121809-77-6

Upstream product

• 117011-70-8 2-(4-aminophenoxy)-2-methyl propionic acid 
• 41195-90-8 1,2-dichloro-3-isocyanatobenzene 
• 7159-95-7 (4-hydroxyphenyl)carbamic acid ethyl ester 
• 123-30-8 4-amino-phenol 
• 767-00-0 4-cyanophenol 
• 79925-16-9 2-(4-cyanophenoxy)-2-methylpropionic acid 
• 121809-55-0 2-<4-<(ethoxycarbonyl)amino>phenoxy>-2-methylpropionic acid 
• 121809-54-9 2-(4-carbamoylphenoxy)-2-methylpropionic acid 
• 67-66-3 chloroform 
• 67-64-1 acetone 

Relevant academic research and scientific papers

Synthesis of (+)-Turmeronol A, an Inhibitor of Soybean Lipoxygenase, and (+)-ar-Turmerone

Syntheses of optically pure turmeronol A and turmerone were achieved in a simple manner starting from ethyl (R)-3-hydroxybutanoate (4) of 100percent e.e.The key step was the displacement of the chiral tosylate (6) with an organocopper reagent.

Synthesis and Investigation of Effects of 2-amino>phenoxy>-2-methylpropionic Acids on the Affinity of Hemoglobin for Oxygen: Structure-Activity Relationships

A series of 2-carbonyl>amino>phenoxy>-2-methylpropionic acids and other substituted phenoxyacetic acids were synthesized and tested for their ability to reduce the affinity of hemoglobin for oxygen. 2-4-(3,4,5-Trichloro