93953-53-8

Upstream product

• 14224-99-8 2-methyl-4,5-diphenyloxazole 
• 83665-55-8 2-(2-iodoethyl)-1,3-dioxolane 
• 18742-02-4 2-bromo-2-(2-ethyl)dioxolane 

Downstream Products

• 93953-54-9 (E)-6-(4,5-Diphenyl-oxazol-2-yl)-hex-2-enoic acid methyl ester 
• 93967-85-2 {(2R,3R)-3-[3-(4,5-Diphenyl-oxazol-2-yl)-propyl]-oxiranyl}-methanol 
• 93953-55-0 (E)-6-(4,5-Diphenyl-oxazol-2-yl)-hex-2-en-1-ol 
• 91621-02-2 2-(4-oxobutyl)-4,5-diphenyloxazole 

Relevant academic research and scientific papers

ASYMMETRIC EPOXIDATION OF ALLYLIC ALCOHOLS EMPLOYING 4,5-DIPHENYLOXAZOLE AS A MASKED ESTER FUNCTIONALITY

The 4,5-diphenyloxazolyl moiety has been found to be a masked ester functionality fully compatible with the Sharpless epoxidation of allylic alcohols within the same molecule.

Synthesis of 1,2-Polymethyleneimidazoles Utilizing Intramolecular Ring Transformation

Among the intramolecular cyclodehydration of 2-(β-, δ-, and ε-aminoalkyl)oxazoles, 2-(δ-aminoalkyl)oxazoles afforded the desired 1,2-tetramethyleneimidazoles on pyrolysis, while 2-(β- and ε-aminoalkyl)oxazoles unchanged under the same conditions.