2306-53-8

Upstream product

• 4870-65-9 2-bromophenylacetic acid 
• 108-91-8 cyclohexylamine 
• 25100-12-3 N-cyclohexylhydroxylamine hydrochloride 
• 103-80-0 phenylacetyl chloride 
• 57217-54-6 N-hydroxy-N-cyclohexylphenylacetamide 
• 19078-72-9 bromo(phenyl)acetyl chloride 
• 143217-10-1 N-(mesyloxy)-N-cyclohexylphenylacetamide 

Relevant academic research and scientific papers

Arylglycinamide derivatives and preparative processes therefor

Arylglycinamide derivatives represented by a general formula (1) STR1 (wherein Ar denotes a phenyl group which may have 1 to 3 substituents or naphthyl group which may have 1 to 3 substituents, R1 and R4 denote identically or differe

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

Synthesis of new alpha-hydrazinoarylacetic acids and derivatives.

The synthesis of some alpha-hydrazinoarylacetic acids (I) by reaction of alpha-bromoarylacetic acids with hydrazine, alkylhydrazines and carbobenzyloxyhydrazines is described. Reduction of the hydrazones of 2- and 3-thienylglyoxylic acids provided a gener