40934-39-2

Upstream product

• 42069-18-1 C₁₆H₁₂Cl₂O₃ 
• 108-91-8 cyclohexylamine 
• 57217-54-6 N-hydroxy-N-cyclohexylphenylacetamide 
• 143217-10-1 N-(mesyloxy)-N-cyclohexylphenylacetamide 
• 25100-12-3 N-cyclohexylhydroxylamine hydrochloride 
• 103-80-0 phenylacetyl chloride 
• 4755-72-0 Chloro-phenyl-acetic acid 

Downstream Products

• 40934-43-8 N-(α-Cyclohexylcarbamoylbenzyl)-glycinethylester 
• 39691-28-6 cyclohexyl-(2-morpholin-4-yl-2-phenyl-ethyl)-amine 
• 39691-29-7 N-cyclohexyl-2-morpholin-4-yl-2-phenyl-acetamide 

Relevant academic research and scientific papers

Lewis acid-catalyzed formation of Ugi four-component reaction product from Passerini three-component reaction system without an added amine

In the presence of a Lewis acid the phenol-Passerini three-component reaction (phenol-P-3CR) system is found to deliver a product of the phenol-Ugi four-component reaction (phenol-U-4CR). It is the first demonstration of an isocyanide as an amine equivale

Base-Promoted Reaction of O-Sulfonylated Hydroxamic Acids with Nucleophiles. A New Mehtod for the Synthesis of α-Substituted Amides

Treatment of a series of hydroxamic acids 2 with mesyl chloride in the presence of 2 equiv of triethylamine at 0 deg C gives 2-chloroamides 3 in good yields.Use of a single equivalent of triethylamine gives the N-(mesyloxy)amides 1, which are versatile sy