33720-38-6

Upstream product

• 186581-53-3 diazomethane 
• 99843-30-8 1-(4-hydroxyphenyl)-3-methylpyrrolidine-2,5-dione 
• 109933-71-3 1-(4-methoxy-phenyl)-5-(4-methoxy-phenylimino)-3-methyl-pyrrolidin-2-one 
• 133505-00-7 (2R*,3R*)-1-(4-methoxyphenyl)-3-methyl-4-oxoazetidine-2-carbaldehyde 
• 104-94-9 4-methoxy-aniline 
• 76738-06-2 1-(4-methoxyphenyl)-3-methyl-1H-pyrrole-2,5-dione 
• 616-02-4 citraconic acid anhydride 
• 109566-12-3 N-(4-hydroxy-phenyl)-3-methyl-succinomonoimidic acid-1-(4-hydroxy-anilide) 
• 24978-42-5 (E,E)-N¹,N²-bis(4-methoxyphenyl)ethane-1,2-diimine 
• 498-21-5 2-methylbutanedioic acid 

Relevant academic research and scientific papers

Experimental and theoretical study on the structure-property relationship of novel 1-aryl-3-methylsuccinimides

A series of ten 1-aryl-3-methylsuccinimides was synthesized and their solvatochromic properties were studied in a set of fifteen binary solvent mixtures. The solute-solvent interactions were analyzed on the basis of the linear solvation energy relationshi

Effects of chirality on the antifungal potency of methylated succinimides obtained by Aspergillus fumigatus biotransformations. Comparison with racemic ones

Eighteen (3R) and (3R,4R)-N-phenyl-, N-phenylalkyl and N-arylsuccinimides were prepared with high enantioselectivity by biotransformation of maleimides with A. fumigatus. This environmentally friendly, clean and economical procedure was performed by the w

N-heterocyclic carbene catalyzed ring expansion of 4-formyl-β-lactams: Synthesis of succinimide derivatives

N-Heterocyclic carbene (NHC) has been employed as an efficient catalyst for ring expansion of 4-formyl-β-lactams, allowing the facile synthesis of succinimide derivatives. This organocatalytic process features readily availability of the catalyst, low cat