6-tetraphenyl-3,5-dihydro-4λ⁴-[1,2,4]thiadiazolo[5,1-e][1,2,4]thiadiazole 
• 93-98-1 N-phenyl benzoyl amide 
• 3393-96-2 p-nitrobenzanilide 
• 728-90-5 N-(2-nitrophenyl)benzanilide 
• 4073-72-7 3,4,5-triphenyl-1,2,4-triazole 
• 143826-23-7 2,5-diphenyl-3H-1,3,4-benzotriazepine 
• 206360-80-7 N-Phenyl-benzimidic acid (E)-hex-2-enyl ester 
• 334026-33-4 1-phenylimino-1-phenyl-2-butyne 
• 854016-59-4 N-(phenyl-phenylimino-methyl)-benzamidine 
• 837-56-9 1-phenyl-2-phenylpyrrole 

Relevant academic research and scientific papers

Sterically hindered (pyridyl)benzamidine palladium(II) complexes: Syntheses, structural studies, and applications as catalysts in the methoxycarbonylation of olefins

Reactions of ligands (E)-N′-(2,6-diisopropylphenyl)-N-(4-methylpyridin-2-yl)benzimidamide (L1), (E)-N′-(2,6-diisopropylphenyl)-N-(6-methylpyridin-2-yl)benzimidamide (L2), (E)-N′-(2,6-dimethylphenyl)-N-(6-methylpyridin-2-yl)benzimidamide (L3), (E)-N′-(2,6-dimethylphenyl)-N-(4-methylpyridin-2-yl)benzimidamide (L4), and (E)-N-(6-methylpyridin-2-yl)-N′-phenylbenzimidamide (L5) with [Pd(NCMe)2Cl2] furnished the corresponding palladium(II) precatalysts (Pd1–Pd5), in good yields. Molecular structures of Pd2 and Pd3 revealed that the ligands coordinate in a N^N bidentate mode to afford square planar compounds. Activation of the palladium(II) complexes with para-tolyl sulfonic acid (PTSA) afforded active catalysts in the methoxycarbonylation of a number of alkene. The resultant catalytic activities were controlled by the both the complex structure and alkene substrate. While aliphatic substrates favored the formation of linear esters (>70%), styrene substrate resulted in the formation of predominantly branched esters of up to 91%.

Quest for Efficient Catalysts based on Zinc tert-Butyl Peroxides for Asymmetric Epoxidation of Enones: C2- vs C1-Symmetric Auxiliaries

Zinc tert-butyl peroxide-based catalysts for the asymmetric epoxidation of enones using tert-butyl hydroperoxide as an oxidant have been developed. A comparative study of chiral monoanioninc N,N′-bidentate ligands, C2-symmetric bisoxazolinates and C1-symmetric enaminooxazolinates, revealed excellent performance of C1-symmetric auxiliary ligands on catalytic asymmetric epoxidation of enones (up to 96% yield, 91% ee).

Non-steroidal anti-inflammatory agents, Part 19. E-2-pyrrolizin-5-yl acrylic acids as potent dual or selective inhibitors of bovine cyclooxygenase and 5-lipoxygenase.

The pyrrolizinyl substituted acrylic acid derivatives represent another class of dual and selective inhibitors of cyclooxygenase and 5-lipoxygenase. By modifying their substitution pattern at the phenyl moiety of C-6 the balance between the activity again